Original Research ARTICLE
Gene Duplication and Transference of Function in the paleoAP3 Lineage of Floral Organ Identity Genes
- Department of Biology, University of Washington, Seattle, WA, United States
The floral organ identity gene APETALA3 (AP3) is a MADS-box transcription factor involved in stamen and petal identity that belongs to the B-class of the ABC model of flower development. Thalictrum (Ranunculaceae), an emerging model in the non-core eudicots, has AP3 homologs derived from both ancient and recent gene duplications. Prior work has shown that petals have been lost repeatedly and independently in Ranunculaceae in correlation with the loss of a specific AP3 paralog, and Thalictrum represents one of these instances. The main goal of this study was to conduct a functional analysis of the three AP3 orthologs present in Thalictrum thalictroides, representing the paleoAP3 gene lineage, to determine the degree of redundancy versus divergence after gene duplication. Because Thalictrum lacks petals, and has lost the petal-specific AP3, we also asked whether heterotopic expression of the remaining AP3 genes contributes to the partial transference of petal function to the first whorl found in insect-pollinated species. To address these questions, we undertook functional characterization by virus-induced gene silencing (VIGS), protein–protein interaction and binding site analyses. Our results illustrate partial redundancy among Thalictrum AP3s, with deep conservation of B-class function in stamen identity and a novel role in ectopic petaloidy of sepals. Certain aspects of petal function of the lost AP3 locus have apparently been transferred to the other paralogs. A novel result is that the protein products interact not only with each other, but also as homodimers. Evidence presented here also suggests that expression of the different ThtAP3 paralogs is tightly integrated, with an apparent disruption of B function homeostasis upon silencing of one of the paralogs that codes for a truncated protein. To explain this result, we propose two testable alternative scenarios: that the truncated protein is a dominant negative mutant or that there is a compensational response as part of a back-up circuit. The evidence for promiscuous protein–protein interactions via yeast two-hybrid combined with the detection of AP3 specific binding motifs in all B-class gene promoters provide partial support for these hypotheses.
Gene duplication has long been interpreted as a potential source of raw genetic material acted upon by evolution (Ohno, 1970; Soukup, 1974; Force et al., 1999). Genes in the ABC model of flower development have been an especially targeted, undergoing multiple duplication events during the course of angiosperm evolution (Theissen et al., 1996; Airoldi and Davies, 2012). Because changes to floral organ identity genes have a profound effect on flower development, they present an ideal system to study the outcome of gene duplication in relation to morphological adaptation (Soltis and Soltis, 2014).
In the model angiosperm Arabidopsis thaliana, the B-class consists of two members, APETALA3 (AP3) and PISTILLATA (PI). Both are necessary in combination with the E-class genes SEPALLATA1–4 (SEP1–4), for petal identity in the second and stamen identity in the third whorl (Bowman et al., 1989, 1991; Coen and Meyerowitz, 1991; Theißen and Saedler, 2001). When B-class function is lost, stamen primordia are homeotically converted into carpels and petal primordia into sepals (Krizek and Meyerowitz, 1996). B-class gene function is highly conserved throughout angiosperms, occurring in core and non-core eudicots as well as monocots (Kim et al., 2004; Zahn et al., 2005; Litt and Kramer, 2010; Di Stilio, 2011). Nevertheless, there are examples of B-class genes being expressed in other plant organs, e.g., in root nodules of alfalfa (Heard and Dunn, 1995) and in first whorl petaloid tepals of tulips (Kanno et al., 2003), suggesting that they may have adopted novel roles in several lineages.
After an ancient duplication leading to the AP3 and PI lineages, in the stem group of the order Ranunculales, two duplication events led to three paralogous lineages of AP3: AP3-I, AP3-II, and AP3-III (Kramer et al., 2003; Figure 1A). Thalictrum thalictroides (Ranunculaceae), a member of the Ranunculid lineage that is sister to all other eudicots (Soltis et al., 2011; Maia et al., 2014), has one PI (ThtPI) and three AP3 orthologs (ThtAP3-1, ThtAP3-2a, and ThtAP3-2b) (Kramer et al., 2003; Di Stilio et al., 2005). The paralog ThtAP3-1 belongs to the AP3-I clade, while ThtAP3-2a and ThtAP3-2b belong to the AP3-II clade and are products of a more recent duplication that likely occurred in the common ancestor of Thalictrum and Aquilegia (Sharma et al., 2011). ThtAP3-2a contains a premature stop, resulting in a truncation affecting the conserved C-terminal motif of the protein; 18 residues encompassing half of the “PI motif-derived” and all the “paleoAP3” motif is missing (Figure 1B; Di Stilio et al., 2005). No AP3-III paralog has been identified so far in Thalictrum by PCR (Di Stilio et al., 2005; Zhang et al., 2013) or by BLAST search of available transcriptomes (unpublished data). Functional studies of the Aquilegia coerulea AP3-III ortholog provide evidence for sub-functionalization of this gene to petal identity (Sharma et al., 2011) and this function appears to be conserved throughout the order, including Papaveraceae (Arango-Ocampo et al., 2016); the lack of an AP3-III ortholog in Thalictrum therefore correlates with the loss of petals in the genus (Di Stilio et al., 2005; Zhang et al., 2013).
FIGURE 1. Simplified B-class gene phylogeny illustrating the position of Thalictrum thalictroides loci (in red) and the comparative structure of their protein products. (A) Simplified phylogeny, modified from Jaramillo and Kramer (2007) and Sharma et al. (2011). An ancient duplication in the angiosperm stem group led to the AP3 and PI lineages (black star), the latter with one representative from T. thalictroides (ThtPI). In the core eudicots, a more recent duplication led to the euAP3 (containing the original APETALA3) and TM6 lineages (white star). In the paleoAP3 lineage, two Ranunculales-wide duplication events (red stars) led to the three paralogous clades AP3-I (including ThtAP3-1), AP3-II (including the more recently duplicated ThtAP3-2a and ThtAP3-2b), and AP3-III (no AP3-III genes have been recovered from Thalictrum). (B) MIKC structure of the three ThtAP3 protein products. ThtAP3-2a is truncated by an early stop codon, resulting in the loss of 18 amino acids, including the PaleoAP3 motif and a portion of the PI motif (Di Stilio et al., 2005).
Petals may be interpreted as adaptive structures that attract biotic pollinators and this function has been transferred, fully or in part, to other organ types multiple times during angiosperm evolution (Cronk et al., 2002). In fact, in the Ranunculaceae, where sepals are often petaloid, petals have been lost independently multiple times with the role of attraction adopted instead by showy sepals (Zhang et al., 2013). In a number of distantly related species, including Aristolochia and Tulipa, heterotopic expression of B-class genes has been proposed as causative of petaloidy of first-whorl organs (van Tunen et al., 1993; Kanno et al., 2003; Jaramillo and Kramer, 2004). In Aquilegia, AqAP3s are not involved in petal identity or development of papillate epidermal cells, although they do contribute to the production of anthocyanin in petaloid sepals (Jaramillo and Kramer, 2007; Sharma et al., 2011; Sharma and Kramer, 2017). Although T. thalictroides flowers lack petals from inception, its sepals have a number of features typically associated with petals: they are non-photosynthetic (white or pink), relatively large (surpassing stamens), they may contain papillate cells in the upper epidermis (Di Stilio et al., 2009) and they express all B-class genes (Di Stilio et al., 2005). Sepals of wind pollinated species such as Thalictrum dioicum, on the other hand, are smaller (shorter than stamens), green, lack papillate cells, and do not express AP3 orthologs (Di Stilio et al., 2005; Soza et al., 2012).
The goal of this study was to conduct a functional analysis of the three AP3 orthologs in T. thalictroides, a ranunculid with representatives of the paleoAP3 lineage of B-class genes. We aimed to determine the degree of redundancy versus divergence amongst these paralogs, while comparing their role to the more widely characterized euAP3 lineage. Finally, we investigated whether one or more of these loci are involved in ectopic petaloidy, in the form of partial transference of petal function to sepals, in the insect-pollinated species T. thalictroides. We addressed these questions via targeted silencing of individual genes, by determining the ability of each protein product to dimerize and by identifying AP3 binding sites within promoter regions of all four B-class genes.
Materials and Methods
Partial coding sequences for ThtAP3-1, ThtAP3-2a, and ThtAP3-2b were obtained from GenBank (AY162886, AY162887, and AY162888; Kramer et al., 2003). Full coding sequences were obtained from a 1KP T. thalictroides transcriptome1. Full genomic sequences and promoter regions were obtained from a T. thalictroides reference genome (unpublished) and deposited in GenBank (MG889397, MG889396, and MG889395).
Thalictrum thalictroides bare root plants were purchased from nurseries and grown in the University of Washington (UW) Greenhouse under ambient conditions from mid-February through mid-May. A voucher specimen is deposited at the UW Herbarium (V. Di Stilio 123, WTU 376542).
Virus-Induced Gene Silencing
Regions for targeted gene silencing of Thalictrum AP3 genes were selected to exclude areas with more than 13 continuous homologous base pairs among the three paralogs (gene duplicates). Fragments were amplified by PCR from a representative clone using primers with added BamHI and KpnI restriction sites (Supplementary Table S1), ligated to linearized tobacco rattle virus vector (TRV2; Liu et al., 2002) and transformed into Agrobacterium tumefaciens strain GV3101. The TRV2-ThtAP3-1 construct was prepared using a 429 bp fragment comprising the C-terminal region (282 bp) and 3′UTR (147 bp) of ThtAP3-1. The TRV2-ThtAP3-2a construct consisted of a 427 bp fragment comprising the C-terminal region (227 bp) and 3′UTR (200 bp) of ThtAP3-2a. The TRV2-ThtAP3-2b construct consisted of a 408 bp fragment comprising the C-terminal region (253 bp) and 3′UTR (155 bp) of ThtAP3-2b. Additional experiments targeting shorter regions (216–342 bp) were attempted first, but they did not trigger sufficient down-regulation. Experiments using double and triple constructs were also attempted unsuccessfully.
Twenty T. thalictroides tubers that had been kept in soil in the dark at 4°C for 8 weeks, were treated with each construct as described previously (Di Stilio et al., 2010; Galimba et al., 2012). Briefly, a small incision was cut in the tubers near the bud using a clean razor blade, they were then submerged in infiltration medium containing appropriate Agrobacterium cultures (TRV1 and one of the TRV2 constructs), and infiltrated in a chamber under full vacuum (-100 kPa) for 10 min. Nine TRV2-ThtAP3-1, five TRV2-ThtAP3-2a, and 12 TRV2-ThtAP3-2b treated plants survived to flowering. Twenty plants were infiltrated with empty TRV2 vector (mock-treated control, to detect background viral effects). All plants were transferred to the greenhouse following infiltration and were grown together with 20 untreated plants under equal conditions. Leaves and flowers arose approximately 2 weeks later. Flowers from all treatments and controls (untreated and treated with empty vector) were observed, as they opened, under a Nikon SMZ800 dissecting scope, photographed using a Q-Imaging MicroPublisher 3.3 digital camera or a Canon PowerShot SD890 IS digital camera, and flash-frozen for RNA processing.
Molecular Validation of VIGS Lines
After recording their phenotype and photographing, young open flowers that had been flash frozen (as described above) were processed to determine the presence of TRV1 and TRV2 constructs, and the expression levels of B-class genes, including the three Thalictrum AP3 genes and the single copy gene ThtPI. Total RNA was extracted using TRIzol (Invitrogen, Life Technologies, CA, United States), following manufacturer instructions and DNased using amplification grade DNase (Invitrogen, Life Technologies, CA, United States). First strand cDNA synthesis was carried out on 1 μg of total mRNA using iScript (Bio-Rad, CA, United States), following manufacturer instructions, and diluted 2.5-fold for use in quantitative reverse transcriptase (RT) PCR (qPCR). PCR was carried out with GoTaq (Promega, WI, United States) on 1 μl of cDNA using TRV1- and TRV2-specific primers (Supplementary Table S1) for 30 cycles at 51°C annealing temperature. Locus-specific primers, designed to amplify regions distinct from those used in the virus-induced gene silencing (VIGS) constructs, were used to test expression levels of ThtAP3-1, ThtAP3-2a, ThtAP3-2b, and ThtPI by qPCR (Supplementary Table S1). Primers were validated prior to use, using a cDNA dilution series to verify consistent efficiencies and a dissociation curve analysis to confirm single product amplification, as previously published (Galimba et al., 2012). Each qPCR reaction contained 15 μl iQ SYBR Green Supermix (Bio-Rad, CA, United States), 12.2 μl H2O, 0.9 μl each of forward and reverse primer and 1 μl of cDNA. Samples were amplified on an MJ Research Chromo4 Detector for 45 cycles, in triplicate, including a no-template control. Cycling conditions were: 94°C for 10 min and 45 cycles of 94°C for 30 s, 53°C for 30 s, and 72°C for 30 s. Relative expression was calculated using the 2-ΔΔCt method (Livak and Schmittgen, 2001), and normalized against the averaged expression of two housekeeping genes, ThtACTIN and ThtEF1α (Elongation Factor 1α). Since B-class gene expression levels between untreated (n = 6) and empty TRV2-treated flowers (n = 3) were not significantly different in a Student’s two-tailed t-test with unequal variance (p > 0.05), both controls were combined for further analyses. The statistical significance of differences in gene expression between controls and treatments was calculated using Student’s two-tailed t-test with unequal variance: controls (n = 9), TRV2-ThtAP3-1 (n = 15), TRV2-ThtAP3-2a (n = 10), and TRV2-ThtAP3-2b (n = 4), and p-values were evaluated using Holm–Bonferroni corrections to avoid Type I error.
Yeast Two-Hybrid Assays
To prepare constructs for yeast two-hybrid analysis, complete coding sequences for ThtAP3-1, ThtAP3-2a, and ThtAP3-2b were cloned into pGADT7 and pGBKT7 vectors using the In-Fusion HD Cloning Kit (Clontech, CA, United States) and custom primers (Supplementary Table S1). The pGADT7 and pGBKT7 constructs for the E-class interacting partner ThtSEP3ΔC were available from a previous study (Galimba et al., 2012). ThtSEP3ΔC is a C-terminal-truncated version of ThtSEP3 lacking the last 195 bp of coding sequence to avoid auto-activation (Causier and Davies, 2002; Galimba et al., 2012); C-terminal truncation is supported by a number of studies showing that the K domain is more critical for MADS-box protein interactions (Davies et al., 1996; Pelaz et al., 2001; Immink et al., 2009) and is involved both in dimer and tetramer formation (Puranik et al., 2014).
Yeast two-hybrid assays were carried out using Matchmaker Gold Yeast Two-Hybrid System (Clontech, CA, United States). Cells were co-transformed and plated on Leu/Trp-free media to select for diploid colonies. Single colonies were serially diluted 10-fold to 1:10,000 in water and 5 μl of each dilution were plated on Leu/Trp/His-free media and Leu/Trp/His-free media supplemented with Aureobasidin A (AbA) to test for protein interaction, and on Leu/Trp-free media to control for yeast growth. Interactions were scored and photographed using a Canon PowerShot SD890 IS digital camera after 4 days of incubation at 28°C.
Identification of Promoters and APETALA3 Binding Motif Analysis
In A. thaliana, the region extending 496 bp upstream of the AP3 start codon contains three CArG boxes and drives GUS expression in the same temporal and spatial patterns as the AP3 transcript in wild-type flowers (Tilly et al., 1998). Using this information as guideline, and to identify promoters in Thalictrum AP3, a 1 kb fragment upstream of the start codon of each gene was obtained from a T. thalictroides draft genome (unpublished). The Arabidopsis AP3 frequency matrix was downloaded from JASPAR2 (Mathelier et al., 2014; Figure 5A). This matrix, derived from ChIP-seq data (Wuest et al., 2012), consists of nucleotide frequencies at 15 positions: a 10-nucleotide CArG box surrounded by two 5′ and three 3′ nucleotides. The use of frequency matrices provides position-specific penalties for deviations from the consensus as opposed to simpler models, like consensus sequences, which treat all mismatches equally (Stormo, 2013). We converted the matrix to a position-specific scoring matrix (PSSM) using the RSAT-convert-matrix tool available at Regulatory Sequence Analysis Tools3 (Medina-Rivera et al., 2015). The A. thaliana background model estimation method was utilized with default settings. The PSSM was used in MORPHEUS4 (Minguet et al., 2015) to search sections of sequence upstream of the START codon of TthAP3-1, ThtAP3-2a, ThtAP3-2b, and ThtPI for AP3 binding sites. MORPHEUS provides a score for each binding site that is based on the relative affinity of the binding site to the provided matrix, the threshold was set to 5 based on the score distribution histogram (Supplementary Figure S2) to limit the results to the best matching sites.
To visualize the degree of conservation of the T. thalictroides putative AP3 binding motifs (found by the method described above), we generated two alignments of the first 500 bp upstream of the start codon of paleoAP3-1 and paleoAP3-2 orthologs of other available Ranunculaceae. Sequences were retrieved from GenBank and Phytozome (Supplementary Table S2 and Supplementary Figure S3), aligned using MUSCLE (Edgar, 2004) and CLC Main Workbench 7 (Qiagen), and homologous regions to the T. thalictroides AP3 binding sites were identified.
Analysis of Protein Structure
In order to identify the alpha helices known to be critical for MADS box gene functionality (Puranik et al., 2014), and to test whether any of these were lacking in the paralog coding for a truncated AP3 (ThtAP3-2a), we analyzed the protein structure of the region comprising the end of the I domain through the C domain of the three Thalictrum AP3 proteins using Protein Homology/analogY Recognition Engine v 2.0 (Phyre2; Kelley et al., 2015).
Targeted Gene Silencing of Three T. thalictroides AP3 Orthologs
To investigate the function of three B-class gene orthologs of the ranunculid T. thalictroides, we conducted targeted VIGS using single gene constructs, analyzed gene expression of treated plants in relation to untreated and empty vector controls, and compared the resulting floral phenotypes.
Flowers treated with empty TRV2 vectors and verified for the presence of TRV1/2 transcripts (Supplementary Figure S1) were combined with untreated wild-type flowers, and used as a control treatment for molecular validation (n = 9 flowers from four plants; Figure 2). Wild-type T. thalictroides flowers are apetalous, with 5–12 white or pink petaloid sepals enclosing 45–76 filamentous stamens and 3–11 free carpels with prominent papillae at the stigma (Di Stilio et al., 2009; Galimba et al., 2012; Figure 3A). Wild-type leaves are compound with lobed leaflets (Figure 3B). Empty TRV2-treated flowers showed comparable morphology to wild-type (Figure 3C). Small sections of brown necrotic tissue were present on 19% of treated flowers, similar to previously reported background viral effect (Di Stilio et al., 2010), and these were therefore not counted as phenotype.
FIGURE 2. Molecular validation of targeted gene silencing of Thalictrum thalictroides AP3 orthologs. (A–D) Left panels: Quantitative RT-PCR (qPCR) showing average relative expression levels of ThtAP3-1 (A), ThtAP3-2a (B), ThtAP3-2b (C), and ThtP1 (D) in each of three treatments, TRV2-ThtAP3-1, TRV2-ThtAP3-2a, and TRV2-ThtAP3-2b by virus-induced gene silencing. Control (n = 9: untreated, n = 6 plus TRV2-empty, n = 3); ThtAP3-1 VIGS (n = 15); ThtAP3-2a VIGS (n = 10); and ThtAP3-2b VIGS (n = 4). Gene expression levels of the control were set to 1. Expression was normalized against ThtACTIN and ThtEEF1. Mean and SE of biological replicates are shown; different letters indicate a significant difference in Student’s two-tailed t-test with unequal variance and Holm–Bonferroni corrections (p ≤ 0.05). (A–C) Right panels: Molecular validation of targeted gene silencing in individual flowers (labels represent plant number, followed by flower number) relative to control (set to 1). Treatment average (dotted bar) of individual flowers (biological replicates). SE shown for control and treatment average values. Black bars indicate flowers shown in Figure 3. Asterisks cross-reference same treatment averages compared between treatments (left), or amongst individual samples within a treatment (right).
FIGURE 3. Phenotypes resulting from targeted silencing of Thalictrum thalictroides AP3 orthologs. (A) Untreated T. thalictroides representative flower. (B) Untreated representative leaflet. (C) Flower treated and validated for empty TRV2 vector. (D–J) Representative flowers treated with and validated for TRV2-ThtAP3-1. (D) Flower with narrow sepals. (E) Flower with chimeric organ (boxed) and extra inner sepals (arrows). (F) Detail of sepal/stamen chimera in panel (E) (arrow). (G) Flower with small, curved sepals and chimeric organ in place of outer stamen (boxed). (H) Detail of sepal–carpel chimera in panel (G), with stigma (arrow). (I) Flower with small, curved, greener sepals, green segments indicated by white arrows, and smooth stigmas, indicated with black arrows. (J) Flower with smooth stigmas, three indicated with arrows. (K–N) Representative flowers treated with TRV2-ThtAP3-2a. (K) Flower with chimeric sepal/stamen organ in place of outer stamen (arrow). (L) Flower with extra inner sepal (arrow). (M) Flower with lobed sepal (arrow). (N) Flower with unfused carpel and exposed ovule (arrow). (O–R) Representative flowers treated with TRV2-ThtAP3-2b. (O) Flower with lobed sepal with green sectors (arrow). (P) Flower with chimeric organ (boxed) and extra inner sepals (arrows). (Q) Detail of sepal/stamen chimera in panel (O). (R) Flower with narrow sepals and stunted stamens exhibiting small anthers and short filaments (arrows). (S) Percentage of flowers exhibiting each phenotype (from plants verified for TRV1/2 transcripts): TRV2-ThtAP3-1 (n = 24); TRV2-ThtAP3-2a (n = 15); and TRV2-ThtAP3-2b (n = 27). Sample labels represent plant number, followed by flower number (see Figure 2 for individual expression levels of target genes). Scale bar = 1 mm.
Flowers treated with TRV2-ThtAP3-1 and verified for the presence of TRV1/2 transcripts (n = 15 flowers from four plants; Supplementary Figure S1) exhibited a significant down-regulation of ThtAP3-1 transcripts, with an average 5.3-fold decrease in gene expression levels with respect to controls (p < 0.001, Figure 2A). Down-regulation of ThtAP3-1 at the individual level ranged from a 1.5- to 32-fold decrease in gene expression (Figure 2A). Average expression levels of the other three B-class genes were statistically like controls (Figures 2B–D and Supplementary Table S3). All flowers (n = 24) from validated plants were phenotyped (Figure 3S). Abnormal phenotypes included narrow sepals in 38% of flowers (Figure 3D), smaller and possibly extra inner sepals, against the outer stamens in 38% of flowers (Figure 3E, sepal number is variable in Thalictrum, but positioning and size of these is distinct) and chimeric organs (sepal/stamen or sepal/carpel) in the sepal/stamen boundary in 13% of flowers (Figures 3E–H). These chimeric organs included sepaloid organs with anther sacs (Figures 3E,F) or sepaloid organs with stigma-like tissue on the distal end (Figures 3G,H). We also observed stunted stamens with small anthers in 42% of flowers and/or short filaments in 54% of flowers (Figures 3D,G,I). Stunted stamens were not present in our empty TRV2-treated flowers, although we have observed them previously at low frequencies in viral controls (Soza et al., 2016). TRV2-ThtAP3-1 treated plants also possessed small sepals on 50% of flowers and/or curved sepals on 63% of flowers (Figures 3G,I). We also observed patches of green tissue on sepals of 13% of flowers (Figure 3I) and smooth stigmas, due to the absence of stigmatic papillae, on 29% of flowers (Figures 3I,J). In summary, in addition to the expected role in stamen identity, down-regulation of ThtAP3-1 altered sepal size (and possibly number), shape and color, changed organ identity at the sepal/stamen boundary and resulted in loss of stigmatic papillae.
Treatment with TRV2-ThtAP3-2a failed to down-regulate ThtAP3-2a in flowers verified for the presence of TRV1 and TRV2 transcripts (n = 10 flowers from three plants; Supplementary Figure S1). On the contrary, it resulted in up-regulation of all ThtAP3s and ThtPI (Figures 2A–D). These flowers showed, on average, a 2.9-fold increase in ThtAP3-2a expression, which was significantly higher than controls (p < 0.001; Figure 2B). Up-regulation of ThtAP3-2a at the individual level ranged from a 1.2- to 4.7-fold increase in gene expression (Figure 2B). They also had, on average, significantly higher gene expression levels than controls for ThtAP3-1 (2.1-fold, p = 0.005; Figure 2A and Supplementary Table S3) and ThtPI (1.8-fold, p = 0.013; Figure 2D and Supplementary Table S3). ThtAP3-2b expression levels were 1.8-fold higher in TRV2-ThtAP3-2a treated flowers; this increase was not significant when applying Holm–Bonferroni corrections (p = 0.026; Figure 2C and Supplementary Table S3). Flower (n = 15) phenotypes from validated plants consisted of a subset of those observed in ThtAP3-1 treated plants (Figure 3S). Sepal/stamen chimeric organs in place of outer stamens were present on 7% of flowers (Figure 3K), and small extra inner sepals were present on 20% (Figure 3L). Lobed sepals were present on 33% of treated flowers (Figure 3M) and were not present in any of the untreated plants. We observed curved sepals on 33% of flowers and stunted stamens with short filaments and/or small anthers on 13% of flowers. We did not observe narrow, small, or green outer sepals in this treatment. Small, underdeveloped carpels with smooth stigmas, including one with an exposed ovule (Figure 3N), were present in 13% of flowers. In summary, we were unable to detect down-regulation of ThtAP3-2a after treatment with TRV2-ThtAP3-2a, and instead detected unexpected up-regulation of all B-class genes (albeit not statistically significant for ThtAP3-2b), which was associated with phenotypes affecting stamen/sepal boundary, sepal morphology, and carpel development.
Flowers treated with TRV2-ThtAP3-2b and verified for the presence of viral transcripts (n = 4 flowers from three plants; Supplementary Figure S1) showed, on average, a strongly significant down-regulation of ThtAP3-2b compared to controls (2.8-fold decreased expression, p = 0.001; Figure 2C). ThtAP3-2b was down-regulated a 4.1- to 7.4-fold at the individual level (Figure 2C). All other B-class gene expression levels were like controls (Figures 2A,B,D and Supplementary Table S3). Flowers (n = 27) from validated plants (Figure 3S) showed lobed sepals on 26% of flowers, with green sectors on 7% of flowers (Figure 3O). Small sepals were also present on 48% of flowers and curved sepals were present on 30%. We also observed stamens replaced with chimeric organs (sepaloid with carpeloid or stamenoid features) on 15% (Figures 3P,Q) and small extra inner sepals on 15% of flowers (Figure 3P). Plants also displayed narrow sepals on 19% of flowers (Figure 3R) and stunted stamens, with short filaments on 30% of flowers and/or small anthers on 11% (Figure 3R). Smooth stigmas with reduced papillae were present on 4% of flowers. In summary, down-regulation of ThtAP3-2b altered sepal size, shape and color, stamen identity, sepal/stamen boundary, and stigmatic papillae development in a similar manner as the down-regulation of ThtAP3-1, with the addition of sepal lobing.
Taken together, phenotypes resulting from VIGS treatments (and not observed in control flowers) affected either sepal, stamen, or carpel morphology. Abnormal sepal morphology occurred in flowers across treatments: down-regulation of ThtAP3-1 and ThtAP3-2b resulted in reduction in overall size and width (small and narrow), shape (curved instead of flat) and color (green), with ThtAP3-2b VIGS flowers also exhibiting sepal lobing. Similar lobing and curving of sepals, was observed in TRV2-ThtAP3-2a treated flowers, which exhibited higher expression of all B-class genes, although none of the additional sepal defects were present (narrower, smaller, or green). The second major category of phenotypes affected stamen morphology across the three treatments: stamens looked stunted, had small anthers, their filaments failed to properly elongate, and outer stamens were sometimes replaced by chimeric organs or small sepals. Lastly, down-regulation of ThtAP3-1 and ThtAP3-2b affected late carpel development, leading to the absence of stigmatic papillae, while the high expression of B-class genes in TRV2-ThtAP3-2a treated flowers caused carpel stunting and failure to fuse around the ovule.
Yeast Two-Hybrid Analyses: Promiscuous Interactions Among Thalictrum B-Class Proteins
To test the interactions among the four B-class proteins present in T. thalictroides, we performed yeast two-hybrid analyses, including the predicted E-class partner protein ThtSEP3 (Figure 4). We used a ThtSEP3ΔC construct with a truncated C-terminus to avoid previously documented auto-activation (Galimba et al., 2012). Control transformations with empty vectors (pGBKT7 and pGADT7) produced minimal to no growth, ruling out auto-activation for the other proteins.
FIGURE 4. Protein–protein interactions among B-class gene products of the ranunculid Thalictrum thalictroides. Interactions between the three ThtAP3 proteins, ThtPI and ThtSEP3 of T. thalictroides were determined with the yeast two-hybrid system. The C-terminus of ThtSEP3 was truncated to avoid autoactivation (ThtSEP3ΔC). (A) Colony growth on selective Leu/Trp/His-free + AbA medium. Yeast cells were spotted in four 10-fold serial dilutions (from left to right) for each interaction tested. All proteins were expressed as fusion with the GAL4 activation domain (AD) and the GAL4 DNA binding domain (BD). pGBKT7 and pGADT7 are empty vector controls. (B) Interpretation of the strength of the protein–protein interactions shown in panel (A). –, no interaction; +, interaction; ++, strong interaction.
As expected, all three ThtAP3 proteins could dimerize with their B-class partner ThtPI, and this interaction was observed in both directions. A more unexpected result was that all three ThtAP3 proteins could heterodimerize with each other: ThtAP3-1 interacted with ThtAP3-2a and ThtAP3-2b, and ThtAP3-2a interacted with ThtAP3-2b. These interactions varied in strength, and ThtAP3-1 and ThtAP3-2a had a positive interaction in one direction and a negative one in the other. ThtAP3-1 interacted weakly with the empty vector in one direction, and this may decrease support for the weak interaction detected between ThtAP3-1 and ThtAP3-2b. Using the yeast culture dilutions (Figure 4A) to interpret the strength of the protein–protein interactions (Figure 4B), we observed that ThtAP3-1 could homodimerize strongly, while ThtAP3-2a and ThtAP3-2b homodimerized weakly and ThtPI did not form homodimers. All four B-class proteins (ThtAP3-1, ThtAP3-2a, ThtAP3-2b, and ThtPI) could interact with the E-class partner ThtSEP3. Taken together, all three ThtAP3 proteins heterodimerize with ThtPI and ThtSEP3, as expected, and additionally homodimerize and heterodimerize with each other.
Identification of Putative AP3 Binding Motifs in T. thalictroides B-Class Gene Promoters
To find additional evidence for auto- and/or cross-regulation of B-class genes by ThtAP3 proteins, we searched for AP3 binding sites in Thalictrum B-class gene promoter regions using a frequency matrix (Figure 5A) derived from experimental binding assays that includes AP3-specific binding frequencies to the CArG box plus five additional nucleotides (Sharma et al., 2011; Sharma and Kramer, 2013), as implemented in MORPHEUS (Minguet et al., 2015). All binding site sequences identified above the threshold (>5, Supplementary Figure S2) are listed in Supplementary Table S4. Three putative AP3 binding sites were identified for ThtAP3-1, located at positions (upstream from start codon) -262, -139, and -121 (Figure 5B). ThtAP3-2a had only one binding site (position -9; Figure 5C), ThtAP3-2b had three (positions -293, -151, and -78; Figure 5D), and ThtPI had one (position -340; Figure 5E). Binding sites at position -121 in the ThtAP3-1 promoter, -91 in the ThtAP3-2a promoter, and -78 in the ThtAP3-2b promoter appear to be homologous based on our alignments with additional ranunculids (Supplementary Figure S3), and are the most conserved. They are 86.7% identical between ThtAP3-1 and ThtAP3-2b, 66.7% between ThtAP3-1 and ThtAP3-2a, and 80% between ThtAP3-2a and ThtAP3-2b (purple boxes in Figure 5F). The other binding sites are locus-specific (Figure 5F). The alignment to orthologs from other Ranunculaceae also shows the conservation of these binding sites within the family, and the sequence divergence between ThAP3-2a and RanAP32-b (Supplementary Figure S3). The AP3-2 alignment reveals that two of ThtAP3-2b motifs have corresponding homologous sequence in ThtAP3-2a (Supplementary Figure S3B), yet they have diverged enough that their MORPHEUS scores (-1 and -3.1) were below the set threshold (Figure 5F, shown in lighter shading), suggesting that they are no longer functional.
FIGURE 5. Location of APETALA3-like binding sites on Thalictrum thalictroides B-class gene promoters. (A) Sequence logo for Arabidopsis AP3 binding frequency matrix (jaspar.genereg.net), with letter sizes relative to nucleotide frequency. (B–E) Positions identified by MORPHEUS as AP3 binding sites, in 1 kb sections of sequence directly upstream of each gene. The height of each vertical bar indicates the MORPHEUS score of that binding site, with the cutoff score set at 5. (F) Schematics of promoter regions for each gene, with binding site positions indicated by bars. A putative homologous binding site shared by all three ThtAP3 promoters is shown in the same color (purple), and two putative homologous regions in ThtAP3-2a are shown in lighter shades (see also Supplementary Figure S3).
Protein structural analysis on amino-acid translations of the coding sequences of all three AP3 loci identified the two alpha helices spanning the I and K domains (Supplementary Figure S4). These helices have been shown to be critical for SEP3 multimerization, and possibly for MADS box protein interactions more generally (Puranik et al., 2014). Despite its C-terminus truncation, ThtAP3-2a appears to possess the required helices for dimer and tetramer formation. The first helix, involved in dimer formation, has six amino acid disparities between the two paralogs; the second helix, involved in tetramer formation (Puranik et al., 2014), has 12 amino acid disparities. Of these, five involve hydrophobic residues in one paralog or the other, and a broader alignment across multiple ranunculid taxa revealed that three of these are specific to AP3-2a protein orthologs (Supplementary Figure S4). Further functional testing, combined with protein crystallography, would be necessary to ascertain potential effects of divergent residues in mediating dimerization or tetramerization between ThtAP3-2a and other MADS-box proteins.
This study investigated the function of three AP3 orthologs representing ancient as well as recent gene duplications in T. thalictroides, a representative of the sister lineage to core eudicots. We enquired whether these gene paralogs have remained redundant or diverged in function, and whether they contribute to ectopic petaloidy of sepals. Down-regulation of two of the paralogs (ThtAP3-1 and ThtAP3-2b) correlated with sepal, stamen, and stigma developmental defects. In addition to the expected interaction with the E-class protein ThtSEP3 and the other member of the B-class lineage ThtPI, all ThtAP3s had the ability to form homodimers and to interact with each other, providing a potential mechanism for novel function. Putative binding motifs were identified in all B-class gene promoters, supporting the potential for cross-regulatory interactions. Based on the evidence presented here, we conclude that, in addition to a conserved role in stamen identity, ThtAP3-1 and ThtAP3-2b contribute to ectopic petaloidy of sepals in this species, as evidenced by their effect on sepal color, shape, and size. They also appear to regulate the genetic pathway leading to stigmatic papillae in carpels. Finally, we propose two working hypotheses to explain the unexpected up-regulation of all B-class genes in plants targeted for silencing of ThtAP3-2a, which codes for a truncated protein.
Prior characterization of Thalictrum AP3 expression found high expression of all three loci in sepals and stamens of T. thalictroides, yet little to no expression in the reduced green sepals of T. dioicum (Di Stilio et al., 2005; LaRue et al., 2013). Together with the phenotypes emerging from our VIGS experiments, these data suggest a combined function of ThtAP3 genes in stamen identity and in the partial transference of petaloid features to perianth organs, otherwise described as sepals based on morphology and evolutionary context (e.g., they have multiple vascular strands, they completely enclose the floral bud throughout development, and petaloid sepals are present throughout the Ranunculaceae). Even though there is no prior expression data for stigmas, our VIGS data suggest that ThAP3 influence the development of stigmatic papillae. The conical/papillate-cell identity gene MIXTA is under the control of B-class genes in Antirrhinum and Phalaenopsis (Perez-Rodriguez et al., 2005; Manchado-Rojo et al., 2012; Pan et al., 2014) and is expressed in stigmatic papillae of Thalictrum (Di Stilio et al., 2009). The loss of stigmatic papillae in carpels of flowers experiencing down-regulation of ThtAP3-1 and ThtAP3-2b in our VIGS experiments suggests that B-class regulation of MIXTA possibly also occurs in Thalictrum.
Petaloid appearance can have different genetic underpinnings, with certain species relying on B-class gene expression for ectopic petaloidy (e.g., tulips; van Tunen et al., 1993; Kanno et al., 2003), while others exhibit petaloid morphology independent of B-class gene expression (e.g., Aristolochia; Pabón-Mora et al., 2015). E-class genes are also known to contribute to petaloid features of sepals in Thalictrum (Soza et al., 2016). Given the presence of petaloid sepals throughout Ranunculaceae, it is unlikely that they arose de novo in Thalictrum. However, Thalictrum AP3s have a distinct role in petaloid morphology of sepals when compared to other ranunculids where it has been characterized: Aquilegia (Sharma and Kramer, 2013) and Nigella (Wang et al., 2015) in the Ranunculaceae and Papaver (Drea et al., 2007) in the Papaveraceae. For example, in Aquilegia, loss of AqPI function results in loss of anthocyanin production in sepals, but does not alter other aspects of sepal morphology (Sharma and Kramer, 2017). Green streaks on sepals in our VIGS experiments are comparable to those found in sepals of Nigella damascena loss-of-B-function mutants, which also lost anthocyanin pigmentation. In spite of this, B genes were not interpreted as playing a role in sepal petaloidy in that system (Wang et al., 2015). In Thalictrum, we interpreted a change toward a more leaf-like appearance of perianth organs, such as change in shape, reduction in size and the gain of photosynthetic pigment, as loss of “petaloid” features. The fact that AP3 and PI negatively regulate genes involved in chlorophyll accumulations resulting in the white A. thaliana petals (Mara et al., 2010), is consistent with our observations of sepal greening during down-regulation of B-class genes in Thalictrum, and points to similar mechanisms for this petaloid feature in petals and sepals. Based on evidence presented here, we propose that the common ancestor of Thalictrum evolved novel interactions among B-class proteins following its lineage-specific ThtAP3-2a/b gene duplication. This, in turn, enabled new regulatory interactions that contributed to sepal petaloidy in conjunction with the E-class partners (Soza et al., 2016). Consistent with this hypothesis, the wind-pollinated species T. dioicum has small, green sepals that do not express the AP3-2 loci early in development (Di Stilio et al., 2005).
Given that orthologs of the A-class gene APETALA1 do not exist in the order Ranunculales (Litt and Irish, 2003), it is likely that the genetic factors involved in Thalictrum sepal identity differ from those in the evolutionarily derived core eudicots. For example, the presence of chimeric outer stamens with combined carpel and sepal features in TRV2-ThtAP3-1 and TRV2-ThtAP3-2b treated flowers could be considered inconsistent with the mutually antagonistic nature of the A- (sepal identity) and C- (carpel identity) classes (Bowman et al., 1991), as defined in the original ABC model. Alternatively, the presence of ectopic carpeloid features may suggest that, like in Arabidopsis, T. thalictroides B-class genes act as suppressors of carpel development genes outside of the carpel zone (Wuest et al., 2012). In Nigella, AP3 homologs function in keeping the stamen–petal boundary (Gonçalves et al., 2013; Wang et al., 2015). The presence of sepal/stamen intermediates in the boundary region between these two organs in Thalictrum knockdowns suggests that, in the absence of petals and of the AP3-3 petal identity gene, the other AP3 paralogs perform a boundary-keeping role between the stamen and perianth zones (sepals, in this case). This observation is consistent with a role of B-class genes in regulating the expression zone of the C-class gene AG in other ranunculids (Lange et al., 2013; Sharma and Kramer, 2017). No carpel–sepal chimeras were observed in plants targeted for ThtAP3-2a silencing, which were actually over-expressing B-class genes. TRV2-ThtAP3-2a treated flowers also never exhibited signs of loss of petaloidy, such as smaller, narrower, or green sepals, and they were the only treatment to cause stunted and unfused carpels, a potential sign of B function disrupting normal carpel identity in the inner floral zone. Presence of other phenotypes, such as stamen–sepal chimeras and lobed sepals, may be explained by an overall disruption of the protein ratios necessary for normal development.
Down-regulation of the ThtAP3 paralogs individually did not result in complete homeotic conversion of stamens into carpels or complete loss of petaloidy, suggesting at least a partial degree of redundancy. This is unlike the single copy PI ortholog ThtPI, which results in complete loss of stamen identity and a full conversion to carpels upon down-regulation (LaRue et al., 2013). Loss of petaloid features was also partial in ThtPI knockdowns, consisting of green streaks on otherwise white sepals, suggesting partial redundancy of this function with other B-class genes, and likely also E-class genes (LaRue et al., 2013; Soza et al., 2016). Incomplete homeotic conversion of floral organs can be attributed to partial redundancy among the ThAP3 paralogs, supported by the presence of similar phenotypes in different treatments. This scenario differs from Aquilegia, in which the three AqAP3 paralogs have sub-functionalized to stamen or petal identity (petals are absent in Thalictrum and so is the petal-identity paralog AP3-3) and neo-functionalized to staminodia identity (a fifth type of organ not present in Thalictrum) (Sharma et al., 2011; Sharma and Kramer, 2013). Additional experiments using double and triple constructs to target multiple genes will be needed to fully dissect the degree of redundancy amongst the Thalictrum AP3 paralogs.
The up-regulation of all B-class genes in plants targeted for ThtAP3-2a silencing was unexpected and, barring a general issue with our VIGS experiments, we propose two (admittedly speculative) working hypotheses leading to testable predictions for future experiments. The truncated ThtAP3-2a protein could be acting as a dominant negative (Figure 6A), or there could be a unidirectional back-up circuit effect (Figure 6B). Under the dominant negative hypothesis, ThtAP3-2a is able to form protein dimers (Figure 4A), but unable to form tetramers. A dominant negative regulation may arise from mutations in ThtAP3-2a affecting hydrophobic residues in the K helices (Supplementary Figure S4) that are key to tetramerization (Puranik et al., 2014), or from the loss of the highly conserved C-terminal motifs (the paleo-AP3 region and PI motif-derived; Kramer et al., 1998). While domain-swap and rescue experiments in Arabidopsis, including a truncated Chloranthus AP3, have demonstrated that the C domain and its motifs do not affect protein function (Piwarzyk et al., 2007; Su et al., 2008), the ability for the ranunculid Eschscholzia californica PI ortholog SEIRENA to form tetramers is dependent on five conserved residues within the PI motif (Lange et al., 2013). One future direction to test whether ThtAP3-2a is acting as a dominant negative would be to overexpress it, with the prediction that it would result in a loss of B-function phenotype; unfortunately stable transformation protocols are currently not available for Thalictrum. Alternatively, back-up circuits have been proposed as a mechanism in paralog retention, where one paralog compensates for the decreased expression of a partner gene (Figure 4B; Kafri et al., 2005, 2006). The variable distribution of AP3 binding sites among the three ThtAP3 promoters (Figure 5F) lends support to this hypothesis, as paralogs with partially overlapping regulatory motifs are more efficient at rescuing the function of their mutated counterpart than paralogs with highly similar or highly dissimilar sets of motifs (Kafri et al., 2005). Likewise, the presence of more AP3 binding sites in the promoters of ThtAP3-1 and ThtAP3-2b supports the hypothesis that these genes are “backing-up” ThtAP3-2a. Both hypothetical models rely on an initial ThtAP3-2a down-regulation to trigger an increase in the positive regulation of all B-class genes. The back-up model presumably leads to a more immediate increase in expression of ThtAP3-1 and ThtAP3-2b, as there is also a primary “back-up” response of these paralogs (by an unknown mechanism, note different shape of gene expression curves in Figure 6A versus Figure 6B). Since we were unable to detect the putative transient down-regulation of ThtAP3-2a, a more comprehensive expression analysis would need to be done during earlier developmental stages to provide evidence for either of these arguments. Additional experiments are also needed to test identified binding sites in silico, and to ascertain whether divergent amino acids or lack of C-terminal motifs negatively affect ThtAP3-2a function.
FIGURE 6. Hypothetical models for B-class gene regulation in Thalictrum thalictroides. (A) Dominant Negative Model. ThtAP3-2a is presumably able to form protein dimers (K domain intact), either hetero-dimers (shown) or homo-dimers (not shown). These “non-functional” dimers are unable to form the tetramers needed to drive transcription, as required for positive auto- and cross-regulation. ThtAP3-1 and ThtAP3-2b form protein complexes that positively auto- and cross-regulate, driving transcription of the other B-class genes. After ThtAP3-2a is down-regulated, as a result of targeted gene silencing (red line in graphs), the higher ratio of functional to non-functional dimers creates an overabundance of tetramers, which drives the over-expression of all B-class genes (blue line). (B) Back-up Circuit Model. In response to the initial down-regulation of ThtAP3-2a (dotted red line in graphs) during targeted gene silencing, expression of ThtAP3-1 and ThtAP3-2b is up-regulated by a (as yet unknown) compensatory mechanism. Higher expression of ThtAP3-1 and ThtAP3-2b initiates an excess of positive auto and cross-regulation due to total protein levels, as opposed to protein ratios in the Dominant Negative Model (note different shapes of curves from panel A), causing an increase in the expression of all B-class genes (dotted blue line).
As a representative of an early diverging eudicot, Thalictrum is in a key phylogenetic position to study the evolution of floral MADS box protein–protein interactions. Our yeast two-hybrid assays showed novel and promiscuous interactions among the different Thalictrum AP3s. Core eudicot EuAP3 and most monocot paleoAP3 proteins do not homodimerize, but rather interact as obligate heterodimers with PI (Schwarz-Sommer et al., 1992; Tröbner et al., 1992; Riechmann et al., 1996; Moon et al., 1999; Vandenbussche et al., 2004), and this may have led to the canalization and increased robustness of the eudicot flower (Lenser et al., 2009; Melzer et al., 2014). However, AP3 and PI orthologs from early-diverging angiosperms and monocots are able to interact both as homo- and heterodimers (Melzer et al., 2014). AP3 homodimerization was probably lost very early in angiosperm evolution (before the eudicot–monocot split), while PI homodimerization was likely lost later, but before the diversification of the eudicots (Melzer et al., 2014). Evidence presented here suggests that Thalictrum floral MADS-box protein biochemical behavior more closely matches that of early diverging angiosperms than that of core eudicots. Aquilegia vulgaris AP3 (AqvAP3-2 and AqvAP3-3) have also been shown to homodimerize, yet the three proteins do not dimerize with each other (Kramer et al., 2007). All three Thalictrum AP3s not only heterodimerize with ThtPI as expected, but also homodimerize and heterodimerize with each other (Figure 4). In addition, all four B-class protein products can interact with the E-class partner ThtSEP3. While certain interactions only occurred in one direction, similar asymmetrical results have been observed, and deemed valid, in previous publications for other MADS box genes (e.g., Galimba et al., 2012; Lange et al., 2013). Yeast two-hybrid experiments provide evidence for biochemical interaction amongst the candidate proteins and are typically used as proxy; further studies will be needed to confirm whether these interactions occur in planta. Taken together, our results suggest that ThtAP3s can form homodimers, in addition to the AP3-PI heterodimers that preferentially populate B-class/E-class tetramers in Arabidopsis (Melzer and Theißen, 2009). Our detection of AP3 binding sites in the promoters of all B-class genes (Figure 5) supports auto- and cross-gene regulation, as has been described for MADS box genes more generally (Kaufmann et al., 2009). We therefore propose that these novel protein interactions provide a potential mechanism for the role of ThtAP3s in ectopic petaloidy of sepals.
Although gene duplication has long been recognized as an important contributor to the evolution of biological complexity (Ohno, 1970; Force et al., 1999), functional studies showing the fate of duplicated developmental genes are still limited. Here, we analyzed the function of duplicated AP3 orthologs from a basal eudicot and found deep conservation in stamen identity, a novel role in ectopic petaloidy and stigma development, and partial functional redundancy. While additional experiments will be needed to fully dissect the complex genetic interactions uncovered by our work, evidence presented here lends further support to the overarching hypothesis that the duplication of floral organ identity genes contributed to angiosperm diversification via the generation of floral diversity.
KG performed the experiments and wrote the manuscript. JM-G performed the yeast two-hybrid and promoter analysis and assisted with methods, descriptions, and supplementary materials. VDS designed the study, secured the funding, coordinated the experiments, and edited the manuscript.
This work was funded by NSF-IOS 1121669 to VDS. KG was supported by the National Institutes for Health Training Grant T32 EY07031. JM-G was supported by the Society for Developmental Biology Choose Development! Program (NSF-IOS 1239422) and University of Washington US Department of Education Ronald E. McNair Postbaccalaureate Achievement Program, GenOM Project (NIH-5R25HG007153-03) and Department of Biology’s Frye-Hotson-Rigg and UW Biology Scholarships.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
We thank the UW Biology Greenhouse staff for plant care and Dr. Edwige Moyroud for helpful conversations regarding motif analysis. This manuscript shares content only with KG’s doctoral dissertation (Galimba, 2015), and its publication is in accordance with the University of Washington’s dissertation publishing policies.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2018.00334/full#supplementary-material
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Keywords: ABC model, MADS-box genes, B-class genes, ectopic petaloidy, flower development, non-core eudicot, VIGS, Thalictrum thalictroides
Citation: Galimba KD, Martínez-Gómez J and Di Stilio VS (2018) Gene Duplication and Transference of Function in the paleoAP3 Lineage of Floral Organ Identity Genes. Front. Plant Sci. 9:334. doi: 10.3389/fpls.2018.00334
Received: 08 November 2017; Accepted: 28 February 2018;
Published: 23 March 2018.
Edited by:Elena M. Kramer, Harvard University, United States
Reviewed by:Pablo Daniel Jenik, Franklin & Marshall College, United States
Madelaine Elisabeth Bartlett, University of Massachusetts Amherst, United States
Copyright © 2018 Galimba, Martínez-Gómez and Di Stilio. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Verónica S. Di Stilio, email@example.com
†Present address: Kelsey D. Galimba, Appalachian Fruit Research Station, United States Department of Agriculture – Agricultural Research Service, Kearneysville, WV, United States