Center for Cell & Developmental Biology, State Key Laboratory of Agrobiotechnology, School of Life Sciences, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, China.
Shenzhen Technology University, Shenzhen, 518000, China.
J Integr Plant Biol. 2021 Jun;63(6):1104-1119. doi: 10.1111/jipb.13071. Epub 2021 Mar 26.
Flowering time is crucial for successful reproduction in plants, the onset and progression of which are strictly controlled. However, flowering time is a complex and environmentally responsive history trait and the underlying mechanisms still need to be fully characterized. Post-translational regulation of the activities of transcription factors (TFs) is a dynamic and essential mechanism for plant growth and development. CRL3 E3 ligase is a CULLIN3-based E3 ligase involved in orchestrating protein stability via the ubiquitin proteasome pathway. Our study shows that the mutation of MYB106 induced early flowering phenotype while over-expression of MYB106 delayed Arabidopsis flowering. Transcriptome analysis of myb106 mutants reveals 257 differentially expressed genes between wild type and myb106-1 mutants, including Flowering Locus T (FT) which is related to flowering time. Moreover, in vitro electrophoretic mobility shift assays (EMSA), in vivo chromatin immunoprecipitation quantitative polymerase chain reaction (ChIP-qPCR) assays and dual luciferase assays demonstrate that MYB106 directly binds to the promoter of FT to suppress its expression. Furthermore, we confirm that MYB106 interacts with BPM proteins which are further identified by CRL3 E3 ligases as the substrate. Taken together, we have identified MYB106 as a negative regulator in the control of flowering time and a new substrate for CRL3 E3 ligases in Arabidopsis.
开花时间对植物的成功繁殖至关重要,其起始和进程受到严格控制。然而,开花时间是一个复杂的、对环境有响应的历史特征,其潜在机制仍需要充分阐明。转录因子(TFs)活性的翻译后调控是植物生长和发育的一种动态和必要的机制。CRL3 E3 连接酶是一种基于 CULLIN3 的 E3 连接酶,通过泛素蛋白酶体途径参与协调蛋白质稳定性。我们的研究表明,MYB106 的突变诱导了拟南芥的早花表型,而过表达 MYB106 则延迟了开花时间。myb106 突变体的转录组分析显示,野生型和 myb106-1 突变体之间有 257 个差异表达基因,包括与开花时间有关的 Flowering Locus T(FT)。此外,体外电泳迁移率变动分析(EMSA)、体内染色质免疫沉淀定量聚合酶链反应(ChIP-qPCR)分析和双荧光素酶报告基因分析表明,MYB106 直接结合到 FT 的启动子上,抑制其表达。此外,我们还证实了 MYB106 与 BPM 蛋白相互作用,而 BPM 蛋白被 CRL3 E3 连接酶进一步鉴定为底物。综上所述,我们已经确定 MYB106 是控制开花时间的负调控因子,也是拟南芥中 CRL3 E3 连接酶的一个新底物。