OsWDRP3, a WD-40 repeat protein interacts with OsBAK1 to control leaf angle by modulating BR signaling

Leaf angle is an essential component of plant architecture. Brassinosteroids (BRs) plays important roles in regulating leaf angle. WD-40 repeat proteins (WDRPs) act as versatile scaffolds for protein–protein interactions and participate in plant growth and development. To date, the functions of OsWDRPs have been largely unknown. Here, we found that OsWDRP3 regulates leaf angle through the BR pathway in rice. qRT–PCR and GUS reporter assays revealed that OsWDRP3 was expressed in a variety of tissues, especially leaves. OsWDRP3 predominantly resides in the cytoplasm and aggregates near the cell membrane. OsWDRP3-RNAi plants exhibited less sensitivity to BR than the wild type. Using bimolecular uorescence complementation assays and Co-IP, we determined that OsWDRP3 interacts physically with OsBAK1. More importantly, an in vitro cell-free degradation assay showed that OsWDRP3 participates in the protein degradation of OsBAK1. We also found that the degradation of OsBAK1 was delayed in OsWDRP3 RNAi plants. In conclusion, our data suggest that OsWDRP3 affects BR signaling by regulating the concentration of OsBAK1 in the cytoplasm and thus regulating the leaf angle in rice.

physically interacts with OsBZR1 and then regulates leaf angle in rice (Qiao et al. 2017;Hirano et al. 2017). Some bHLH transcription factors, such as OsBLR1, participate in leaf angle regulation though the BR pathway in rice (Wang et al. 2020). Similarly, gain-of-function OsbHLH079 also causes a wide leaf angle, while OsbHLH079-RNAi lines show the opposite phenotype (Seo et al. 2020). OsBUL1 positively affects leaf angles by controlling cell elongation (Jang et al. 2017). Recently, Guo et al. (2021) demonstrated that OsbHLH98 negatively regulates leaf angle by regulating the transcription of OsBUL1. Therefore, BR biosynthesis and signaling greatly in uence the rice leaf angle.
WD40 repeat proteins have an approximately 40 amino acid core region. The N-terminus of the core region contains a glycine-histidine (GH) dipeptide, and the C-terminus has a tryptophan-aspartate (WD) dipeptide (Migliori et  ). ULCS1, a WD40 protein in Arabidopsis, participates in the degradation of various proteins by interacting with the E3 ligase complex (Beris et al. 2016). Another Arabidopsis WD40 protein, i.e., NEDD, plays a role in microtubule organization (Zeng et al. 2009). The WD repeat-containing protein TTG1 has functions in the immune response (Zhao et al. 2008). Therefore, studying the function of WD40 proteins is of great signi cance for further understanding the regulatory mechanism of plant development.
To date, there are approximately 200 putative WD40 proteins in rice (Ouyang et al. 2012). However, the roles of most WD40 proteins remain unknown. In this paper, we found that a WD40 protein in rice was involved in the regulation of leaf upright growth, and RNAi transgenic plants showed BR insensitivity. In vitro degradation results showed that the degradation of OsBAK1 was delayed in RNAi transgenic plants, which inhibited BR signal transduction. This study provides insights into the roles of OsWDRP3 in the BR pathway.

OsWDRP3-RNAi knockdown transgenic plants display erect leaves
To investigate the biological function of OsWDRP3, an OsWDRP3 mutant (wdrp3, 2A-20340) was isolated from a T-DNA insertion library with the cv Dongjin background (Jeon et al. 2000;Jeong et al. 2006). wdrp3 plants were short with a small leaf angle, but the number of seeds was very small; thus, we developed OsWDRP3-overexpressing and OsWDRP3-silenced lines to characterize the roles of OsWDRP3 in rice plants. Over 20 independent T0 OsWDRP3 RNAi lines were obtained. We then selected the RNAi14 line with the lowest OsWDRP3 gene expression to analyze the gene functions (Fig. 1A). We also generated transgenic rice plants overexpressing OsWDRP3 (OE) under the control of a maize ubiquitin promoter. The expression level of OsWDRP3 was higher in OE line 9 than in wild-type plants. We selected OE line 9 to analyze the phenotype (Fig. 1B). In this study, all the transgenic lines, including the OE and RNAi lines, were in the background of Hejiang19, a japonica variety.
OsWDRP3-RNAi lines showed a reduction in plant height (to 70%-75% of the wild-type height, n = 15, P < 0.01). OsWDRP3-OE plants were slightly higher than the wild ones, but there was no signi cant difference (Fig. 1C). Internode elongation was inhibited in all of the RNAi plants. We measured the lengths of the individual internodes of plants. The results showed that each internode of OsWDRP3-RNAi plants had a different length than the wild type. The rst, second, third and fourth internodes were shortened by 17%, 41%, 48% and 53%, respectively (Fig. 1D). Based on the proportion of each internode to the total internode length, OsWDRP3-RNAi plants belong to type D6 dwar sm, which is usually related to BR synthesis or signal transduction correlation (Takeda 1974). Additionally, although the plant height of the overexpressed transgenic plants was similar to that of the wild type, its internode length changed, in which the rst internode extended relative to the wild type. It was 39% longer in the rst internode, 2% shorter in the second, 43% shorter in the third and 88% shorter in the fourth compared with the wild type. Some overexpressed transgenic plants did not even have the fourth internode.
In wild-type rice, the leaf blade bends away from the vertical axis of the leaf sheath, whereas the leaves of OsWDRP3-RNAi seedlings were erect at the seedling and adult stages (Fig. 1). The second lamina joint angle of 9-day-old wild-type seedlings was 17.49 ± 4.09°, whereas that of the OsWDRP3-RNAi was 5.80 ± 1.63° (Fig. 1E), representing a 3-fold increase in the lamina angles of wild-type relative to that of the OsWDRP3-RNAi plants. At the heading and harvest stages, the ag leaf angle, second leaf angle and third leaf angle of OsWDRP3-RNAi plants were reduced by 36%, 28% and 32%, respectively, compared with the wild type (Fig. 1F). Since BR regulates the bending of the lamina joint (Yamamuro et al. 2000;Hong et al. 2003), these results suggest that OsWDRP3 may be involved in BR biosynthesis or signal transduction in rice.

OsWDRP3 participates in the regulation of BR synthesis and transduction
We checked the expression of OsWDRP3 in wild-type rice under BR treatment by quantitative PCR. Seven DAG wild-type rice seedlings were treated with 1 μM 24-epibrassinolide (24-eBL, the active BL), and leaves treated with 0 h, 2 h, 4 h, 8 h, 12 h and 24 h were extracted. Total RNA was extracted, and cDNA was synthesized by reverse transcription in vitro. OsWDRP3 gene expression increased after 2 h of treatment with 1 μM 24-eBL and decreased after 4 h of treatment ( Fig. 2A). The results showed that BR induced OsWDRP3 gene expression, suggesting that the OsWDRP3 gene may be involved in the BR signaling pathway. BR biosynthesis and signal transduction are modulated in an intricate manner in plants (Tanaka 2005). OsBRI1 and OsBZR1 have been identi ed, and their loss-of-function mutants display erect leaves (Yamamuro et al. 2000;Bai et al. 2007). OsBZR1 directly regulates the expression of the DWARF AND LOW TILLERING (DLT) gene, an important BR response factor in rice (Tong et al. 2009). To investigate whether OsWDRP3 was involved in the BR signaling pathway, we examined the expression of BR-related genes in wild type and OsWDRP3-RNAi. The expression of OsBRI1 was downregulated in wild-type plants under BR treatment, which was consistent with a previous report (Yamamuro et al. 2000). In RNAi transgenic plants, the expression of OsBRI1 was downregulated, and there was little change in the expression level after BR treatment. The results also showed that the BR signaling pathway regulation gene OsBAK1 upregulated expression in wild-type plants under BR treatment. Additionally, the expression of OsBAK1 was upregulated in RNAi plants but decreased after BR treatment, which was different from wild-type plants. The expression levels of BZR1, which plays positive roles in BR signaling, were upregulated when BR treatment was applied to wild-type plants, but no signi cant change occurred in OsWDRP3-RNAi plants (Fig. 2B).
We therefore analyzed the expression of BR biosynthetic genes in WT and OsWDRP3-RNAi (Tanabe et al. 2005;Hong et al. 2003). It was previously shown that the expression of CPD, which is involved in BR biosynthesis, is downregulated by BL treatment (Tanaka et al. 2005). Hence, the expression level of CPD can be used as an indicator of BL perception. We studied the effect of eBL on the expression of BRspeci c biosynthetic genes in wild-type and OsWDRP3-RNAi plants. When the plants were treated with eBL, the expression of these genes in the wild-type plants was visibly reduced but not affected in OsWDRP3-RNAi plants (Fig. 2C).
qRT-PCR results suggested that BR signal transduction was impaired in the OsWDRP3-RNAi plants. BR signaling represses BR synthesis in a negative feedback manner, and impaired BR signaling usually promotes the transcript accumulation of BR biosynthesis genes (Bai et al. 2007;Tong et al. 2009). These results suggest that OsWDRP3 might be a positive regulator in the BR signaling pathway.

OsWDRP3-RNAi plants show BR-insensitive phenotypes
To examine whether the leaf-bending morphology of OsWDRP3-RNAi was related to BR signaling, we tested the effect of exogenous BR on wild-type plants and RNAi plants.
First, we examined the coleoptile elongation of wild-type and OsWDRP3-RNAi seedlings in response to eBL. Rice seeds were germinated in MS medium in the dark with or without 1 μM eBL. In wild-type plants, coleoptile elongation was promoted when 1 μM eBL was added to the medium, but the same experimental phenomenon was not seen in OsWDRP3-RNAi plants (Fig. 3A).
Second, we tested the response of root growth of the wild-type and OsWDRP3-RNAi seedlings to eBL. In the absence of eBL, the root growth of OsWDRP3-RNAi plants was obviously shorter than that of the wild type. (Fig. 3 B). In the presence of 1 μM eBL, root elongation in wild-type seedlings was inhibited, whereas OsWDRP3-RNAi showed the same growth status before and after treatment (Fig. 3B). eBL can promote bending at the lamina joint, and BR-de cient and BR-insensitive mutants show decreased bending of the lamina joint (Cao and Chen 1995;Tanabe et al. 2005). We analyzed the sensitivity of OsWDRP3-RNAi and OsWDRP3-OE to eBL with a lamina joint assay (Yamamuro et al. 2000). The lamina inclination assay revealed that the OsWDRP3-RNAi plants displayed an insensitive phenotype to BR. After treatment with 100 nM 24-eBL, the second lamina joint angle of the 7-day-old wildtype and OsWDRP3-RNAi seedlings increased by 8.12 ± 0.18 and 4.83 ± 0.14 times, respectively (Fig. 3C).
The lamina angles of wild-type plants increased signi cantly after eBL treatment, whereas those of OsWDRP3-RNAi had no obvious response. There was no signi cant difference between OsWDRP3-OE and wild-type plants (Fig. 3C).
These results suggested that the OsWDRP3-RNAi seedlings were less sensitive to exogenous BR than wild-type seedlings.

OsWDRP3 is a WD40 repeat protein and widely express in rice
The deduced amino acid sequence of OsWDRP3 consists of 345 residues. The primary sequence contains seven WD40 domains, one WDxR motif and one putative DWD box (Fig. 4A). WD40 domains often fold into the most ideal and stable seven-bladed β-propellers with a funnel-like shape (Jain and Pandey 2018). We analyzed the WD40 domain in OsWDRP3 (https://swissmodel.expasy.org/). There were seven WD40 repeat domains and a funnel-like shape, as displayed in Figure 1A. This result suggests that OsWDRP3 may be involved in intracellular protein interactions similar to other WD40 proteins.
Comparison of amino acid sequences indicated that OsWDRP3 shared high identities with three WD repeat proteins in Arabidopsis (At3g15610, 79% sequence identity; At1g52730, 79% sequence identity; At1g15470/XIW1, 74% sequence identity) (Fig. 4B). These data clearly suggested that OsWDRP3 is one of the closest relatives of WD repeat proteins in Arabidopsis.
We performed RT-qPCR assays using total RNA from various tissues of plants at the seedling stage and reproductive stage, including panicles, different internodes, nodes, leaf blades, leaf sheaths, and roots.
OsWDRP3 expression was detected in all tissues examined but primarily in dividing tissues, including the uppermost internode, node, and leaf sheath. The abundance of transcripts encoding OsWDRP3 was highest in the internode at 60 days after germination (DAG) and lower in the seedling, stem and lamina joints of the japonica rice variety Hejiang19 (Fig. 5A).
To analyze the expression pattern of OsWDRP3 in detail, we cloned a 2-kb promoter region of OsWDRP3 to drive the GUS gene and then transformed rice plants. GUS staining was observed in various organs in transgenic plants. Overall, the histochemical staining results showed that OsWDRP3 expressed in most tissues throughout plant growth and development. A high level of expression was primarily observed in the root, pollen and internodes (Fig. 5B). We examined the lamina joint region, leaf blade and sheath in 9d-old transgenic seedlings (Fig. 5B). The veins in the leaf blade and sheath were well stained (Fig. 5B). In the reproductive stage, staining was observed in the vascular bundles of the lemma and palea in particular (Fig. 5B), and the anther was also stained (Fig. 5B). Thus, OsWDRP3 functions throughout plant growth and development.
To investigate the subcellular localization of OsWDRP3, we constructed a pUbi::OsWDRP3-GFP construct. We observed the uorescence of the OsWDRP3-GFP fusion protein and found that GFP was distributed in the cytoplasm (Fig. 5C), indicating cytoplasmic localization of OsWDRP3.
OsWDRP3 interacts with OsBAK1 and regulates its degradation in rice Based on the bioinformatics analysis, OsWDRP3 is a serine-threonine kinase receptor-associated protein.
Combined with the previous phenotypic analysis results, we speculated that OsWDRP3 might interact with BR-related serine-threonine kinases.
Brassinosteroid insensitive 1 (BRI1) is the BR receptor in plants. BRI1 heteromerizes with BRI1-associated kinase 1 (BAK1) and forms a receptor complex to activate BR signaling. We chose OsBRI1 and OsBAK1 to analyze the interactions with OsWDRP3.
OsBAK1-GFP fusion protein is principally located on the plasma membrane. However, OsBAK1-GFP was abundant in the cytoplasm during plasmolysis experiments and distributed in a spot-like way ). This result suggested that BAK1 might break off above the membrane and enter the cytoplasm under treatment conditions. Our BiFC results showed that OsBAK1 was also localized in the cytoplasm when it interacted with OsWDRP3 in rice protoplasts (Fig. 6B).
Coimmunoprecipitation assays showed that OsWDRP3 interacts with OsBAK1 in planta. Rice seedling leaves isolated from the Ubi::OsWDRP3-Myc transgene plant were ground in protein extraction buffer. After centrifugation, the supernatant was used as a total protein extract. Protein extracts (input) were immunoprecipitated with anti-MYC magnetic beads. Immunoblots were developed with anti-BAK1 antibody to detect BAK1 and with anti-MYC to detect OsWDRP3 (Fig. 6C).
We used in vitro degradation experiments to investigate whether OsWDRP3 promotes the degradation of the OsBAK1 protein. Puri ed OsBAK1-6His was incubated with protein extracts from wild-type, OsWDRP3-RNAi, and OsWDRP3-OE plants and detected with anti-6 × His, anti-OsBAK1, and antiplant actin antibodies. As shown in Figure 7, when the puri ed OsBAK1 259-624 and OsBAK1 307-624 proteins were incubated with the wild-type protein extract, only OsBAK1 259-624 proteins were degraded, while OsBAK1 307-624 proteins were not degraded (Fig. 7A). Subsequently, we examined the effect of OsWDRP3 on the degradation of OsBAK1 259-624 protein. OsBAK1 259-624 protein was incubated with protein extracts from OsWDRP3-OE, wild-type and OsWDRP3-RNAi plants, and the degradation rate of OsBAK1 259-624 protein was slowed down in turn (Fig. 7B).
To verify the effect of OsWDRP3 on the degradation of OsBAK1 259-624 protein, we added puri ed OsWDRP3 into the protein extract of wild-type plants and then incubated OsBAK1 259-624 protein. The degradation rate of OsBAK1 259-624 protein in the reaction system with OsWDRP3 added was faster than that in the system without OsWDRP3 added ( Fig. 7B and 7C).

Discussion
The WD provides a platform for protein interactions to form multiprotein complexes, which regulate In this paper, we found that OsWDRP3, as a WD40 protein in rice, is involved in the regulation of upright leaf growth. Based on the characterization of WD proteins, we analyzed the interacting proteins of OsWDRP3 to reveal the functions of OsWDRP3 in regulating leaf upright growth, and because OsWDRP3-RNAi transgenic plants showed BR insensitivity and semidwar sm, we chose those proteins that are related to BR signaling in rice.
Among these BR-related proteins, BRI1-associated kinase 1 (BAK1) was proven to interact with OsWDRP3. BAK1 is a Thr/Ser/Tyr kinase with ve leucine-rich repeat (LRR) copies. As a coreceptor, BAK1 mediates multiple signaling pathways, including BR signaling and PAMP-triggered immunity (He et al. 2013). Fine-tuning of BAK1 is essential to its function. Several proteins are involved in the regulation of BAK1. For example, BAK1-interacting receptor-like kinases3 (BIR3) can interact with BAK1 to prevent BAK1 receptor complex formation, thus negatively regulating BR signaling (Imkampe et al. 2017). MSBP1 (a membrane steroid-binding protein 1) can bind to BAK1 in vitro and is negatively involved in BR signaling (Song et al. 2009). Overexpression of a truncated intracellular domain of OsBAK1 (without the extracellular domain) results in BR insensitivity and a dwarfed phenotype ). These results indicate that the increase in BAK1 content in the cytoplasm can inhibit BR signal transduction.
Posttranslational regulation takes part in BR signaling. BES1 and BZR1 can be degraded by the proteasome He et al. 2002). Whether BAK1 is regulated by protein degradation has not been reported. Through bioinformatics analysis, we identi ed the homologous genes of the OsWDRP3 gene in Arabidopsis as At1g15470/XIW1, At3g15610 and At1g52730 ). Among them, XIW1 is XPO1-interacting WD40 protein 1 and interacts with ABA insensitive 5 (ABI5) in the nucleus and is involved in regulating the stability of ABI5 (Xu et al. 2019; Cai et al. 2020). Our previous work in Arabidopsis thaliana showed that a WD protein is involved in the degradation of the protein kinase CRK5 (Teng et al. 2016). OsWDRP3 is a serine-threonine kinase receptor-associated protein. Based on our results, we speculated that OsWDRP3 might interact with the BR-related serine-threonine kinase BAK1 and be involved in the intracellular degradation of BAK1 (Fig. 8). OsBAK1-GFP fusion protein is principally located on the plasma membrane. However, OsBAK1-GFP is abundant in the cytoplasm during plasmolysis experiments and distributes in a spot-like way ). This result suggested that BAK1 might break off above the membrane and enter the cytoplasm under treatment conditions. After BAK1 departs from the membrane and enters the cytoplasm through endocytosis, BAK1 might be degraded mediated by WDRP3 in the cytoplasm. It has been reported that overexpressed BAK1K in the cytoplasm inhibits BR signal transduction, leading to a BR-insensitive and dwarfed phenotype ). BAK1K in the cytoplasm can also bind to BRI1, but unlike BAK1 localized to the cell membrane, BAK1K in the cytoplasm cannot act as a coreceptor in BR signal transduction. Therefore, excess BAK1K in the cytoplasm can inhibit BR signaling to some extent (Fig. 8). In our future research, we will further try to reveal how WDRP3 participates in degradation in the cytoplasm in rice.
In summary, we showed the involvement of OsWDRP3 in BR signaling in rice, and the ndings implied that OsWDRP3 might be a potential genetic module for future rice breeding strategies.

Plant materials and growth conditions
The RNAi and OE lines were generated on the Hejiang 19 background. All rice plants were grown in paddy elds from May to September in Wuhan (104.06°E, 30.67°N), China. In winter, the plants were grown in green house with 16 h light and 8 h dark.
Dry rice seeds were immersed in NaClO solution (2% active chlorine) for 30 min, and then sterilized distilled water was used to wash away the remaining NaClO. The sterilized seeds were dried and then transferred to MS solid medium (SIGMA-ALDRICH). After grown for 7-10 days at 28°C with 16 h light and 8 h dark, the seedlings were transplanted to soil.

Sequence analysis
The OsWDRP3-related sequences from Arabidopsis were identi ed using Protein BLAST (https://blast.ncbi.nlm.nih.gov/Blast.cgi). Protein sequences were aligned using Jotun Hein Method.

Vector construction and rice transformation
To generate the RNAi construct (Ubi:RNAi-OsWDRP3), the region containing 539 bp of the OsWDRP3 coding sequence was ampli ed from Hejiang 19 cDNA and then transferred into the plant binary RNAi vector pUbi (modi ed from pCambia1301). The hairpin structure with two inverted repeat fragments was expressed under the control of the maize ubiquitin promoter.
To generate the over-express construct (Ubi::OsWDRP3), the full-coding region of OsWDRP3 was ampli ed from Hejiang 19 cDNA and inserted into pCambia1300-3×Flag.
The expression of OsWDRP3 in the wild type, OsWDRP3-RNAi and OsWDRP3-OE plants were examined by qRT-PCR.

RNA isolation and RT-PCR analyses
Total RNA was isolated from seedlings using the plant RNA puri cation reagent (Invitrogen). Transcript levels were detected by qRT-PCR. DNase (Fermentas) -treated total RNA (1 μg) were used to generate cDNA templates by Revert M-MuLV reverse transcriptase (Fermentas). qRT-PCR reactions were performed with denaturation 95°C for 5 min, 30 cycles of 95°C for 10 s, 60°C for 60 s and 72°C for 60 s. qRT-PCR was conducted using Biolab real-time PCR with SYBR Green Premix Ex TaqII (Takara, https://www.takarabio.com) according to the manufacturer's instructions. Data were analyzed using CFX manager software (Bio-Rad; www.bio-rad.com). For each gene, three replicates were analyzed. Each analysis was biologically repeated twice. OsUBQ10 was used to normalize the qRT-PCR data.

Histochemical GUS analysis
To obtain pOsWDRP3::GUS transgenic plants, a 3630 bp promoter region of OsWDRP3 was ampli ed using the forward primer 5′-CCCAAGCTTGAAGACATGGCAATTTGGT-3′ and the reverse primer 5′-CCCAAGCTTTGCATCAATCTCAACCCC-3′ from the genome of Hejiang19, and inserted into the Hind III site of the pCAMBIA-1381Xb-GUS vector.
Fresh samples from pOsWDRP3::GUS transgenic plants were incubated in a GUS staining solution at 37°C for 24 h. The GUS staining solution includes50 mM phosphate buffer (pH 7.2), 0.5% (v/v) Triton-X100, 5 mM potassium ferricyanide, 5 mM potassium ferrocyanide and 2 mM 5-bromo-4-chloro-3-indolyl-β-D glucuronide. Then the samples were treated with fresh 70% ethanol until no chlorophyll color left. In the end, we used microscope (DM1000; Leica, Wetzlar, Germany) to examine the samples and photographed with a digital camera.

Rice Protoplast Transformation
The wild-type rice seeds were placed on MS solid medium to grow for 8-10 days. The shoots of seedling were cut into 0.5-mm strips, and then incubated in enzyme solution with gentle shaking (50 rpm) at 28 °C for 4-5 h in the dark. The enzyme solution includes 0.6 M mannitol, 10 mM MES, 1.5% cellulase RS, 0.75% macerozyme R-10, 1 mM CaCl 2 , 0.1% BSA, 5 mM β-mercaptoethanol, pH 5.7. 10 mL of pre-cooled W5 solution (154 mM NaCl, 125 mM CaCl 2 , 5 mM KCl, 2 mM MES, pH 5.7) was slowly added to the enzymatic hydrolysate. Then the solution was ltered through a 35 mm nylon mesh. The protoplasts were collected by centrifugation at 1500 r/min for 3 min. The supernatant was sucked out with pipetting gun, then 2 mL of precooled MMG solution (0.6 M mannitol, 15 mM MgCl2, 4 mM MES, pH 5.7) was gently added to the protoplast, and then added 8 mL precooled MMG solution was mixed and ice bathed for 30 min to restore the vitality of protoplasts. The solution was centrifuged at 1500 r/min for 3 min, and then discarded the supernatant. The protoplasts were gently resuspended to a density of 2×10 6 / mL with MMG solution. Next, plasmid was mix with 100 μL of resuspended protoplasts, and then 110 μL of polyethylene glycol (PEG) solution (0.6 M mannitol, 100 mM CaCl 2 , 40% [w/v] PEG 3350) were added evenly. The mixture was incubated at 28 °C for 20 min. After centrifugation at 1500 r/min for 3 min, the protoplasts were resuspended in W5 solution with proper volume, and then incubated overnight at 28 °C in the dark.

Subcellular localization of the OsWDRP3 protein
To determine the subcellular localization of the OsWDRP3 protein, the full-length ORF of OsWDRP3 was cloned into the pmGFP4 vector, driven by the CaMV 35S promoter. The fusion construct was transferred into rice protoplasts, and the empty pmGFP4 as a control. This plasmid was introduced into the rice protoplasts through polyethylene glycol-mediated transformation Lichocka and Schmelzer, 2014). The subcellular localizations of OsWDRP-mGFP were observed using a laser scanning confocal microscope at the proper time after transformation or in ltration (Leica DMI6000 equipped with a Leica TCS SP8 confocal laser-scanning device, Leica Microsystems).

Brassinosteroid sensitivity assay
For lamina joint inclination analysis, after sterilization, the seeds were cultured in MS solid medium at 28°C until two-leaf stage. 1 μL of ethanol solution containing various concentrations (0, 10, 100, 1000 ng/ μL) of 24-epiBL were dropped at the lamina joints of the second leaf. After cultured for 2 days, the angles of the second leaf were photographed and measured with IMAGEJ. For each treatment, 10 plants were used to measure the angle. All the experiments were repeated three times For coleoptile elongation analysis, seeds were germinated in MS solid medium with or without 1 μM eBL at 28 ℃ in darkness for 3 days.
For root elongation analysis, seeds were soaked in water for 2 days at 28 ℃. Geminated rice seeds were then transferred to MS liquid medium with or without 1 μM eBL at 28 °C for 5 days.

Immunoblots
One-week-old seedlings were soaked in liquid nitrogen and then ground to extract protein. Immunoblots analysis were followed the same methods as described by Teng (Waadt et al., 2014). BIFC for rice protoplast transformation was followed the method by .
Microscopic techniques were performed refer to Offenborn et al. (2015). Images were processed using the Adobe Photoshop software package.
In vivo co-immunoprecipitation (Co-IP) assay In vitro Cell-free degradation assay For recombinant proteins used in the assay, cDNAs were recombined into pET28a vectors to obtain fusion proteins with 6 × His tag. Recombinant proteins were expressed in Escherichia coli strain Rosetta (DE3) and puri ed using Ni-NTA resin (QIAGEN). The protein concentration was determined using the Bio-Rad protein assay kit.
Cell-free degradation assays were carried out as previously described

Availability of data and materials
All data generated or analyzed in this study are included in this published article and its additional information les.  Responses In B and C, total RNA was extracted from seedlings with 1 μM eBL treatment for 6 h, and cDNA was synthesized by reverse transcription in vitro. The relative abundance of transcripts was estimated as the relative fold change of transcripts in a sample compared to those at Hejiang 19 without BR treatment.  Sequence and structure analysis of OsWDRP3 A. Protein structure of OsWDRP3 depicting the predicted WD40 region. The WD40 domains were predicted using the SMART motif search program (http://smart.embl-heidelberg.de/).
B. Amino acid sequence alignment of OsWDRP3 with WD40 proteins in Arabidopsis. Alignment was carried out using clustalW. Amino acid residues conserved among all the proteins listed are shaded.    C. In vitro cell-free degradation of OsBAK1 259-624 -6×His, which was incubated (0,5,15,30, 60 and 120 min) in crude extracts from Hejiang 19 when OsWDRP3-6×His was added.

Figure 8
Diagram of OsWDRP3 regulating BR signaling by degrading OsBAK1