Department of Plant Sciences, University of Tennessee, Knoxville, TN, 37996, USA.
UT-ORNL Graduate School of Genome Science and Technology, University of Tennessee, Knoxville, TN, 37996, USA.
New Phytol. 2023 Sep;239(6):2335-2352. doi: 10.1111/nph.19087. Epub 2023 Jun 20.
BAK1-INTERACTING RECEPTOR LIKE KINASE1 (BIR1) is a negative regulator of various aspects of disease resistance and immune responses. Here, we investigated the functional role of soybean (Glycine max) BIR1 (GmBIR1) during soybean interaction with soybean cyst nematode (SCN, Heterodera glycines) and the molecular mechanism through which GmBIR1 regulates plant immunity. Overexpression of wild-type variant of GmBIR1 (WT-GmBIR1) using transgenic soybean hairy roots significantly increased soybean susceptibility to SCN, whereas overexpression of kinase-dead variant (KD-GmBIR1) significantly increased plant resistance. Transcriptome analysis revealed that genes oppositely regulated in WT-GmBIR1 and KD-GmBIR1 upon SCN infection were enriched primarily in defense and immunity-related functions. Quantitative phosphoproteomic analysis identified 208 proteins as putative substrates of the GmBIR1 signaling pathway, 114 of which were differentially phosphorylated upon SCN infection. In addition, the phosphoproteomic data pointed to a role of the GmBIR1 signaling pathway in regulating alternative pre-mRNA splicing. Genome-wide analysis of splicing events provided compelling evidence supporting a role of the GmBIR1 signaling pathway in establishing alternative splicing during SCN infection. Our results provide novel mechanistic insights into the function of the GmBIR1 signaling pathway in regulating soybean transcriptome and spliceome via differential phosphorylation of splicing factors and regulation of splicing events of pre-mRNA decay- and spliceosome-related genes.
BAK1-INTERACTING RECEPTOR LIKE KINASE1(BIR1)是多种疾病抗性和免疫反应的负调控因子。在这里,我们研究了大豆(Glycine max)BIR1(GmBIR1)在与大豆胞囊线虫(SCN,Heterodera glycines)相互作用过程中的功能作用,以及 GmBIR1 调节植物免疫的分子机制。利用转基因大豆毛状根过表达野生型 GmBIR1(WT-GmBIR1)显著增加了大豆对 SCN 的易感性,而激酶失活型 GmBIR1(KD-GmBIR1)的过表达则显著增加了植物的抗性。转录组分析表明,在 SCN 感染后,WT-GmBIR1 和 KD-GmBIR1 相反调控的基因主要富集在防御和免疫相关功能中。定量磷酸化蛋白质组分析鉴定了 208 个可能是 GmBIR1 信号通路底物的蛋白,其中 114 个在 SCN 感染时发生了差异磷酸化。此外,磷酸化蛋白质组数据表明,GmBIR1 信号通路在调节替代前体 mRNA 剪接中发挥作用。剪接事件的全基因组分析为 GmBIR1 信号通路在 SCN 感染过程中通过差异磷酸化剪接因子和调节前体 mRNA 降解和剪接体相关基因的剪接事件来调节大豆转录组和剪接体提供了有力的证据。我们的研究结果为 GmBIR1 信号通路通过差异磷酸化剪接因子和调节前体 mRNA 降解和剪接体相关基因的剪接事件来调节大豆转录组和剪接体提供了新的机制见解。