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Evolutionary analysis and functional characterization of SiBRI1 as a Brassinosteroid receptor gene in foxtail millet

文献类型： 外文期刊

作者： Zhao, Zhiying 1 ; Tang, Sha 2 ; Zhang, Yiming 3 ; Yue, Jingjing 1 ; Xu, Jiaqi 1 ; Tang, Wenqiang 1 ; Sun, Yanxiang 3 ; Wa 1 ;

作者机构： 1.Hebei Normal Univ, Hebei Collaborat Innovat Ctr Cell Signaling & Env, Hebei Key Lab Mol & Cellular Biol, Minist Educ,Key Lab Mol & Cellular Biol,Coll Life, Shijiazhuang 050024, Hebei, Peoples R China

2.Chinese Acad Agr Sci, Inst Crop Sci, Beijing 100081, Peoples R China

3.Langfang Normal Univ, Coll Life Sci, Langfang 065000, Peoples R China

4.Hebei Acad Agr & Forestry Sci, Inst Millet Crops, Foxtail Millet Improvement Ctr China, Shijiazhuang 050031, Hebei, Peoples R China

关键词： Brassinosteroids; BRI1; Foxtail millet; Phylogenetic analysis

期刊名称：BMC PLANT BIOLOGY （ 影响因子：4.215； 五年影响因子：4.96 ）

ISSN： 1471-2229

年卷期： 2021 年 21 卷 1 期

页码：

收录情况： SCI

摘要： Brassinosteroids (BRs) play important roles in plant growth and development. Although BR receptors have been intensively studied in Arabidopsis, those in foxtail millet remain largely unknown. Here, we show that the BR signaling function of BRASSINOSTEROID INSENSITIVE 1 (BRI1) is conserved between Arabidopsis and foxtail millet, a new model species for C4 and Panicoideae grasses. We identified four putative BR receptor genes in the foxtail millet genome: SiBRI1, SiBRI1-LIKE RECEPTOR KINASE 1 (SiBRL1), SiBRL2 and SiBRL3. Phylogenetic analysis was used to classify the BR receptors in dicots and monocots into three branches. Analysis of their expression patterns by quantitative real-time PCR (qRT-PCR) showed that these receptors were ubiquitously expressed in leaves, stems, dark-grown seedlings, roots and non-flowering spikelets. GFP fusion experiments verified that SiBRI1 localized to the cell membrane. We also explored the SiBRI1 function in Arabidopsis through complementation experiments. Ectopic overexpression of SiBRI1 in an Arabidopsis BR receptor loss-of-function mutant, bri1-116, mostly reversed the developmental defects of the mutant. When SiBRI1 was overexpressed in foxtail millet, the plants showed a drooping leaf phenotype and root development inhibition, lateral root initiation inhibition, and the expression of BR synthesis genes was inhibited. We further identified BRI1-interacting proteins by immunoprecipitation (IP)-mass spectrometry (MS). Our results not only demonstrate that SiBRI1 plays a conserved role in BR signaling in foxtail millet but also provide insight into the molecular mechanism of SiBRI1.

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