Jiangsu Key Laboratory of Crop Genetics and Physiology/Key Laboratory of Plant Functional Genomics of the Ministry of Education/Jiangsu Key Laboratory of Crop Genomics and Molecular Breeding, College of Agriculture, Yangzhou University, Yangzhou, 225009, China.
Jiangsu Co-Innovation Center for Modern Production Technology of Grain Crops, Yangzhou University, Yangzhou, 225009, China.
Plant Cell Rep. 2022 Aug;41(8):1763-1774. doi: 10.1007/s00299-022-02891-w. Epub 2022 Jun 23.
G protein couples MAPK cascade through maize heterotrimeric Gβ subunit MGB1. Heterotrimeric G protein Gβ interacts with Gγ subunit to generate Gβγ dimer in modulation of various biological processes. The modulatory events at transcriptome scale of plant Gβ subunit remain largely unknown. To reveal the regulatory basis of Gβ subunit at transcriptome level, we first identified a canonical maize Gβ subunit MGB1 that physically interacted with Type C Gγ protein MGG4. For transcriptome analysis, two independent CRISPR/Cas9-edited MGB1 lines were generated, which all exhibited growth arrest, suggestive of MGB1 essential for maize seedling establishment. Transcriptomic outcomes showed that MGB1 knockout resulted in elevated transcriptional abundance of plant immune response marker PR and immune receptor RPM1. Integrated GO, KEGG, and GSEA analyses pinpointed the enrichment of differentially expressed genes in defense response pathway. Functional association network construction revealed MAPK cascade components and PR protein as hub regulators of MGB1-mediated immune signaling. MGB1 and scaffold protein ZmRACK1 together with MAPK cascade components coordinately modulated maize immune responses. We built a modulatory hierarchy of Gβ subunit at transcriptome and interacting scales, which is informative for our understanding of the regulatory basis of G protein signaling.
G 蛋白通过玉米异三聚体 Gβ亚基 MGB1 偶联 MAPK 级联。异三聚体 G 蛋白 Gβ与 Gγ亚基相互作用,生成 Gβγ二聚体,调节各种生物过程。植物 Gβ亚基在转录组水平上的调节事件在很大程度上仍然未知。为了揭示 Gβ亚基在转录组水平上的调控基础,我们首先鉴定了一个与玉米 Type C Gγ蛋白 MGG4 相互作用的典型 Gβ亚基 MGB1。为了进行转录组分析,我们生成了两个独立的 CRISPR/Cas9 编辑的 MGB1 系,它们都表现出生长停滞,表明 MGB1 对玉米幼苗的建立是必需的。转录组结果表明,MGB1 敲除导致植物免疫反应标记物 PR 和免疫受体 RPM1 的转录丰度升高。综合 GO、KEGG 和 GSEA 分析指出,差异表达基因在防御反应途径中富集。功能关联网络构建揭示了 MAPK 级联成分和 PR 蛋白作为 MGB1 介导的免疫信号的枢纽调节剂。MGB1 和支架蛋白 ZmRACK1 与 MAPK 级联成分一起共同调节玉米的免疫反应。我们构建了一个在转录组和相互作用尺度上的 Gβ亚基调节层次结构,这为我们理解 G 蛋白信号的调控基础提供了信息。