Genome-wide transcript expression analysis reveals major chickpea and lentil genes associated with plant branching

The search for elite cultivars with better architecture has been a demand by farmers of the chickpea and lentil crops, which aims to systematize their mechanized planting and harvesting on a large scale. Therefore, the identification of genes associated with the regulation of the branching and architecture of these plants has currently gained great importance. Herein, this work aimed to gain insight into transcriptomic changes of two contrasting chickpea and lentil cultivars in terms of branching pattern (little versus highly branched cultivars). In addition, we aimed to identify candidate genes involved in the regulation of shoot branching that could be used as future targets for molecular breeding. The axillary and apical buds of chickpea cultivars Blanco lechoso and FLIP07–318C, and lentil cultivars Castellana and Campisi, considered as little and highly branched, respectively, were harvested. A total of 1,624 and 2,512 transcripts were identified as differentially expressed among different tissues and contrasting cultivars of chickpea and lentil, respectively. Several gene categories were significantly modulated such as cell cycle, DNA transcription, energy metabolism, hormonal biosynthesis and signaling, proteolysis, and vegetative development between apical and axillary tissues and contrasting cultivars of chickpea and lentil. Based on differential expression and branching-associated biological function, ten chickpea genes and seven lentil genes were considered the main players involved in differentially regulating the plant branching between contrasting cultivars. These collective data putatively revealed the general mechanism and high-effect genes associated with the regulation of branching in chickpea and lentil, which are potential targets for manipulation through genome editing and transgenesis aiming to improve plant architecture.


Introduction
Chickpea (Cicer arietinum L.) and lentil (Lens culinaris Medik.) are remarkable pulse crops (Fabaceae family) of outstanding importance for human consumption as sources of vegetable proteins for several European and Asian countries (Landi et al., 2021;Karalija et al., 2022).The chickpea is a self-pollinated diploid, annual-perennial, and dicotyledon, semi-erect, with a genome size estimated in 738 Mb organized in sixteen chromosomes (2n = 2x = 16) and 28,200 annotated genes (Varshney et al., 2013).In turn, lentil is a self-pollinated diploid (2n = 2x = 14), annual, and dicotyledonous, semi-erect, with a genome size estimated in 3.69 Gb organized in fourteen chromosomes and 58,243 annotated genes (Ramsay et al., 2021).To date, several germplasm banks worldwide with a high number of accessions, genotypes, lines, and commercial cultivars are available for these crops.However, there is an enormous genotypic and phenotypic variability among these genetic materials, being that the majority of these cultivars have a high number of non-dominant lateral branching and few branches with dominant growth and erect stem (Cici et al., 2008;Singh et al., 2019;Liber et al., 2021).These intrinsic agronomic characteristics need to be improved since nowadays typical chickpea and lentil cultivars have a highly complex architecture for open-field management, making mechanical harvesting difficult and increasing lodging and susceptibility to biotic and abiotic stresses (Silva-Perez et al., 2022;Tripathi et al., 2022).
The increasing and severe climate change and demand for healthy food in sufficient quantity are major factors that are challenging agriculture and consumer populations around the world (Arif et al., 2021;Grossi-de-Sa and Basso, 2024;Basso et al., 2024b).Given this, it is urgent to spend breeding efforts to improve the agronomic traits of these crops associated with abiotic and biotic tolerance, grain yield, nutritional features, and plant architecture to produce more food at a lower cost per area (Weller and Ortega, 2015;Haile et al., 2021;Asati et al., 2022;Basso et al., 2023).In particular, a significant effort still needs to be made to develop more adapted cultivars to enhance the mechanization of planting and harvesting systems (Yang et al., 2021).Fortunately, for both these crops there is a huge amount of genetic variability in wild accessions and commercial cultivars in germplasm banks that can be explored using next-generation sequencing approaches (Piergiovanni, 2022).Therefore, understanding the molecular basis that contributes to the increased or reduced plant branching of these two crops is an important advance for developing these new cultivars with an architecture more suitable to mechanized harvesting (Sandhu and Singh, 2007;Koul et al., 2022;Beveridge et al., 2023).The identification of genes regulating branching architecture in both lentil and chickpea will allow to deliver of candidate targets for biotechnological breeding approaches such as new genome editing technologies and genetic engineering techniques (Basso et al., 2019(Basso et al., , 2020)).Although knowledge of the genetic basis associated with different agronomically important traits of these two crops has been explored in recent years, little is known about the molecular mechanisms involved in the branching and architecture of chickpea and lentil.A recent study identified and characterized the expression profile of SMAX/SMXL family genes in the chickpea and lentil revealing several strigolactonesassociated genes with positive or negative correlations with the plant branching level (Basso et al., 2024a).
Herein, the global transcript expression profile in axillary and apical buds of contrasting cultivars of chickpea and lentil in terms of branching patterns (little and highly branched) was explored by RNA-seq.These collective data revealed several genes putatively associated with the regulation of branching in both chickpea and lentil.These genes are highlighted and discussed as targets for genetic manipulation through genome editing and transgenesis aiming to improve the plant architecture of chickpea and lentil.

Plant material
In this study, two contrasting cultivars of chickpea and lentil were selected dealing with plant branching, according to a previous study carried out by Basso et al. (2024a).The chickpea cultivars Blanco lechoso and FLIP07-318C were used as little and highly branched, respectively.Likewise, lentil cultivars Castellana and Campisi were also used as little and highly branched, respectively.Seeds of the chickpea and lentil cultivars were superficially sterilized with 1.5% sodium hypochlorite solution for 1 minute, washed abundantly with distilled water, soaked for 3 minutes in distilled water, and germinated in Petri plate containing humid filter paper during three days at room temperature.The germinated seeds with a 1-2 cm radicle were transferred to pots containing commercial substrate and kept well-watered and fertilized under greenhouse conditions.

Experimental design
For this study, the chickpea cultivars Blanco lechoso (little branched) and FLIP07-318C (highly branched), and lentil cultivars Castellana (little branched) and Campisi (highly branched) were selected based on a previous study where the architecture/branching of these four cultivars was characterized and, among several cultivars, these four were considered most contrasting for this phenotype (Basso et al., 2024a).The cultivars Blanco lechoso and Castellana are characterized by presenting a low number of lateral branches and a dominant, well-defined, and semierect stem (Scarrone-type plant architecture; Halléand Oldeman, 1970).In contrast, the cultivars FLIP07-318C and Campisi are characterized by presenting a high number of lateral branches and the absence of a dominant, well-defined, and erect stem (Schoutetype plant architecture; Halléand Oldeman, 1970).Axillary buds are the precursor of the branches and lateral shoots, while the apical buds regulate the apical dominance.For this reason, we analyzed both axillary and apical buds for each of the four genotypes.Physiological, hormonal, and transcriptional balance are considered the main factors that define the prevalence of axillary bud or apical bud growth in a given cultivar (Beveridge et al., 2023).This study focused on the identification of genes involved in plant branching using a transcriptomic approach.For this, plant material of chickpea and lentil contrasting cultivars, highly integrity RNA, libraries preparation, high-throughput cDNA sequencing, and RNA-seq raw data were successfully conducted and achieved.

Construction and sequencing of RNA libraries
Axillary and apical buds were collected separately from at least 15 plants randomized per biological replicate after 20 days of transplanting and the samples were kept in liquid nitrogen.Frozen tissues (50-100 mg) were ground to a fine powder with a mortar and pestle using liquid nitrogen.The total RNA was purified with GenUP ™ Total RNA Kit (Biotechrabbit, Volmerstraße, Berlin, Germany).The RNA integrity was checked through agarose electrophoresis, while the concentration of total RNA was measured using a Qubit 4 Fluorometer and Qubit kit (Invitrogen, Waltham, Massachusetts, USA).The purity and integrity of RNA were confirmed by the Agilent Bioanalyser 2100 system (RNA 6000 Nano Kit, Agilent Technologies, Santa Clara, CA, USA).Twentyfour sequencing libraries were prepared using Truseq Stranded mRNA Library Prep and Truseq RNA Single Indexes (Illumina, San Diego, CA, USA) following the manufacturer's instructions.A unique dual index combination was used for each sample/library for barcoding.The concentration of each of the 24 libraries was determined using the Qubit 4 Fluorometer and the dsDNA High Sensitivity Kit (Invitrogen).All samples were sequenced using a NovaSeq 6000 platform (Illumina) and the Novaseq 6000 S1 Reagent Kit (2 x 100 + 10 + 10 bp parameters) following Illumina standard procedure in XP mode.All libraries were run in a single lane of the flow cell.

RNA-seq data elaboration, and differential expression analyses
The RNA-seq raw data in.fastqformat were obtained from BCL files using bcl2fastq2 v2.20 tool (Illumina).The quality assessment of the sequenced libraries was performed with FastQC v0.11.9 (Andrews, 2010).Adaptors and low-quality bases were removed using Trimmomatic PE v0.39 (Bolger et al., 2014).Filtered reads were aligned to the chickpea and lentil genome assemblies using the HiSat2 v2.2.1 tool (Kim et al., 2019).The reference genome used for chickpea data was the C. arietinum CDC Frontier genome ASM33114 assembly v1 (Varshney et al., 2013) while, for lentil data, the CDC Redberry genome v2.0 (Ramsay et al., 2021) was used.Read count was performed using the FeatureCounts v2.0.3 tool with default parameters (Liao et al., 2013) based on the reference transcripts predictions.Differential expression analyses were carried out using the Bioconductor EdgeR package v3.28.1 (Robinson et al., 2009).EdgeR was used to filter out unexpressed or poorly expressed transcripts, normalize the RNA libraries, and perform the differential expression analyses with the Likelihood-Ratio Test (LTR).A transcript was considered 'active' if the reads per million mapping to that transcript were >1 in at least two libraries.Transcripts with a false discovery rate (FDR) <0.05 and log (fold change) [the acronym of log2(fold change)] lower than -2 or greater than +2 were considered to be differentially expressed.

Functional data mining and enrichment analyses
According to the differential expression analyses results, transcripts with the same expression trend (up-or downregulation) were detected for the four pairwise comparisons: chickpea (i) Blanco lechoso axillary bud versus Blanco lechoso apical bud (BX x BA), (ii) FLIP07-318C axillary bud versus FLIP07-318C apical bud (FX x FA), (iii) FLIP07-318C axillary bud versus Blanco lechoso axillary bud (FX x BX), (iv) FLIP07-318C apical bud versus Blanco lechoso apical bud (FA x BA), lentil (v) Campisi axillary bud versus Campisi apical bud (CmX x CmA), (vi) Castellana axillary bud versus Castellana apical bud (CsX x CsA), (vii) Castellana axillary bud versus Campisi axillary bud (CsX x CmX), and (viii) Castellana apical bud versus Campisi apical bud (CsA x CmA).For each differentially expressed transcript in chickpea and lentil their corresponding orthologous genes were identified in Arabidopsis thaliana using BlastX against TAIR10 proteome with an e-value threshold of 10 -5 .The MapMan 3.6.0RC1software was used with the available A. thaliana mapping file (https://mapman.gabipd.org/mapman) to identify and visualize genes in functional overviews of cell pathways and gene categories (Thimm et al., 2004).The transcript set enrichment analysis was carried out with the same list of differentially expressed transcripts using PageMan software (https://mapman.gabipd.org/pageman) (Usadel et al., 2006).The PageMan analysis was performed using the Wilcoxon test without correction and with a cutoff value = 1 (Wilcoxon, 1945).The DAVID database v.6.8 (Dennis et al., 2003) was used to obtain the gene ontology (GO) information related to each biological process.KEGG pathway enrichment analyses were carried out on differentially expressed transcript sets to identify relevant pathways enriched for each pairwise comparison.The KEGG pathway enrichment analyses were conducted with KOBAS-i web tool (Bu et al., 2021).While chickpea is a species supported by KOBAS-i, lentil is not, so DETs Arabidopsis orthologs were used for lentil's enrichment analyses.The bubble diagrams were plotted with ggplot2 v3.4.3 R visualization package (Wickham, 2016).The chromosomal location of the chickpea and lentil genes was evidenced by the MapGene2Chrom program v2 (Jiangtao et al., 2015).

Gene expression profile by real-time RT-PCR
The RNA samples purified as described above were treated with RNase-free RQ1 DNase I (Promega, Madison, Wisconsin, EUA) and used for cDNA synthesis using oligo-(dT) 20 primer and SuperScript III RT mix (Life Technologies, Carlsbad, CA, USA).The cDNA samples were diluted 1:10 (v:v) with nuclease-free water, while the real-time RT-PCR assays were performed in QuantStudio 7 Flex Real-Time PCR platform (Applied Biosystems, Waltham, MA, USA) using 2.5 µL cDNA, 0.1 µM gene-specific primers (Supplementary Table S1), and SYBR Green PCR Master Mix (Applied Biosystems, Waltham, MA, USA).For validation of RNA-seq data, the CaBES1, CaFHY3, CaFAR1, CaDOF4.2, and CaFHY1 genes were selected for evaluation in chickpea samples, while LcFITNESS, LcFHY3, LcFAR1, LcDOF4.2, and LcBS1 genes were selected for lentil samples (Supplementary Tables S1, S2).The CaCAC (Reddy et al., 2016) and LcTUB (Sinha et al., 2019) were used as endogenous reference genes for normalization (Supplementary Table S1).The reference genes CaG6PD and CaTIP41, LcRPL2, and LcRBC1 were also tested, but CaCAC and LcTUB were more stable in our preliminary test as a reduced number of samples.The relative gene expression, fold change, and log(fold change) were calculated with the 2^-DCt, 2^-DDCt, and Log(fold change) formulas, respectively.Three biological replicates for each treatment and at least 15 plants for each biological replicate were used.All cDNA samples were carried out in technical triplicates.The target-specific amplification for each pair primer was confirmed by the occurrence of a single peak observed in the melting curve.To validate the transcriptional level obtained from RNA-seq datasets, the relative or normalized expression values (2^-DCt) obtained from real-time RT-PCR were correlated using the Pearson correlation coefficient to normalized expression values based on transcript per million (TPM) values obtained from RNA-seq for each of the five selected genes in each library or sample, for both chickpea and lentil.

RNA-seq libraries construction, data elaboration, and differential expression analysis
In total, 24 libraries were constructed and sequenced, 12 libraries for chickpea and 12 for lentil (two cultivars each x two tissues x three biological replicates).One library of the cultivar FLIP07-318C corresponding to the axillary bud sample was removed from subsequent bioinformatic analyses due to the reduced number of reads.The raw sequences of the RNA libraries were deposited on the EMBL-EBI ArrayExpress database (https:// www.ebi.ac.uk/biostudies/arrayexpress) under the accession number E-MTAB-13679.Overall, taking together the RNA-seq raw reads generated from the 11 chickpea libraries, 90.79 to 93.59% of these paired reads passed quality control and filtering steps.In total, 3,091.832 to 13,316.821filtered reads were obtained, of which 97.39 to 98.57% were mapped to the transcript dataset of the reference genome (Supplementary Table S2).In contrast, from RNA-seq raw reads generated from the 12 lentil libraries, 90.76 to 94.02% of these paired reads passed quality control and filtering steps, 5,862.483 to 12,410.646filtered reads were obtained, of which 93.68 to 96.56% were mapped to the transcript dataset of the reference genome (Supplementary Table S2).The number of reads per library mapped to each of the chickpea and lentil reference transcripts was estimated and, among them, only 14,324 and 20,884, respectively, resulted as active transcripts, and were used for further analyses (Supplementary Files S1, S2).The 23 RNA libraries were normalized according to the amounts of filtered reads.Then, filtered and normalized counts were plotted in a multidimensional scaling (MDS) graph.The PCA graphs showed groups partially separated by cultivar and tissue evaluated both for chickpea (Figure 1A) and lentil (Figure 1B).
A total of 1,624 and 2,512 differentially expressed transcripts were identified after our cutoff between pairwise comparisons of chickpea (BX vs BA, FX vs FA, FX vs BX, and FA vs BA) and lentil (CmX vs CmA, CsX vs CsA, CsX vs CmX, and CsA vs CmA), respectively (Supplementary Files S1, S2).Among differentially expressed chickpea transcripts, a total of 94 (BX vs BA), 1,147 (FX vs FA), 974 (FX vs BX), and 282 (FA vs BA) were considered up-or down-regulated (Figure 1C).In contrast, in lentil, a total of 49 (CmX vs CmA), 829 (CsX vs CsA), 1,375 (CsX vs CmX), and 1,905 (CsA vs CmA) were considered up or down-regulated (Figure 1D).Taking together the eight pairwise comparisons in chickpea, the number of up-regulated transcripts ranged from 88 to 1,043 while the down-regulated transcripts ranged from 6 to 240 (Figures 1C, E, F).Meanwhile, in the pairwise comparisons of the eight lentil treatments, the number of up-regulated transcripts ranged from 13 to 1,226, while the down-regulated transcripts ranged from 36 to 681 (Figures 1D, G, H).Therefore, several transcripts were identified as differentially expressed in pairwise comparison between different tissues and contrasting cultivars.

Differentially expressed transcript set enrichment analyses reveal the modulated biological processes
The enrichment analysis of differentially expressed transcript set from chickpea showed that jasmonic acid (JA) metabolism, cell division, DNA replication, cell cycle, RNA biosynthesis (MADS/ AGL-type transcription factor), cell wall organization, and plant reproduction were significantly down-regulated, while RNA biosynthesis (C2H2 transcription factor), solute transport, and nutrient uptake were significantly up-regulated in axillary buds of cultivar Blanco lechoso (little branched) compared with the cultivar FLIP07-318C (highly branched) (Figure 2).In contrast, RNA biosynthesis and external stimuli response (UV-A/blue light) were significantly down-regulated, while protein homeostasis and protein quality control were significantly up-regulated in apical buds of cultivar Blanco lechoso (little branched) compared with the cultivar FLIP07-318C (highly branched) (Figure 2).Moreover, the enriched categories with differentially expressed transcripts between axillary and apical buds of the chickpea cultivar Blanco lechoso were not differentially modulated, while chromatin organization, cell division, DNA replication, cell division, cell cycle, DNA damage response, protein biosynthesis, protein phosphorylation, cell wall organization, acyltransferases (EC 2.3), and ligases (EC 6.5) were significantly down-regulated, while carbohydrate metabolism, amino acid metabolism, phytohormone action, RNA biosynthesis, external stimuli response (UV-A/blue light), and glycosyltransferases (EC 2.4), and ligases (EC 6.3) were up-regulated in apical buds of the chickpea cultivar FLIP07-318C compared with the axillary buds of the same cultivar (Figure 2).
Similarly, the enrichment analysis of differentially expressed transcript set from lentil showed that protein biosynthesis (pre-40S ribosomal subunit) was down-regulated, while lipid metabolism, nucleotide metabolism, chromatin organization, RNA processing, protein biosynthesis and homeostasis (quality control and ubiquitin-proteasome system), cell wall organization, solute transport, oxidoreductases (EC 1.10), and isomerases (EC 5) were up-regulated in axillary buds of cultivar Campisi (highly branched) compared with the cultivar Castellana (little branched) (Figure 3).In contrast, RNA biosynthesis and protein biosynthesis (pre-40S ribosomal subunit) were significantly down-regulated, while photosynthesis, amino acid metabolism, nucleotide metabolism, chromatin organization, cell division and cycle, RNA processing, protein biosynthesis, protein homeostasis, solute transport, oxidoreductases (EC 1.10), and isomerases (EC 5 and EC 5.4) were up-regulated in apical buds of cultivar Campisi (highly branched) compared with the cultivar Castellana (little branched) (Figure 3).In addition, the enriched categories with differentially expressed transcripts between axillary and apical buds of the lentil cultivar Castellana showed that carbohydrate metabolism, amino acid metabolism, nucleotide metabolism (pyrimidines), phytohormone action, RNA biosynthesis, protein homeostasis, proteolysis, programmed cell death, oxidoreductases (EC 1.3 and EC 1.14), and ligases (EC 6.3) were significantly down-regulated, while chromatin organization, cell division, DNA replication, cell division, cell cycle, RNA processing (silencing), cytoskeleton organization, solute transport (MATE family), and plant reproduction were up-regulated in apical buds of cultivar Castellana (little branched) compared with the axillary buds of the same cultivar (Figure 3).Meanwhile, the enriched categories with differentially expressed transcripts between axillary and apical buds of the lentil cultivar Campisi were not differentially modulated (Figure 3).Therefore, several biological processes were modulated in pairwise comparison between different tissues and contrasting cultivars of chickpea and lentil, highlighting hormonal pathways, cell cycle, RNA and protein synthesis, and plant development and reproduction.

GO and KEGG pathway enrichment analyses reveal the functional profile of differentially expressed transcripts
The GO enrichment analyses were carried out with differentially expressed transcripts to evidence the biological mechanisms associated with little or highly branched.The GO enrichment analysis of differentially expressed transcript set from chickpea showed that several clusters were arranged to represent the categories associated with the photosystem, cytochrome P450, transmembrane, transport, stress protein, and secondary metabolism from up-regulated transcripts, while the categories associated with the cell division, cell cycle, cell organization, transferases, secondary metabolism, oxidoreductases, and DNA transcription were represented from down-regulated transcripts in axillary buds of cultivar Blanco lechoso (little branched) compared with the cultivar FLIP07-318C (highly branched) (Supplementary File S3).In contrast, the categories associated with the response to heat stress, chaperone, DnaJ transcription Transcript set enrichment categories for the two pairwise comparisons using the PageMan web tool.The green and red extremes represent the metabolic pathways differentially modulated between contrasting cultivars and tissues of chickpea.Only differentially expressed transcripts with FDR <0.05 and log(fold change) lower than -2 or greater than +2 were considered in the pathway analysis.The color intensity is correlated with the statistical significance based on the Wilcoxon test default implemented in the PageMan tool.
factors, and cell wall were up-regulated, while the categories associated with sugar metabolism, DNA transcription, oxidoreductase, metal binding, and RNA binding were downregulated in apical buds of cultivar Blanco lechoso compared with the cultivar FLIP07-318C (Supplementary File S3).In addition, the categories associated with DNA transcription, oxidoreductase, dioxygenase, and peptidase were up-regulated, while no category was down-regulated in apical buds of cultivar Blanco lechoso compared with axillary buds of the same cultivar (Supplementary File S3).Meanwhile, the categories associated with transmembrane, oxidoreductase, dioxygenase, metal binding, cytochrome P450, gibberellin biosynthesis, amino acid transport, nitrate assimilation, sugar metabolism, DNA binding, kinases, and secondary metabolism were up-regulated, while the categories associated with genome integrity, histone, lipid metabolism, DNA methylation, DNA binding, and metal binding were downregulated in apical buds of cultivar FLIP07-318C compared with axillary buds of the same cultivar (Supplementary File S3).Similarly, the GO enrichment analysis of differentially expressed transcript set from lentil showed that several categories associated with the transmembrane transport, lipid metabolism, cytoskeleton organization, metal binding, cytochrome P450, sugar metabolism, response to endoplasmic reticulum stress, and proteolysis were up-regulated, while the categories associated with ATP-binding, kinases, signaling, transport, DNA binding, and ubiquitin were down-regulated in axillary buds of cultivar Campsi (highly branched) compared with the cultivar Castellana (little branched) (Supplementary File S3).In addition, the categories associated with lipid metabolism, transmembrane transport, peptidase, metal binding, cell cycle, and cytoskeleton organization were up-regulated, while the categories associated with ATPbinding, sugar metabolism, lipid metabolism, glucosyltransferase, kinase, chaperone, metal binding, DNA binding, signaling, and chloroplast stroma were down-regulated in apical buds of cultivar Campsi compared with the cultivar Castellana (Supplementary File S3).Meanwhile, the categories associated with the DNA-binding, cell cycle, genome integrity, ATP-binding, and zinc finger were upregulated transcripts, while the categories associated with sugar metabolism, oxidoreductase, cytochrome P450, metal binding, DNA-binding, signaling, kinases, hormone biosynthesis, secondary metabolism, and transmembrane were down-regulated in apical buds of cultivar Castellana compared with axillary buds of the same cultivar (Supplementary File S3).In the same sense, no GO category was up-regulated, while the categories associated with metabolic pathways and kinase activity were down-regulated in apical buds of cultivar Campisi compared with axillary buds of the same cultivar (Supplementary File S3).Therefore, the differentially expressed transcripts in chickpea modulated for greater energy production and lower cell cycle in axillary buds while greater metabolism and lower development in apical buds of the highly branched cultivar.Meanwhile, in lentil these transcripts modulated for lower metabolism and proteolysis and greater signaling in axillary buds while lower cell cycle and higher metabolism in apical buds of the highly branched cultivar.Similarly, KEGG pathway enrichment analyses on differentially expressed transcripts among pairwise comparisons of genotypes and tissues showed significant enrichments for pathways as metabolic processes, biosynthesis of secondary metabolites, and signal transduction for both chickpea (Supplementary Figures S2A-D) and lentil (Supplementary Figures S3A-D).

Sucrose-triggered signaling pathway
Representative sets of differentially expressed transcripts were identified as interconnected in the sucrose-triggered signaling pathway in the comparison between apical and axillary buds and contrasting cultivars of chickpea and lentil (Table 1).From the chickpea datasets, 19 main transcripts involved in carbohydrate transport, inositol transport, raffinose biosynthesis, sucrose biosynthesis, dihydroxyacetone phosphate biosynthesis, carbohydrate efflux, sugar sensing, sucrose transport, and sugar signaling were identified as differentially expressed (Table 1).The main changes observed in chickpea were the up-regulation of all these genes, except for the down-regulation of CaGPT2 and CaSWEET3 genes, in axillary buds compared to apical buds of cultivar FLIP07-318C (highly branched).Meanwhile, the CaSUS3 and CaSnRK1/KING1 genes were up-regulated in the axillary buds compared with apical buds of cultivar Blanco lechoso (little branched).Similarly, all 19 genes were also considered upregulated in the axillary buds of cultivar FLIP07-318C (highly branched) compared to the axillary buds of cultivar Blanco lechoso (little branched), except for the down-regulation of the CaSWEET3 gene.Also, the CaGPT2, CaSWEET4, and CaSIP2 genes were considered up-regulated while CaSIP1 and CaFBP1 were down-regulated in the apical buds of cultivar FLIP07-318C compared to cultivar Blanco lechoso (little branched).Therefore, these chickpea data suggest that metabolism and sucrose-mediated signaling are more active in axillary buds of the highly branched cultivar compared with apical buds of the same cultivar and axillary buds of the little branched cultivar.
Likewise, from the lentil datasets, 15 main transcripts involved in dihydroxyacetone phosphate biosynthesis, inositol transport, carbohydrate transport, sugar sensing, sucrose degradation, UDPsugar transport, sugar signaling, and sucrose transport were identified as differentially expressed (Table 1).The main changes observed in lentil were the down-regulation of almost all these genes in axillary buds compared to apical buds of cultivar Castellana (little branched).Meanwhile, the LcSuSy1, LcSuSy2, and LcUST1 genes were down-regulated in the axillary buds of cultivar Castellana (little branched) compared with Campisi (highly branched) (Table 1).Similarly, the up-regulation of almost all these genes in apical buds of cultivar Castellana compared to cultivar Campisi was observed, except for the down-regulation of LcSuSy1, LcSuSy2, LcUST1, and LcSUC1 genes.In particular, the expression of this gene set showed no changes in the expression profile between axillary and apical buds of highly branched cultivar.These lentil data suggest that metabolism and sucrose-mediated signaling are more active in the apical buds of little branched cultivar compared to highly branched cultivar, while this process is balanced between apical and axillary buds of highly branched cultivar.Therefore, the metabolism and sucrose-mediated signaling pathway have a strong positive correlation in the increased branching or apical dominance in both chickpea and lentil.

Trehalose-6-phosphate-triggered signaling pathway
Several trehalose-6-phosphate synthase (TPS) transcripts were differentially expressed in the comparison between apical and axillary buds and contrasting cultivars of chickpea and lentil (Table 2).In particular, four CaTPS genes were up-regulated in apical buds of cultivar FLIP07-318C (highly branched) compared with axillary buds of the same cultivar, while three of these genes were down-regulated in apical buds of cultivar Blanco lechoso (little branched) compared with apical buds of cultivar FLIP07-318C.Likewise, four LcTPS genes were down-regulated in apical buds of cultivar Castellana (little branched) compared with axillary buds of the same cultivar, while these same genes were up-regulated in apical buds of cultivar Campisi (highly branched) compared with the cultivar Castellana.Meanwhile, two trehalose-6-phosphate phosphatase (TPP) genes were also up-and down-regulated when compared axillary and apical buds of cultivar FLIP07-318C, and up-regulated in these tissues when compared both cultivars (Table 2).Likewise, three LcTPP genes were down-regulated, mainly in apical and axillary buds of cultivar Campisi compared with the cultivar Castellana.For instance, both hexokinase-1 (HXK1) genes were down-regulated in apical buds of cultivar FLIP07-318C compared with axillary buds of the same cultivar, and in axillary buds of cultivar Blanco lechoso compared with the cultivar FLIP07-318C (Table 2).Meanwhile, only the LcHXK1.2gene was up-regulated in apical buds of cultivar Castellana compared with axillary buds of the same cultivar.Likewise, the CaSnRK1/KIN10 and CaSnRK1/KIN11 genes were respectively down-regulated in axillary buds of cultivar Blanco lechoso compared with the cultivar FLIP07-318C, and up-regulated in apical buds of cultivar FLIP07-318C compared with axillary buds of the same cultivar (Table 2).Likewise, LcSnRK1/KIN11 gene was down-regulated in apical buds of cultivar Castellana compared with the axillary buds of the same cultivar, while was up-regulated in apical buds of cultivar Campisi compared with the cultivar Castellana.Lastly, the sugar transporter protein 1 (STP1) gene, which is not directly related to the trehalose-6-phosphate pathway, but contributes to the regulation of genes involved in shoot branching through carbon partitioning, was up-regulated in apical buds of cultivar FLIP07-318C compared with axillary buds of the same cultivar, and also up-regulated in axillary buds of cultivar Blanco lechoso compared with the cultivar FLIP07-318C (Table 2).Meanwhile, the LcSTP1 gene was down-regulated in apical buds of cultivar Castellana compared with axillary buds of the same cultivar, and up-regulated in apical buds of cultivar Campisi compared with the cultivar Castellana.Therefore, these collective data showed that the trehalose-6-phosphate biosynthesis and signaling pathway and TPS1-mediated signaling were differentially modulated between different tissues and contrasting cultivars of both chickpea and lentil.

Different hormonal signaling pathways
Additional enrichment analyses were focused on hormonal pathways modulated in the comparison of the same tissue between little and highly branched genotypes.The comparison of axillary buds of cultivar Blanco lechoso (little branched) with the cultivar FLIP07-318C (highly branched) showed that several upregulated transcripts were involved in abscisic acid (ABA) biosynthesis and auxin, ethylene, cytokinin and brassinosteroid, strigolactone biosynthesis and signal transduction, while downregulated categories were involved in auxin conjugation and degradation, ethylene biosynthesis, gibberellin biosynthesis, and JA biosynthesis, conjugation and degradation (Supplementary File S4).In addition, the up-regulated transcripts involved in auxin biosynthesis, JA biosynthesis, and strigolactones biosynthesis, while the down-regulated transcripts involved in auxin conjugation and degradation, cytokinin biosynthesis and signal transduction, gibberellin biosynthesis, and JA biosynthesis were represented in apical buds of cultivar Blanco lechoso contrasted with the cultivar FLIP07-318C (Supplementary File S4).Meanwhile, up-regulated transcripts involved in ABA biosynthesis, auxin conjugation and degradation, ethylene biosynthesis, JA biosynthesis, conjugation and degradation were represented in apical buds of cultivar Blanco lechoso contrasted with axillary buds of the same cultivar, while the down-regulated transcripts did not impact hormonal pathways (Supplementary File S4).In the same sense, upregulated transcripts involved in ABA biosynthesis, signaling and degradation, auxin signaling and degradation, cytokinin biosynthesis and signaling, ethylene biosynthesis, gibberellin biosynthesis, signal transduction and degradation, and JA biosynthesis and degradation, while down-regulated transcripts involved in cytokinin signaling were represented in the apical buds of cultivar FLIP07-318C contrasted with axillary buds of the same cultivar (Supplementary File S4).
Similarly, the differentially expressed transcript set from lentil showed that several up-regulated transcripts involved in auxin signaling, cytokinin degradation, and JA biosynthesis, while the down-regulated transcripts involved in ABA signaling and degradation, and auxin degradation were represented in the axillary buds of cultivar Campisi (highly branched) contrasted with the cultivar Castellana (little branched) (Supplementary File S4).In addition, up-regulated transcripts involved in ABA biosynthesis and transport, auxin signaling, auxin signaling, brassinosteroid biosynthesis and signaling, cytokinin biosynthesis and degradation, ethylene biosynthesis and signaling, gibberellin biosynthesis, signaling and degradation, and JA biosynthesis, signaling and degradation were represented in the apical buds of cultivar Campisi contrasted with the cultivar Castellana (Supplementary File S4).Meanwhile, the up-regulated transcripts involved in JA degradation, and down-regulated transcripts involved in ABA biosynthesis, signaling and degradation, auxin transport, brassinosteroid signaling, cytokinin biosynthesis, ethylene biosynthesis and signaling, gibberellin biosynthesis, signaling and degradation, JA biosynthesis, and strigolactones signaling were represented in the apical buds of cultivar Castellana contrasted with axillary buds of the same cultivar (Supplementary File S4).In the same sense, the down-regulated transcripts involved in JA biosynthesis were represented in the apical buds of cultivar Campisi contrasted with axillary buds of the same cultivar, while the up-regulated transcripts did not impact hormonal pathways (Supplementary File S4).Therefore, the differentially expressed transcripts in chickpea modulated the ABA, auxin, brassinosteroid, cytokinin, ethylene, gibberellin, JA, and strigolactones in axillary buds while auxin, JA, and strigolactones in apical buds of the highly branched cultivar compared with little branched cultivar.Meanwhile, in lentil these transcripts modulated auxin, cytokinin, JA, and ABA in axillary buds while ABA, auxin, brassinosteroid, cytokinin, ethylene, gibberellin, and JA in apical buds of the highly branched cultivar compared with little branched cultivar.

Cytokinin and auxin signaling pathways
Several transcripts enriched for cytokinin and auxin pathways were found to be differentially expressed in contrasting chickpea and lentil cultivars (Supplementary File S4; Table 3).In the chickpea dataset, the 10 main genes involved in the cytokinin pathway are annotated as involved in cytokinin degradation, transmembrane receptor, biosynthesis, signaling, and transport, while the five main genes associated with the auxin pathway are annotated as involved in auxin signaling, biosynthesis, transport, and degradation (Table 3).All of these genes were up-regulated in axillary buds compared to apical buds of the FLIP07-318C cultivar (highly branched), except for the down-regulation of CaAHP6 gene.In contrast, only CaILR1 gene was up-regulated in axillary buds compared to apical buds of the Blanco lechoso cultivar (little branched).Meanwhile, nine genes were up-regulated and two genes (CaAHP6 and CaILR1) were down-regulated in axillary buds of the highly branched cultivar compared with the little branched cultivar.Likewise, six genes were down-regulated and two genes (CaAux/IAA14 and CaYUC10) were up-regulated in apical buds of the highly branched cultivar compared with the little branched cultivar.
In the lentil dataset, the four main genes involved in the cytokinin pathway are annotated as involved in cytokinin transmembrane receptor, signaling, biosynthesis, and degradation, while the seven main genes associated with the auxin pathway are annotated as involved in auxin transport, transmembrane receptor, and signaling (Table 3).Four of these genes (LcCYP35A1, LcZOG1, LcPILS1, and LcAux/IAA14) were down-regulated in axillary buds compared to apical buds of the Castellana cultivar (little branched).In contrast, none of these genes were differentially expressed in axillary buds compared to apical buds of the Campisi cultivar (highly branched).Meanwhile, four genes were up-regulated and another four genes were down-regulated in the axillary buds of the little branched cultivar compared with the highly branched cultivar.Likewise, four genes were down-regulated and another seven genes were up-regulated in apical buds of the little branched cultivar compared with the highly branched cultivar.Therefore, since it is well known that the cytokinin and auxin pathways act on each other, providing regulatory feedback to control apical dominance and plant branching, the differential expression profile of several genes involved in different functions suggests that these two hormonal pathways play a remarkable role in modulating the branching of contrasting chickpea and lentil cultivars.

Strigolactones signaling pathway
The CCD subfamily genes (Basso et al., 2023) and SMAX/SMXL family genes (Basso et al., 2024a) of chickpea and lentil, both involved in carotenoids and dependent and independent strigolactones and karrikins pathways, were also exploited to evidence the strigolactones signaling modulation and eventual association with the branching phenotype.In particular, the CCD subfamily contains genes involved in the degradation of carotenoids for the production of strigolactones and other volatile and nonvolatile compounds, while chickpea and lentil SMAX1/SMXL1 genes are involved in the strigolactones and karrikins-dependent signaling pathway for regulation of shoot branching and hairy root elongation (Basso et al., 2023;Basso et al., 2024a).Meanwhile, the chickpea and lentil SMXL6 to SMXL8 genes are involved in the strigolactones-dependent signaling pathway for the regulation of shoot branching and elongation, and the chickpea and lentil SMXL2 and SMXL3 genes are involved in the strigolactones-and karrikinsindependent signaling pathway for the regulation of phloem formation (Basso et al., 2024a).In this study, the CaCCD2, CaSMAX1/SMXL1, CaSMXL2, and CaSMXL7 genes were upregulated while the CaSMXL5 gene was down-regulated in the apical buds of cultivar FLIP07-318C (highly branched) and axillary buds of cultivar Blanco lechoso (little branched) contrasted with axillary buds of the cultivar FLIP07-318C (Table 4).Meanwhile, the LcCCD1, LcCCD5, LcSMAX1/SMXL1, LcSMXL6, LcSMXL7, and LcBRC1 genes were down-regulated in the apical buds of cultivar Castellana (little branched) compared with axillary buds of the same cultivar (Table 4).In addition, the LcCCD1, LcCCD5, LcSMXL3, and LcSMXL7 genes were up-regulated in the apical buds of cultivar Campisi (highly branched) contrasted with the cultivar Castellana (Table 4).Therefore, the strigolactones biosynthesis and signaling pathway is differentially modulated between different tissues and contrasting cultivars of both chickpea and lentil and this differential modulation is marginally associated with the different branching profiles of the plants.

Branching-related transcription factors
Several transcription factors with notable involvement in the regulation of plant branching were particularly monitored in the

RNA-seq validation by real-time RT-PCR
In order to validate the RNA-seq expression data, five genes of chickpea and five genes of lentil were randomly selected to evaluate the expression profile via real-time RT-PCR in the same tissues and contrasting cultivars.The RNA-seq results were successfully validated by real-time RT-PCR for the five selected genes both in chickpea and lentil.The Pearson correlation coefficient alongside the p-values showed that genes had a significant positive correlation supported by p-value ≤0.05 (Supplementary Table S3), indicating that these genes exhibited equivalent expression patterns between RNA-seq and real-time RT-PCR datasets.The chickpea CaBES1 (branching-related; Hu et al., 2020), CaFHY1, CaFHY3 and CaFAR1 (branching-related; Stirnberg et al., 2012;Xie et al., 2020), and CaDOF4.2(branching-related; Zou et al., 2012) genes were monitored and revealed accordance for differential expression level between RNA-seq versus real-time RT-PCR of 90%   S3; Supplementary Figures S5, S6).Therefore, transcript expression data via RNA-seq are supported with high agreement by real-time RT-PCR data.

Discussion
There is currently a considerable number of chickpea and lentil accessions, genotypes, and cultivars in germplasm banks around the world with enormous genetic and phenotypic variability mainly related to plant architecture (Piergiovanni, 2022).In particular, chickpea and lentil plants with low branching, erect growing stems, high apical dominance, high pod productivity, and high grain yield per plant are desired agronomic characteristics in commercial cultivars (Asati et al., 2022;Mitache et al., 2024).Therefore, significant efforts are still needed in plant breeding and genetic engineering to develop superior cultivars of chickpea and lentil better adapted to mechanized planting and harvesting systems (Singh et al., 2019;Yang et al., 2021).Furthermore, improving plant architecture can impact the grain productivity versus biomass ratio, reduce susceptibility to abiotic and biotic stresses, and increase production and yield per cultivated area (Basso et al., 2024a).In this way, expanding knowledge about the genetic basis associated with the regulation of plant branching can provide biotechnological assets and contribute to the improvement of these crops.In this present study, the global transcript expression profile was evaluated in two contrasting cultivars and two main tissues associated with the modulation of branching in chickpea and lentil plants.For this, the chickpea cultivars Blanco lechoso and FLIP07-318C and the lentil cultivars Castellana and Campisi were previously determined as phenotypically contrasting with each other in terms of branching profile (Basso et al., 2024a).In this sense, the axillary and apical buds were chosen for evaluation, since they are the major tissues involved in the plant branching.In addition, it is important to mention that the fine-tuning between apical and axillary activity are determining factors to regulate cotyledonary branching or apical dominance (Beveridge et al., 2023).This balance is orchestrated by numerous factors, mainly gene expression and hormones, and is led by the signaling coming from the primary shoot apex (Kebrom, 2017;Yuan et al., 2023).For example, if the main apex is removed or its activity reduced, dormant axillary buds below can be activated (Ongaro et al., 2008;Müller & Leyser, 2011).Our RNA-seq study revealed a total of 1,624 and 2,512 differentially expressed transcripts in chickpea and lentil datasets, respectively.Objectively, part of them can be categorized into mechanisms closely associated with the modulation of branching, while the other part is involved secondarily or indirectly in plant branching.Furthermore, it must be considered that many mechanisms are interconnected and act on each other to provide regulatory feedback (Barbier et al., 2019;Salam et al., 2021).In view of this, herein were desiccated the influence of differentially expressed transcripts on the major pathways closely associated with the regulation of chickpea and lentil branching, such as sucrose-and trehalose-6-phosphatetriggered signaling pathways, hormonal balance, auxin, cytokinin and strigolactones signaling pathways, and major transcriptions factors and genes linked to multiple mechanisms.Therefore, the dissection of these major pathways, transcription factors, and genes can provide consolidated data to improve understanding of the mechanisms involved in the branching control of chickpea and lentil and can reveal suitable target genes to be evaluated for the biotechnological potential through transgenesis and genome editing.

Sucrose-triggered signaling pathway
The proper functioning of essential biological processes are determining factors for plant growth, branching, flowering, and seed production (Julius et al., 2017;Wingler and Henriques, 2022).The tuning of these processes and transitioning to the next phase is finely adjusted and modulated by the influence of good or   stressful conditions to which the plants are exposed (Lemoine et al., 2013;Beveridge et al., 2023).In particular, similar to increased auxin concentration in the apical buds, the availability and supply of sugars to meet the demand of the apical meristem and the limitation for axillary buds are some of the main factors that determine apical dominance (Mason et al., 2014).Therefore, the signaling pathway triggered by these sugars such as sucrose, glucose, fructose, and trehalose-6-phosphate contributes to regulating from the developmental stage transitions to plant branching, following source-to-sink flux and linked with hormonal signaling (Wingler, 2017;Barbier et al., 2019;Salam et al., 2021).In particular, sucrose and trehalose-6-phosphate are closely related to plant branching regulation, while glucose and fructose act secondarily on the modulation of plant growth and branching (Figueroa and Lunn, 2016;Barbier et al., 2019).Sucrose is the main sugar since it can be transported by phloem over long distances and may regulate plant branching by directly inducing bud outgrowth, by inhibiting or antagonizing the strigolactones signaling pathway in different steps, or by inducing cytokinin biosynthesis (Lemoine et al., 2013;Salam et al., 2017;Barbier et al., 2019).Overall, the shoot tip growth inhibits axillary bud outgrowth because the shoot tip is a sink for sucrose, depriving axillary buds of sugar (Barbier et al., 2015).Although sucrose acts directly in certain signaling processes, once in the axillary bud or apical meristem, it also leads to trehalose-6-phosphate accumulation and both can inhibit the central growth repressors SnRK1 kinases (Barbier et al., 2019;Fichtner et al., 2021).In this way, both sucrose and trehalose-6-phosphate act on each other to provide feedback under the regulatory pathway (Stein and Granot, 2019).In particular, the sucrose-triggered signaling pathway for branching modulation is mediated mainly by trehalose-6phosphate and secondly by glucose, fructose, and other intermediate sugars (Miyagawa et al., 2001;Barbier et al., 2015;Otori et al., 2017).In our RNA-seq datasets were identified 19 and 15 main differentially expressed transcripts as involved in sucrose metabolism, transport, signaling, and sensing both in chickpea and lentil, respectively.In particular, among the main differentially expressed genes identified as associated with chickpea and lentil branching modulation are SWEETs involved in sugar bidirectional transport (Gautam et al., 2022), EXL2 involved in sugar sensing (Schröder et al., 2012), SnRK1 involved in sugar signaling and bud outgrowth inhibition (Barbier et al., 2019), INTs involved in inositol transport (Strobl et al., 2018), as well as several other genes involved in sucrose biosynthesis or catabolism, such as, for example, SIP2 (Peters et al., 2010) and SuSy (Stein and Granot, 2019).The transgenic overexpression of the CmSWEET17 gene promoted axillary bud growth in Chrysanthemum morifolium by also inducing upregulation of several auxin transporter genes (Liu et al., 2019).
In turn, EXL2 (EXORDIUM-like) genes are associated with bud dormancy and are involved in sugar sensing with a role under carbon starvation conditions (Schröder et al., 2012;Tarancoń et al., 2017).In the meantime, the SnRK1 kinase complex acts as a central repressor of plant growth and bud dormancy, integrating nutrient status at the cellular level and regulating cell growth arrest in nutrient-limiting conditions (Martıń-Fontecha et al., 2018;Barbier et al., 2019).The SnRK1/KING1 gene was identified as differentially modulated with a positive correlation between expression with branching or apical dominance in both chickpea and lentil, which is a major regulator connecting sucrose metabolism with enzyme activities through the SnRK1 targets (Stefan et al., 2022).Likewise, the inositol transporters encoded by INT genes act as H + /myo-inositol symporters across the plasma membrane from the vacuole into the cytoplasm and are closely related to cell elongation, plant growth, and branching (Schneider et al., 2006;Strobl et al., 2018).Therefore, these data support that metabolism and sucrose-mediated signaling pathway are positively correlated with enhanced axillary branching or apical dominance in these crops.Similar results were observed in Arabidopsis and tobacco, indicating that carbon partitioning alterations significantly affect shoot branching development (Freixes et al., 2002;Tamoi et al., 2014;Otori et al., 2017).
Trehalose-6-phosphate-triggered signaling pathway Trehalose is used as a carbon source and protective compound towards adverse conditions, while its phosphorylated intermediate, trehalose-6-phosphate, is a sugar-signaling metabolite that regulates several biological processes including plant branching (Ponnu et al., 2011;Nunes et al., 2013;Paul et al., 2018).The trehalose-6-phosphate promotes plant branching by inhibiting the activity of SnRK1/KIN10 and SnRK1/KIN11 proteins (Zhang et al., 2009;Wingler and Henriques, 2022;Morales-Herrera et al., 2023).In Arabidopsis, TPS enzymes convert glucose-6-phosphate and UDP-glucose into trehalose-6phosphate, while trehalose-6-phosphate is dephosphorylated into trehalose by TPP enzymes, and then hydrolyzed by trehalase (TRE1) enzyme into two glucose molecules (Ponnu et al., 2011;Gazzarrini and Tsai, 2014).For instance, the HXK1 enzyme converts glucose into glucose 6-phosphate, which is used by TPS enzymes to produce trehalose-6-phosphate (Barbier et al., 2021).The TPS gene overexpression in Arabidopsis increased trehalose and trehalose-6-phosphate levels and resulted in a dehydration tolerance phenotype and delayed flowering (Avonce et al., 2004;Fichtner et al., 2020).Likewise, TPP gene overexpression in Arabidopsis improved stress tolerance by accumulating soluble sugar and jasmonic acid and reduced plant branching, while the knockout mutant resulted in drought-sensitive plants (Lin et al., 2019;Fichtner et al., 2021;Lin et al., 2023).In contrast, the overexpression of the TRE1 gene in Arabidopsis improves drought tolerance (Van Houtte et al., 2013).Herein, the trehalose-6-phosphate pathway was emphasized and a parallel was drawn with the contrasting branching profile of chickpea and lentil cultivars.In particular, our transcript expression data showed up-regulation of some TPS genes and suggested a higher trehalose-6-phosphate accumulation in apical buds of highly branched cultivars of chickpea and lentil.However, in apical buds of these cultivars highly branched there was also upregulation of transcripts coding for the SnRK1 protein that inhibits branching, while down-regulation of transcripts coding for the HXK1 proteins that stimulate branching both in chickpea and lentil.The HXK1 acts as a central sugar-sensing and -signaling protein and is involved in stimulating bud outgrowth, increasing plant branching, and promoting juvenile-to-adult phase transition upstream of cytokinin and strigolactone signaling pathways (Wingler, 2017;Barbier et al., 2021).The AtHXK1 gene overexpression resulted in Arabidopsis plants without apical dominance and increased emergence of lateral shoots (Kelly et al., 2012), while knockout mutant plants showed decreased cytokinin levels, increased expression of MAX2 gene, sugar-insensitive phenotype, and reduced growth and branching (Avonce et al., 2004;Barbier et al., 2021;Li et al., 2023).Likewise, the STP1 gene was finely up-regulated in apical buds of cultivar highly branched of both chickpea and lentil.In particular, the STP1 contributes to the regulation of the genes involved in shoot branching via carbon partitioning in Arabidopsis (Cordoba et al., 2015;Otori et al., 2019).In addition, STP1 is also a regulator of glucose, abscisic acid, and stress signaling (Avonce et al., 2004;Cordoba et al., 2015).The constitutive overexpression of the STP1 gene reduced plant growth and branching while the knockout mutant plants showed a phenotype similar to the wild-type plants (Otori et al., 2019).Therefore, these collective data revealed that several genes of trehalose-6-phosphate pathway are closely associated with plant branching modulation in chickpea and lentil, and are suggested as suitable targets for branching-directed biotechnological tools.

Broad hormonal changes
The auxin, cytokinin, and strigolactones are the major hormones involved in plant branching, while other plant hormones such as ABA, JA, and brassinosteroids act indirectly on the modulation of branching and plant growth (Ongaro and Leyser, 2007;Ferguson and Beveridge, 2009).In this context, auxin moves down the dominant shoot and stem to prevent the formation of new buds and branches, while cytokinin promotes meristem activity and bud growth (Müller and Leyser, 2011).In turn, in addition to acting mainly in signaling to plant defense against biotic and abiotic stresses, ABA, salicylic acid, and JA act by inhibiting plant branching (Wasternack, 2015;Yao and Finlayson, 2015;Li et al., 2022).Meanwhile, strigolactones act mainly by regulating branching, which can also be linked to resilience towards stresses (Wang et al., 2015;Wallner et al., 2017;Sun et al., 2022).In turn, brassinosteroids act by promoting an increase in cell volume in the meristem and control multiple processes related to bud outgrowth, branching, and apical dominance (Wei and Li, 2020;Xia et al., 2021).In contrast, ethylene acts mainly in the formation of lateral roots, inhibiting leaf and shoot growth, and regulating plant senescence, while gibberellin acts in seed germination, root and shoot elongation, flowering, fruit patterning, and regulating positively or negatively the axillary bud development (Dubois et al., 2018;Katyayini et al., 2020).In general, all these hormones work in a complex signaling network in a highly interconnected and finely regulated way, depending on the environmental context, plant stage, and plant tissue.Therefore, the action of these hormones in lateral branching and apical dominance is highly complex (Müller and Leyser, 2011;Kebrom, 2017).Herein, it was observed that several transcripts involved in the biosynthesis, signaling, or degradation of all these hormones mentioned above were differentially modulated between apical and axillary buds and contrasting cultivars of chickpea and lentil.In this context, there was less differential modulation of these transcripts in the apical buds of chickpea cultivar lower branched compared to the axillary buds of the same cultivar, with most of these transcripts being involved in the degradation of hormones that inhibit branching.In contrast, there was greater differential modulation of these transcripts in the apical buds of chickpea cultivar highly branched compared to the axillary buds of the same cultivar, with most of these transcripts being involved in the signaling and degradation of different hormones.In the same sense, in the comparison between different tissues and contrasting cultivars of chickpea, several up-or down-regulated transcripts were observed, indicating that there is a significant difference at the hormonal level between these contrasting cultivars of chickpea.In lentil, while there was negative regulation of several of these transcripts involved in the hormonal pathway in the apical buds compared to the axillary buds of the cultivar lower branched, in the cultivar highly branched it was found that there was almost no difference in these transcripts between apical and axillary buds.In the same sense, the number of these transcripts differentially modulated indicated a high difference between contrasting cultivars for both apical and axillary buds.These observations at the hormonal level are in agreement with the fact that multiple pathways regulate bud outgrowth, shoot branching, and apical dominance (Ongaro and Leyser, 2007;Ferguson and Beveridge, 2009;Beveridge et al., 2023).Furthermore, the fact that apical dominance is reduced in cultivars highly branched of chickpea and lentil, there is a tendency for there to be greater hormonal activity in axillary and apical buds (Müller and Leyser, 2011;Cao et al., 2023).Therefore, these collective data revealed that hormonal changes are evident between contrasting cultivars of chickpea and lentil and that there may be key transcripts involved in plant branching and apical dominance of these cultivars.
In our RNA-seq datasets, 15 and 11 main differentially expressed transcripts annotated as involved in cytokinin and auxin signaling pathways of chickpea and lentil, respectively, were identified.These differentially expressed genes play notable roles in hormone perception, signaling, transport, biosynthesis, and degradation, indicating that these expression modulations can contribute to the regulation of axillary branching versus apical dominance in contrasting cultivars of these two crops.The high expression levels of CaCKX3, CaAHK1, CaLOG3, CaAHP1/2/4, CaARR1, CaABCG21, CaCYP735A1 genes, involved in the cytokinin pathway, and CaAux/IAA2/14, CaYUC10, CaPIN2, and CaILR1 genes, involved in auxin pathway, in axillary buds were associated with higher axillary branching in chickpea.Furthermore, the lower expression levels of CaLOG3, CaAHP1, CaAHP4, CaPIN2, CaILR1, and CaAux/IAA2 genes in apical buds were also associated with the reduced apical dominance and higher axillary branching in chickpea.Likewise, the high expression levels of LcAHK1, LcARR12, and LcTMK1/3 genes, and lower expression levels of LcZOG1, LcAux/LAX1/2, and LcTMK2 genes in axillary buds were associated with higher axillary branching in lentil.Meanwhile, the high expression levels of LaAHK1, LcARR2, and LcTMK1/3 genes, and lower expression levels of LcCYP735A1, LcZOG1, LcPILS1, LcAux/LAX1/2, LcTMK2, and LcAux/IAA14 genes in apical buds were associated with the reduced apical dominance and higher axillary branching in lentil.
The transgenic overexpression of AtCKX3 gene resulted in Arabidopsis plants with the phenotype of cytokinin-deficient plants and alteration in plant growth and development compared to wild-type control plants (Dello Ioio et al., 2012).Likewise, the transgenic overexpression of AtAHK gene resulted in Arabidopsis plants with altered cytokinin perception and signaling, consequently, showing affected growth and development (Bartrina et al., 2017).Mutant Arabidopsis plants for T-DNA insertion within the AtLOG3 gene were less sensitive to cytokinin and showed phenotypic changes in plant development (Kuroha et al., 2009).Similarly, mutant Arabidopsis plants for T-DNA insertion within the multiple AtAHP genes showed reduced sensitive to cytokinin and altered development phenotype, indicating that these genes act redundantly as positive regulators of cytokinin signaling (Hutchison et al., 2006).The transgenic overexpression of different AtARR genes results in Arabidopsis plants with a variety of cytokinin-associated phenotypes (Osakabe et al., 2002;Ren et al., 2009).The Atabci19/abci20/abci21 triple and Atabci20/abci21 double knockout Arabidopsis mutants showed hypersensitive to cytokinin and altered plant development, indicating that AtABCG21 acts by fine-tuning the cytokinin response (Kim et al., 2020).The Jatropha curcas Jccyp735a-knockout mutant plants generated by genome editing showed retarded plant growth and altered trans-zeatin and trans-zeatin-riboside metabolism and changed cytokinin signaling pathway (Cai et al., 2018).The constitutive overexpression of ZOG1 gene in transgenic maize and tobacco resulted in cytokinin-deficient plants, growth retardation, delayed senescence, and tasselseed formation (Martin et al., 2001;Rodo et al., 2008).
Meanwhile, transgenic overexpression of different Aux/IAA genes caused several auxin-related altered phenotypes in Arabidopsis and rice plants (Sato and Yamamoto, 2008;Song and Xu, 2013).Transgenic overexpression or triple and quadruple knockout mutants of YUC genes altered auxin biosynthesis and transport in Arabidopsis and influenced plant growth and development (Cheng et al., 2006;Munguıá-Rodrıǵuez et al., 2020).The AtPIN3 and AtPIN6 genes overexpression in Arabidopsis and tobacco plants enhanced auxin efflux, promoted auxin unbalance, and altered plant development, branching, and apical dominance (Lee and Cho, 2006;Cazzonelli et al., 2013).Arabidopsis plants with loss-of-function of ILR genes showed reduced sensitivity to auxin (Rampey et al., 2006).In contrast, transgenic overexpressing of the ILR1 gene in tomato plants resulted in several phenotype alterations, including branching and growth of internodes (Wang et al., 2021b).Likewise, transgenic overexpression or loss-of-function assays showed that TMK transmembrane receptors are essential to auxin perception and signaling, and regulate differential growth and apical dominance (Cao et al., 2019;Marquès-Bueno et al., 2021).The transgenic overexpression of different PILS genes in Arabidopsis interferes with nuclear auxin signaling and plant growth and development (Sun et al., 2020;Feraru et al., 2022).Thus, these previous studies reveal the functional complexity of these genes identified as differentially expressed in our chickpea and lentil datasets.Furthermore, these studies indicate the narrow possibilities of using these highlighted genes related to cytokinin and auxin pathways in biotechnological tools to modulate the branching of these two crops.Therefore, these collective data indicate that the balance of cytokinin and auxin between axillary and apical buds is a determining factor for the regulation of plant branching in both chickpea and lentil.

Strigolactones signaling pathway
Strigolactones promote ubiquitination of SCF MAX2 /D14/SMXL protein complex, which is recognized by the 26S proteasome and directs to degradation, unlocking strigolactone-dependent signal transduction and releasing BRANCHED 1 (BRC1) transcription factor (Zhou et al., 2013;Wang et al., 2015;Bennett et al., 2016).In turn, BRC1-mediated downstream signaling leads to an inhibition of branching, while BRC1 inactivity causes an increased level of branching.Therefore, the presence of strigolactones and BRC1 at higher levels inhibits plant branching.To better understand this signaling pathway, CCD subfamily proteins are major players involved in the strigolactones biosynthesis (Basso et al., 2023), while SMAX/SMXL family proteins are involved in the strigolactone signaling pathway (Basso et al., 2024a), which a part of them is directly linked with the BRC1 transcription factor (Aguilar-Martıńez et al., 2007;Bennett et al., 2016;Seale et al., 2017).In this way, BRC1 acts as one of the main players in this signaling pathway modulating the transcriptional activation of several downstream genes involved in plant branching.Also, other secondary partner proteins act as negative regulators of BRC1 and indirectly influence plant branching (Wang et al., 2019).Among them negative regulators, TiE1, LAP1, and BES1 proteins interact and inhibit BRC1, promoting an increase in plant branching (Yang et al., 2018;Diao et al., 2019;Hu et al., 2020;Maurya et al., 2020).In turn, the CARBOXYLESTERASE 15 enzyme (CXE15) acts in the strigolactones catabolism (Xu et al., 2021).Herein, the CaCCD2 and CaSMXL7 genes were up-regulated and associated with reduced chickpea branching, while the CaSMXL2 gene up-regulation in the apical buds was associated with an increase in axillary branching.Meanwhile, the LcCCD1, LcCCD5, LcSMXL3, and LcSMXL7 genes up-regulation in apical buds was associated with an increased in axillary branching of lentil, and LcBRC1 gene down-regulation in apical buds was associated with a decreased in axillary branching.Therefore, several chickpea and lentil genes of the strigolactones pathway are potentially involved in the modulation of plant branching and suggested as targets for tissue-specific modulation via transgenesis with tissuespecific promoters and gene knockout using genome editing tools.Previous studies showed that the transgenic overexpression of some CCD genes resulted in reduced plant branching while gene knockout increased plant branching, in particular, CDD genes involved in strigolactones biosynthesis (Snowden et al., 2005;Ren et al., 2020;Wang et al., 2021a;Hao et al., 2023).On the other hand, the CaMXL2 and LcSMXL3 genes based on orthologue analysis were previously suggested as involved in the phloem formation independently from strigolactone signaling, while CaSMXL7 and LcSMXL7 genes were suggested as involved in the regulation of shoot branching and elongation (Basso et al., 2024a).Mutant plants for these SMXL genes involved in the strigolactones-and karrikinsindependent pathway showed poor phloem formation, altered sugar accumulation, and seedling lethality (Wallner et al., 2017;Hardtke, 2023;Wallner et al., 2023).As already mentioned, the degradation of the complexed SMXL6,7,8 proteins mediated by strigolactones leads to the activation of the BRC1 signaling pathway to inhibit plant branching (Wang et al., 2015).The overexpression or knockout of the SMXL7 gene has been shown to alter the number and growth of branches in Arabidopsis (Liang et al., 2016).In addition, SMXL7 was also shown as a transcription suppressor in Arabidopsis by binding to SnRK2.3 and SnRK2.6 promoters, which are positively involved in ABA-mediated response to drought stress (Korek and Marzec, 2023;Lian et al., 2023).Similarly, the BRC1-mutant plants displayed a higher number of branches (Aguilar-Martıńez et al., 2007;Gonzaĺez-Grandıó et al., 2013), while BRC1 gene overexpression in transgenic lines resulted in plants with reduced branching (Ding et al., 2020;Maurya et al., 2020;Min et al., 2021).Therefore, several leading candidate genes of the strigolactones signaling pathway were highlighted for further use in genetic engineering to improve chickpea and lentil architecture.

Branching-related transcription factors and major proteins
Several major effect transcription factors and proteins have already been identified as involved in the positive or negative regulation of plant branching (Zhang et al., 2022;Yang et al., 2023).Among these, a group of 16 highly interconnected members, as well as other notable members involved in branching, were monitored in this study.Among these members, the CaEXB1, CaBAS1, CaAGL8, CaWOX4, CaHB21, CaHB40, and CaHB53 proteins were identified as associated with differential branching between contrasting cultivars of chickpea.Similarly, the LcLOF2, LcAS1, LcHB53, and LcPIF4 proteins were also identified as associated with plant branching between contrasting cultivars of lentil.However, these transcription factors have not yet been functionally characterized in chickpea and lentil, but their orthologues in Arabidopsis have been extensively studied.In particular, the EXB1 protein is a WRKY transcription factor that positively regulates the shoot branching by transcriptionally modulating RAX genes in Arabidopsis (Guo et al., 2015).The RNAi-mediated down-regulation of EXB1 resulted in Arabidopsis plants with fewer branches, while the transgenic overexpression resulted in increased branching (Guo et al., 2015;Yu et al., 2016).In addition, EXB1 was shown as modulated by abiotic stress conditions (Guo and Qin, 2016;Yu et al., 2017).Meanwhile, BAS1 is an enzyme modulated by auxin with capacity of inactivate brassinosteroids, which is up-regulated by LOB1 to accumulate low levels of brassinosteroids and reduce cell volume in the boundary zone and, consequently, regulate hypocotyl elongation and plant branching (Neff et al., 1999;Turk et al., 2005;Youn et al., 2016), while LOB1 transcription is modulated by brassinosteroids in Arabidopsis (Bell et al., 2012;Gendron et al., 2012).The negative modulation of brassinosteroid levels resulted in plants with typical brassinosteroid-deficient phenotypes (Han et al., 2017).In contrast, AGL8 (also known as FRUITFULL) is an Agamous-like MADS-box protein accumulated in apical meristems, negatively modulated by APETALA1 (formerly known as AGL7), which acts by regulating the transition between vegetative phase to reproductive phase, cell differentiation during Arabidopsis fruit development, and inflorescence architecture (Mandel and Yanofsky, 1995;Gu et al., 1998;Ferrańdiz et al., 2000;Melzer et al., 2008;Paull et al., 2023).In turn, APETALA1 regulates the expression of several genes involved in floral development and plant branching (Winter et al., 2015;Goslin et al., 2017).In this context, AGL8 controls SAUR10 gene expression to regulate Arabidopsis growth and architecture, and AGL8 overexpression or knockout significantly alters plant architecture (Bemer et al., 2017;Führer et al., 2020).
The WOX4 is a WUSCHEL-related HOMEOBOX protein that regulates the cell division and stem cell maintenance in procambium/cambium (Hirakawa et al., 2010;Nakata et al., 2012;Dolzblasz et al., 2016;Kucukoglu et al., 2017).The WOX4 gene expression is down-regulated by the BES1 transcription factor, which develops antagonistic roles in shoot branching and cambium differentiation linked by the strigolactones signaling pathway (Hu et al., 2021).The RNAi-mediated down-regulation of the WOX4 gene resulted in Arabidopsis plants with reduced vascular development and overaccumulate undifferentiated ground tissue, while the overexpression conferred a hypervascularization phenotype in tomato plants (Ji et al., 2009;Zhang et al., 2019).The Malus domestica WOX4-2 gene overexpression significantly enhanced adventitious shoots in transgenic tobacco and regulated adventitious shoot regeneration in transgenic apple trees (Dong et al., 2022b).Meanwhile, the HB21, HB40, and HB53 genes act redundantly as Homeobox transcription factors to inhibit branching and are positively regulated transcriptionally by BRC1 and SMAX1 (Zheng et al., 2021;Dun et al., 2023;van Es et al., 2024).They are expressed in axillary buds and in stomata guard cells and enhanced by low R:FR light, repress shoot branching, and directly co-regulate NCED3 gene expression and ABA levels in Arabidopsis buds (O'Malley et al., 2016;Gonzaĺez-Grandıó et al., 2017).In this context, Arabidopsis plants with different combinations of mutants of these four genes showed a high number of axillary buds and longer hypocotyls (Gonzaĺez-Grandıó et al., 2017;Dong et al., 2022a;Sańchez-Gerschon et al., 2023).
The LOF2 is a LATERAL ORGAN FUSION transcription factor of the MYB family, positively transcriptionally regulated by the auxin transporter ABCB19 at the boundaries of lateral organs, that acts in the separation of lateral organ and axillary shoots, and initiation of axillary meristem in Arabidopsis and tomato (Lee et al., 2009;Naz et al., 2013;Zhao et al., 2013).The LOF2 gene has a high sequence identity and is closely related to LOF1, both share redundant functions.The lof1/lof2 double mutant plants have stronger defects in axillary meristem formation and organ separation (Lee et al., 2009), while the LOF gene overexpression resulted in dwarfed Arabidopsis plants (Gomez et al., 2011).Similarly, AS1 is an ASYMMETRIC LEAVES transcription factor of the MYB (SANT) family, that accumulates around vascular tissues in cotyledonary and leaf primordia, and in developing leaves, and acts in leaf development and negative regulation of branching in Arabidopsis (Byrne et al., 2000;Sun et al., 2002;Ikezaki et al., 2010).The AS1 and AS2 proteins bind to promoter regions and repress the KNOXI gene family, both involved in plant branching regulation (Guo et al., 2008;Lodha et al., 2013).The as1 mutant plants exhibit severe pleiotropic phenotypes, in particular, elevated frequency of adventitious shoot formation (Semiarti et al., 2001;Xu et al., 2003;Ikezaki et al., 2010;Husbands et al., 2015).The AS1 gene overexpression resulted in the formation of narrower and more elongated leaves, and a greater number (Theodoris et al., 2003).In turn, the PIF4 is a PHYTOCHROME-INTERACTING FACTOR transcription factor of the bHLH family that acts to regulate microtubule organization to mediate high temperatureinduced hypocotyl cell elongation in Arabidopsis (Zhou et al., 2023).In addition, PIF4 together with PIF5 also regulates axillary branching via bud abscisic acid and stem auxin signaling, and induces dark-and stress-induced senescence in Arabidopsis, but is also negatively regulated by ELF3 and CRY1 (Sakuraba et al., 2014;Holalu et al., 2020;Zhai et al., 2020;Li et al., 2021Li et al., , 2024)).The pif4/ pif5 mutant plants exhibit delayed senescence while PIF4 gene overexpression promotes leaf senescence and increases branching (Sakuraba et al., 2014;Zhai et al., 2020;Li et al., 2021).Therefore, these collective data based mainly on functional analysis of orthologs in Arabidopsis revealed several leading candidate genes for use in genetic engineering from transgenesis or genome editing aimed at improving chickpea and lentil architecture.Moreover, two putative branching-associated QTLs were suggested to occur in chickpea.

Conclusion
In this study, the global transcript expression profile of two contrasting chickpea and lentil cultivars with plant architecture phenotype of little versus highly branched was revealed.A total of 1,624 and 2,512 transcripts were identified as differentially expressed between apical and axillary tissues and different contrasting cultivars of chickpea and lentil, respectively.These differentially expressed transcript sets were responsible for modulating several biological processes such as cell cycle, DNA transcription, energy metabolism, broad hormonal biosynthesis and signaling, proteolysis, and vegetative development between different tissues and contrasting cultivars of chickpea and lentil.In particular, the CaEXL2, CaSnRK1/KING1, CaCCD2, CaSMXL2, CaSMXL7, CaEXB1, CaBAS1, CaAGL8, CaWOX4, CaHB21, CaHB40, and CaHB53 genes in chickpea, and LcEXL2, LcSnRK1/KING1, LcSMXL7, LcBRC1, LcLOF2, LcAS1, LcHB21, LcHB53, and LcPIF4 genes in lentil were considered as main players involved in differentially regulate the plant branching between contrasting cultivars.Therefore, since each plant species has a particular and multi-mechanistic regulation at the level of gene expression and function associated with branching modulation (Guo et al., 2020), these collective data will contribute to understanding the general molecular mechanism that modulates branching in the chickpea and lentil.Furthermore, several putative high-effect genes associated with the chickpea and lentil branching are highlighted as potential targets for manipulation through genome editing and transgenesis aiming to improve plant architecture.
FIGURE 1Correlation analysis among different samples of chickpea and lentil based on transcript expression values and number of differentially expressed transcripts in each pairwise comparison for both chickpea and lentil genotypes and tissues.MDS analysis of the 23 RNA-seq datasets for (A) chickpea and (B) lentil samples.Percentages represent variance captured by each principal component 1 and 2 in each analysis.Comparison between (C) chickpea cv.Blanco lechoso (B; little branched cultivar) and cv.FLIP07-318C (F; highly branched cultivar), (D) lentil cv.Castellana (Cs; little branched cultivar), and cv.Campisi (Cs; highly branched cultivar).BX: Blanco lechoso axillary bud, BA: Blanco lechoso apical bud, FX: FLIP07-318C axillary bud, FA: FLIP07-318C apical bud, CsX: Castellana axillary bud, CsA: Castellana apical bud, CmX: Campisi axillary bud, and CmA: Campisi apical bud.Only transcripts with FDR <0.05 and log(fold change) lower than -2 or greater than +2 were considered as differentially expressed transcripts.Venn diagrams of the overlapped differentially expressed transcripts by comparing the contrast between different genotypes and tissues of (E, F) chickpea and (G, H) lentil.The number and percentage of commonly and uniquely differentially expressed transcripts were indicated.

FIGURE 3
FIGURE 3Transcript set enrichment categories for the two pairwise comparisons using the PageMan web tool.The green and red extremes represent the metabolic pathways differentially modulated between contrasting cultivars and tissues of lentil.Only differentially expressed transcripts with FDR <0.05 and log(fold change) lower than -2 or greater than +2 were considered in the pathway analysis.The color intensity is correlated with the statistical significance based on the Wilcoxon test default implemented in the PageMan tool.

TABLE 1
Expression profile of major genes involved in the sucrose-triggered signaling pathway in each pairwise comparison for both chickpea and lentil genotypes and tissues.

TABLE 2
Expression profile of major genes involved in the trehalose-6-phosphate-triggered signaling pathway in each pairwise comparison for both chickpea and lentil genotypes and tissues.

TABLE 3
Expression profile of major genes involved in the cytokinin and auxin signaling pathways in each pairwise comparison for both chickpea and lentil genotypes and tissues.

TABLE 4
Expression profile of major genes of the carotenoids and strigolactones pathway involved in the plant branching in each pairwise comparison for both chickpea and lentil genotypes and tissues.

TABLE 5
Expression profile of major genes and transcription factors involved in the plant branching regulation in each pairwise comparison for both chickpea and lentil genotypes and tissues.