PpSAUR5 promotes plant growth by regulating lignin and hormone pathways

Introduction Peach (Prunus persica) has a high nutritional and economic value. However, its overgrowth can lead to yield loss. Regulating the growth of peach trees is challenging. The small auxin-up RNA (SAUR) gene family is the largest family of auxin-responsive genes, which play important roles in plant growth and development. However, members of this gene family are rarely reported in peach. Methods In this study, we measured leaf area, chlorophyll and lignin content to detect the role of PpSAUR5 on growth through transgenic Arabidopsis. Results PpSAUR5 responds to auxin and gibberellin, promoting and inhibiting the synthesis of gibberellin and auxin, respectively. The heterologous transformation of PpSAUR5 in Arabidopsis led to enhanced growth of leaves and siliques, lightening of leaf color, decrease in chlorophyll content, increase in lignin content, abnormalities in the floral organs, and distortion of the inflorescence axis. Transcriptome data analysis of PpSAUR5 overexpression and wild-type lines revealed 854 differentially expressed genes (DEGs). GO and KEGG analyses showed that the DEGs were primarily involved in biological processes, such as cellular processes, metabolic processes, response to stimuli, and catalytic activity. These genes were mainly enriched in pathways, such as phenylalanine biosynthesis, phytohormone signaling, and MAPK signaling. Discussion In summary, these results suggested that PpSAUR5 might regulate tree vigor by modulating the synthesis of auxin and gibberellin. Future studies can use PpSAUR5 as a candidate gene to elucidate the potential regulatory mechanisms underlying peach tree vigor.


Introduction
Peach (Prunus persica) is an important economic fruit tree with a wide cultivation area.However, the new shoots of peach trees grow vigorously.Improper management of peach trees might lead to excessive growth, leading to a burden on tree nutrition and, consequently, a decrease in yield.In orchard production, the vigor of peach tees is regulated by pruning or spraying the trees with growth regulators, which balances the vegetative growth and reproductive growth while increasing the production cost (Li et al., 2020).Therefore, it warrants the need to find novel, more cost-effective ways to efficiently manage peach tree growth.To date, a limited number of studies have focused on the regulatory mechanisms of peach vigor-related genes.
Phytohormones play crucial roles in regulating plant growth and development.Among them, auxin and gibberellin are essential for several developmental processes in plants, such as organ elongation (Tao et al., 2008;Sandalio et al., 2016); apical hook curvature growth and root hair development (Lee and Cho, 2013;Beźiat and Kleine-Vehn, 2018); response to temperature (Gray et al., 1998) and light signals (Stepanova et al., 2008); and seed germination, flowering induction, and pollen maturation (Achard and Genschik, 2009).Moreover, these hormones interact with each other too.Ross et al. (2000) showed that exogenous auxin treatment reduces bioactive gibberellin (GA 1 ) contents in pea stems.In Arabidopsis, fertilization-induced auxin activates GA biosynthesis; however, the application of exogenous GA does not affect auxin synthesis (Dorcey et al., 2009).SlDELLA, a GA signaling inhibitor, interacts with auxin signaling components SlIAA9 and SlARF7 to regulate tomato fruit development (Hu et al., 2018).
The SAUR family is an auxin-responsive, plant-specific, and extremely abundant gene family (Stortenbeker and Bemer, 2019).SAUR genes were originally identified in soybean hypocotyls and are extremely sensitive to exogenous auxin (McClure and Guilfoyle, 1987).Members of this gene family have been identified in several plants, such as Arabidopsis, tobacco, and maize (Newman et al., 1993;Gil et al., 1994;Knauss et al., 2003).Notably, SAUR genes have been found to exhibit similar functions across different plant species and primarily mediate cell elongation.For instance, SAUR53 promotes cell and organ elongation in Arabidopsis and modulates apical hook development; however, it is not induced by exogenous auxin (Kathare et al., 2018).Overexpression of the SAUR19-24 genes enhances cell expansion, increases hypocotyl length and leaf size, and alters overall plant growth (Xie et al., 2015).In maize and soybean, SAUR family genes are primarily expressed in elongated tissues, suggesting that these genes are involved in cell elongation.Another study reported that SAUR36 is significantly less expressed in young leaves than in old leaves, and saur36 mutant Arabidopsis plants exhibit a significant delay in leaf senescence, indicating the involvement of this gene in promoting leaf senescence (Hou et al., 2013).In a more recent study, treatment of SAUR10-clade transgenic Arabidopsis with different hormones showed that SAURs respond to auxin (indole-3-acetic acid, IAA), gibberellic acid (GA), abscisic acid (ABA), ethylene, and cytokinin (van Mourik et al., 2017).In rice, OsSAUR39 and OsSAUR45 have been shown to modulate plant growth by inhibiting auxin synthesis and transport (Kant et al., 2009;Xu et al., 2017).In addition, SAUR genes also respond to signals such as drought, low temperature, pests, and diseases.
Auxin activates plasma membrane (PM) H + -ATPase, mediating proton outflow.The hydrogen bonds in cell walls break under acidic conditions.In addition, an acidic environment changes the activity of cell wall-modified protein, leading to the degradation of the bond between xylan and cellulose microfibrils and cell wall relaxation (Xia et al., 2019).SAUR genes promote cell expansion by activating PM H + -ATPase via an acidic growth mechanism.Previous studies have shown that there is an antagonistic relationship between SAUR proteins and D-type protein phosphatase 2C (PP2C.D), a plant growth-related protein.For instance, the auxin-induced SAUR19 protein inhibits PP2C.D (D-type protein phosphatase 2C) activity (Spartz et al., 2017).pp2c.d2 and pp2c.d5derivatives have been shown to constitutively dephosphorylate and inhibit PM H + -ATPases, restricting plant cell elongation and organ growth (Wong et al., 2019).Our previous studies showed that PpSAUR5 expression is positively correlated with peach tree vigor.Therefore, PpSAUR5 could be considered as a candidate gene for regulating tree vigor in peach.In the present study, we constructed PpSAUR5overexpressing Arabidopsis plants using the Agrobacteriummediated method.Phenotype, organ length, and chlorophyll and lignin contents were determined in transgenic lines.Furthermore, the responses of the transgenic lines to different hormone treatments were studied, and transcriptome analysis was performed on wild-type and SAUR5-8 overexpression lines to determine the relationship between PpSAUR5 expression and the growth potential of peach trees.

Plant materials and growth conditions
Arabidopsis thaliana Col-0 was used for the transgenic assay.Arabidopsis seeds were disinfected and sown in Murashige and Skoog (MS) medium.When the seedlings had developed three to four leaves, the seedlings were transplanted to soil and placed in a climate incubator with a 16-h/8-h photoperiod at 23°C.
Nicotiana benthamiana was used for luciferase complementary assay.Seeds were sown in soil and placed in a climatic incubator with a 16-h/8-h photoperiod, humidity of 80% at 23°C.

Gene cloning and vector construction
Total RNA was extracted from the shoots of peach cultivar 'Jiuyan' using the RNAprep Pure Plant Kit (Tiangen Biotechnology, Beijing, China).Then, cDNA was synthesized using the TRUEscript RT Master Mix Kit (Adelaide Biotechnology, Beijing, China).Polymerase chain reaction (PCR) was performed using the cDNA as the template, and the reaction protocol was as follows: 98°C for 2 min; 33 cycles of 98°C for 10 s, 60°C for 15 s, 68°C for 30 s; 68°C for 10 min; and stored at 4°C.The PCR products were detected using 1% agarose gel electrophoresis, and the target bands were recovered using the Takara Gel Recovery Kit (TaKaRa Biotechnology, Dalian, China).The obtained DNA target fragment was ligated to the pEASY ® -Blunt Cloning Vector and sequenced to validate its accuracy.Then, the DNA target fragment was inserted into the expression vector pRI-101.The primers used are shown in Supplementary Table S1.

Quantitative real time-PCR
Quantitative real time-PCR (qRT-PCR) was performed using 2x AugeGreen qPCR Master Mix (US EVE-RBRIGHT® INC).The reaction mix included 10 mL of 2x Fast Super EvaGreen® Master Mix, 2 mL each of forward and reverse primers (10 mM each), 2 mL of cDNA, and 4 mL of ddH 2 O.The qRT-PCR protocol was as follows: 95°C for 60 s, followed by 45 cycles of 95°C for 10 s, 58°C for 10 s, and 72°C for 10 s.The dissolution curve program was as follows: 95°C for 10 s, 65°C for 60 s, and 97°C 10 s.Relative gene expression was calculated using the 2 −DDCT method.There were 10 genes randomly selected for qRT-PCR to verify the accuracy of transcriptome data.The internal reference gene was ubq5.The primers used are shown in Supplementary Table S2.

Yeast two-hybrid assay and luciferase complementary assay
The yeast two-hybrid (Y2H) expression vectors pBT3-STE and pPR3-N were used for the Y2H assay.The bait and prey plasmids were co-transformed into the yeast strain NMY51.Then, the strains were spread on SD/-Trp-Leu-deficient medium (DDO) and incubated at 28°C for 2-3 days.The clones were then spread onto SD/-Trp-Leu-Ade-His (QDO) and SD/-Trp-Leu-Ade-His + X-a-gal (QDO/X/A) media and incubated for 3-4 days to validate the interaction.
The expression vectors pCAMBIA1300-NLuc (pNL) and pCAMBIA1300-CLuc (pCL) were used for the luciferase complementation assay.From these vectors, recombinant plasmids pCAMBIA1300-PP2C.D2-NLuc and pCAMBIA1300-SAUR5-Cluc were constructed.The empty vector and the recombinant plasmid were transformed into Agrobacterium GV3101.PP2C.D2-Nluc + SAUR5-Cluc was the experimental group.PP2C.D2-Nluc + pCL, SAUR5-Cluc + pNL, and pNL + pCL were used as the control groups.Four-week-old vigorously growing Nicotiana benthamiana was selected as the material.10 mM 2-morpholinoethanesulfonic acid (MES), 10 mM MgCl 2 •6H 2 O, and 10 mM acetosyringone (AS) were mixed to prepare the resuspension.The OD value of resuspended bacteria was 0.6.The four groups of mixed bacterial solutions were injected into the abaxial surface of the Nicotiana benthamiana leaves in different areas, and the leaves were observed after 2-3 days of incubation.

Transgenic Arabidopsis assay
The expression vector pRI-PpSAUR5 was transformed into Agrobacterium GV3101 using the floral dip method (Clough and Bent, 1998).The seeds of T0 generation were sown in MS medium (supplemented with 50 mg/L kanamycin).After two resistance screenings, if all the seeds germinated and survived, they were considered pure overexpression lines.For subsequent analyses, T2 generation plant DNA was used as the experimental template, expression plasmid DNA was used as the positive control, and wildtype Arabidopsis thaliana DNA was used as the negative control.The upstream and downstream primers were designed for PCR detection.The upstream primer was GCTCCTACAAATGCCATCA, and the downstream primer was TTACCAAATTGTTTTATCTGAAAAT.

Assessment of phenotypic characteristics
Arabidopsis seeds were screened for two generations to obtain homozygous overexpression lines.Three overexpression lines, SAUR5-8, SAUR5-9, and SAUR5-15, with varying PpSAUR5 expression levels, were selected for further analyses.The hypocotyl length, root length, total chlorophyll content and levels of auxin and gibberellin in the lines were determined at 7 days after germination.The rosette leaf disc diameter and leaf area were measured at 20 days post-germination.Furthermore, we measured the length and number of stigmas and stamens at 45 days using an anatomical microscope (Zeiss Stereo Microscope Stemi 2000).

Analysis of PpSAUR5 response to phytohormones
Media with varying concentrations of exogenous hormones were prepared.Separate media were prepared containing 50 nM, 75 nM, and 100 nM IAA; 50 mM, 100 mM, and 150 mM GA; and 10 mM and 20 mM N-1-naphthylphthalamic acid (NPA).Wild-type and transgenic Arabidopsis seeds were sown in MS medium, and seeds with consistent germination were picked and placed vertically in hormone-supplemented media.The root length of 7-day Arabidopsis thaliana was measured.Root length inhibition rate (%) = [(control group-experimental group)/control group].

Determination of hormone levels
Endogenous hormone levels were determined in wild-type and transgenic Arabidopsis lines using high-performance liquid chromatography.Briefly, 1 g of plant sample (Arabidopsis at 7 days) was weighed and added to a mixture containing 8 mL of 80% methanol solution and the antioxidant butylated hydroxytoluene (BHT).The sample was ground, homogenized, and extracted for 12 h at 4°C in the dark.The mixture was then subjected to ultrasonic treatment for 1 h on ice and centrifuged at 12,000 rpm for 15 min at 4°C.The supernatant was transferred to a fresh centrifuge tube, and nitrogen was blown into the aqueous phase.The pH of the aqueous phase was adjusted to 8.0 with 1 mol/L Na 2 HPO 4 solution.Then, the sample was mixed with 0.2 g polyvinylpyrrolidone (PVPP), sonicated on ice for 0.5 h, and centrifuged at 12,000 rpm at 4°C for 5 min.The supernatant was transferred to a fresh centrifuge tube.The pH of the supernatant was adjusted to 3.0 with 1 mol/L citric acid.The extract was obtained with 3 mL ethyl acetate, ultrasonically shaken for 10 min, and then incubated in the dark for 1.5 h-2 h.The upper liquid layer was transferred to a fresh centrifuge tube and blown with nitrogen.When ethyl acetate was blown dry, 2 mL of 20% methanol was added to the residue for redissolution.An activated C18 column was rinsed with methanol and then with ultrapure water.The redissolved sample was transferred to a C18 column followed by 10% methanol rinse.Then, the column was again rinsed with 1 mL methanol at pH 8.0 and the liquid was collected into the injection bottle.

Determination of chlorophyll content
The 7-day Arabidopsis was ground into powder in liquid nitrogen and added to a mixture of acetone and anhydrous ethanol (2:1).After incubating at 4°C for 12 h, the solution was centrifuged at 4,000 rpm for 5 min at room temperature, and the absorbance values of the supernatant were measured at 645 nm and 663 nm.

Determination of lignin content
The lignin content in the plants was measured as described previously, with some modifications (Van Acker et al., 2013).The 20-day Arabidopsis was dried at 80°C to a constant weight, crushed, and passed through a 50-mesh sieve.Next, 5 mg of this sample was transferred to a 1.5-mL centrifuge tube.Then, 500 mL of 25% bromohexanoyl-acetic acid and 20 mL of 70% perchloric acid were added to the tube.The tube was then sealed with a sealing film, and the contents were fully mixed.The solution was then incubated in a water bath at 80°C for 40 min for sample acetylation.During the incubation, the sample was shaken every 10 min.After incubation in the water bath, the sample cooled naturally.Then, 500 mL of 2 M sodium hydroxide was added to the tube and mixed thoroughly.The tube was then left to stand.Finally, the absorbance value (A) of the sample was measured at 280 nm.The lignin content was measured using the following formula: Here, A assay and A blank are the absorbance values of the assay and the blank, respectively, and W is the sample mass.

Effects of PpSAUR5 overexpression on plant growth
The overexpression lines exhibited markedly enhanced plant growth, longer petioles, and lighter leaf color than Col-0 (Figure 1A, Supplementary Figure S1).Furthermore, the overexpression lines exhibited lower total chlorophyll content and significantly elongated hypocotyls and roots than Col-0 (Figures 1B-D).In addition, the transgenic lines exhibited significantly enhanced rosette leaf disc diameter and leaf area than wild-type plants.The largest leaf area measured in Col-0 was 36.98 mm 2 , whereas that measured in the overexpression lines was >50 mm 2 (Figures 1E, F).These findings indicated that PpSAUR5 overexpression modulated the vegetative growth of Arabidopsis.

Effects of PpSAUR5 overexpression on floral organs
All the overexpression lines exhibited significant elongated and curved flower stigmas, with the most pronounced changes in the pistil.The stigmas in these lines were 0.75 times longer, and the bending degree was seven times higher than in Col-0, but the stigma gradually straightened at the later stage of development (Figures 2A-C; Supplementary Figure S2).Furthermore, the transgenic lines exhibited fewer stamens (four to five) than Col-0 (six).The calyx of the overexpression lines was significantly elongated and did not close tightly.In addition, the petals in these lines appeared later than Col-0, and the stigma showed a curved shape inside the bract (Figures 2D, E).The inflorescence stems of the transgenic plants grew spirally at the fruiting stage, and the siliques were significantly elongated with rounded tips and larger apical diameters (Figure 2F).

Effects of PpSAUR5 overexpression on lignin content
Lignin is an important component of plants and is closely related to their growth.For instance, previous studies have shown a significant correlation between high lignin content and enhanced plant growth in alder (Li, 2001;Lv et al., 2018;Sun et al., 2019).In the present study, we observed that the Col-0 line had lower lignin content (29.27%) than the overexpression lines (44.80%, 51.59%, and 53.23%).Thus, PpSAUR5 overexpression led to a significant increase in the lignin content (Figure 3A).Even the lignin staining was more intense (dark red) in the overexpression lines, indicating higher lignin accumulation (Figure 3B).These findings indicated that PpSAUR5 might enhance overall plant growth by promoting lignin synthesis.

PpSAUR5 is responsive to auxin and gibberellin
Auxin and gibberellin play an important role in promoting plant growth.Previous studies have shown that SAUR5 family members respond to GA and IAA (Zhai et al., 2023).We assessed the response of Col-0 and PpSAUR5 transgenic lines to varying concentrations of IAA and GA.Our results showed that, compared with the Col-0, the overexpression lines showed significantly lower and higher inhibition after IAA and NPA treatment, respectively (Figures 4A, B).GA at 50 mM had no significant impact on transgenic lines; however, the inhibition rate increased remarkably after treatment with 100 mM and 150 mM GA (Figure 4C).After 7 days of treatment, the overexpression lines exhibited significantly higher and lower levels of auxin and gibberellin, respectively, than Col-0 plants.The differences in the GA and auxin levels were the largest between Col-0 and SAUR5-8 and Col-0 and SAUR5-15 lines, respectively (Figure 4D).Thus, these findings suggested that PpSAUR5 expression promotes gibberellin synthesis and inhibits auxin synthesis, indicating the involvement of this gene in auxin and gibberellin signal transduction.

Interaction between SAUR5 and PP2C.D2
PP2C.D protein is essential for plant growth and development, especially in organ growth and phototropism.It binds to SAUR proteins to negatively regulate cell expansion, thereby facilitating organ elongation (Ren et al., 2018).Thus, we hypothesized that PpSAUR5 also interacts with PP2C.D2.Y2H and luciferase complementation assays were used to validate this hypothesis.

Analysis of transcriptome data
Next, we performed transcriptome analyses of wild-type and SAUR5-8 lines to elucidate the role of PpSAUR5 overexpression in inducing multiple phenotypes.Our results showed a GC content of 45%~46%, with Q20 > 99% and Q30 > 94%.The clean reads of each sample were compared with the designated reference genome for sequence alignment and obtained an alignment efficiency of >96% (Table 1).This finding indicated that the sequencing quality was good and ready for follow-up analyses.We identified 854 differentially expressed genes (DEGs) between the wild-type and SAUR5-8 lines, with 753 genes upregulated and 101 genes downregulated in the overexpression line (Supplementary Table S3).Of these, the top 20 DEGs were selected for further analyses (Table 2).

Functional analysis of DEGs
The GO analysis classified the selected DEGs into three categories: biological processes, cellular components, and molecular functions (Figure 6A; Supplementary Table S4).Among the cellular components, the selected DEGs were highly enriched in cells, cell parts, cell membranes, and membrane parts.Among the biological processes, they frequently enriched in cellular processes, metabolic processes, and responses to stimuli.Among molecular functions, they frequently enriched in nucleic acid binding transcription factor activity, catalytic activity, and transporter activity.Furthermore, KEGG pathway analysis showed that the selected genes enriched in the plant hormone signal transduction, the phenylpropanoid biosynthesis, the MAPK signaling, and the plant-pathogen interaction pathways (Figure 6B; Supplementary Table S5).Based on the phenotype and hormonal response of transgenic plants, we next focused on the phenylpropanoid biosynthesis pathway, a hormone signal transduction pathway related to plant growth potential.

Discussion
Auxin is an essential phytohormone that regulates plant growth both directly and indirectly.The gibberellin signal transduction pathway comprises the DELLA protein, which inhibits the gibberellin response by binding to the sequestering transcription factor, similar to the auxin signaling pathway (Stamm and Kumar, 2013).The expression GA biosynthetic genes is regulated by Aux/ IAA and ADP ribosylation factor (Frigerio et al., 2006).Auxin regulates gibberellin-induced root growth by degrading the DELLA protein (Fu and Harberd, 2003).On the contrary, GA regulates the PIN-FORMED (PIN) protein, impacting the distribution of auxin in the root tip (Willige et al., 2011).In tomato, SlARF7 has been found to induce auxin and gibberellin responses during fruit development (de Jong et al., 2011).
The expression of the SAUR gene family members can be rapidly modulated by auxin treatment.It is one of the auxin response gene families.Eighty members of the SAUR gene family, including two pseudogenes, have been identified in Arabidopsis.However, only a few SAUR genes have been functionally characterized.A previous study reported AAM1, a member of the SAUR family, to be closely associated with apical hook development in Arabidopsis (Park et al., 2007).AtSAUR63 overexpression has been found to elevate auxin levels in Arabidopsis hypocotyls and promote hypocotyl and stamen filament elongation (Chae et al., 2012).SAUR41 overexpression has been found to result in hypocotyl elongation, distorted inflorescence stems, enlarged petals, and an increase in the number of lateral roots in Arabidopsis (Kong et al., 2013).Early leaf decay has been reported in plants overexpressing SAUR71 and SAUR72 (Zhou However, studies on the SAUR family members of peach have been rarely reported (Hagen and Guilfoyle, 2002;Ma et al., 2017;Guo et al., 2019).
Several studies have shown that the biological clock regulates auxin signal transduction and the expressions of many auxininduced genes, resulting in varying plant sensitivity to auxin at different times of the day.The asymmetry in auxin accumulation is related to stem bending growth (Covington and Harmer, 2007;Chae et al., 2012).However, whether the distortion of the inflorescence stem observed in the overexpression lines in the current study is related to the circadian clock signal or the optical signal still remains to be investigated.
MeSAUR1 is highly expressed in cassava roots.Its expression increases after induction by IAA, gibberellin, and ethylene (Ma et al., 2017).AtSAUR36 is induced by auxin but inhibited by gibberellin.Its expression can also be affected by polyphenols and exogenous ABA treatment (Stamm and Kumar, 2013).PIL1 (AT2G46970) interacts with COP1 to regulate the circadian rhythm, photomorphogenesis, and hypocotyl elongation (Luo et al., 2014).In the current study, the results of the transcriptome analysis showed that PpSAUR5 upregulated PIL1, which is involved in the gibberellin synthesis pathway (Figure 8B).In addition, PpSAUR5 was found to be responsive to auxin and gibberellin, as evident by increased gibberellin levels and decreased auxin levels in the overexpression plants (Figure 4).These results indicated that PpSAUR5 is involved in auxin and gibberellin signal transduction pathways.Jiang (2022) found significant pistil elongation in the PpIDD11 overexpression lines.Another study reported that AtSAUR63 promotes stamen filament elongation (Chae et al., 2012).However, to the best of our knowledge, there are no reports on the impact of SAUR family members on the number of stamens.In the current study, we found that PpSAUR5 overexpression led to a decrease in the number of stamens and elongation and bending of pistil stigmas (Figure 2).We also observed a significant increase in the diameter and leaf area of rosette leaf discs in the overexpression lines (Figures 1E, F).In addition, PpSAUR5 promoted the expansion of floral organs and the distortion of inflorescence stems during flowering (Figure 2), which was consistent with the phenotype of the plants overexpressing SAUR41 (Kong et al., 2013).The PP2C.D (Dtype protein phosphatase 2C) family is essential for plant growth and development processes, such as organ growth.SAUR has previously been found to activate PM H + -ATPase and promote cell expansion by inhibiting PP2C.D (D-type protein phosphatase 2C) activity (Spartz et al., 2017).In a previous study, overexpression of GFP-SAUR19 was found to inhibit the growth defects induced by PP2C.D5 (Ren et al., 2018).In line with these studies, in the present study, we found that SAUR5 interacted with PP2C.D2 (Figure 5), indicating that PpSAUR5 might impact shoot growth in peach by modulating PP2C.D2 activity.
We identified a total of 854 DEGs from the transcriptome data of overexpression and wild-type lines.These DEGs were found to play regulatory roles in chlorophyll synthesis, auxin and gibberellin signaling, and lignin synthesis.There were 40 DEGs were found to be associated with the phenylalanine metabolic pathway (Figure 7; Supplementary Table S6).In addition, we found higher lignin content and lower chlorophyll content in the overexpression lines than in the Col-0 lines, suggesting the potential involvement of PpSAUR5 in lignification and chlorophyll accumulation.Expression of phenylalanine pathway-related genes.

B A
Expression of auxin (A) and gibberellin (B) related genes.
Taken together, PpSAUR5 might promote plant growth by modulating the auxin and gibberellin signal transduction pathways.However, the process of plant growth and development is complex, and the specific regulatory mechanisms underlying PpSAUR5 action still need to be investigated.
FIGURE 2 Phenotypic observation of flower organs of Col-0 and PpSAUR5-overexpressing Arabidopsis at 45 days.Each data point represents mean of the data set, and bars represent standard deviation (n = 20).Letters indicate significant differences by t test (P = 0.05).(A) Phenotypic observation of pistil one day after flowering.(B) Bending angles of pistils.(C) Pistil stigma length.(D) Number of stamens.(E) Phenotypic observation of stamens and buds.(F) Phenotypic observation of inflorescence stems and pods.
FIGURE 4 Exogenous hormone treatment and endogenous hormone changes.In (A-C), the inhibition rate was root length inhibition rate.Root length inhibition rate (%) = [(control group-experimental group)/control group].In (E-G), from left to right is Col-0, SAUR5-8, SAUR5-9, and SAUR5-15.Letters indicate significant differences by t test (P = 0.05).(A) The root inhibition rate of Col-0 and PpSAUR5 Arabidopsis-overexpressing lines after IAA treatment for 7 days.(B) The root inhibition rate of Col-0 and PpSAUR5 Arabidopsis-overexpressing lines after NPA treatment for 7 days.(C) The root inhibition rate of Col-0 and PpSAUR5 Arabidopsis-overexpressing lines after GA treatment for 7 days.(D) Detection of auxin and gibberellin content in 7-day Col-0 and PpSAUR5 overexpressing Arabidopsis.(E) Growth of Col-0 and PpSAUR5 Arabidopsis overexpression lines treated with IAA for 7 d.(F) Growth of Col-0 and PpSAUR5 Arabidopsis overexpression lines treated with GA for 7 days.(G) Growth of Col-0 and PpSAUR5 Arabidopsis overexpression lines treated with NPA for 7 days.

Functional
analysis of DEGs in wild-type and PpSAUR5-8-overexpressing Arabidopsis.(A) GO functional categories of common DEGs.(B) The KEGG pathway of common DEGs.

TABLE 1
RNA-seq data of wild-type and PpSAUR5-overexpressing Arabidopsis.

TABLE 2
Information description of common differential genes.