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BRI1-EMS-SUPPRESSOR 1(BES1)的 SUMO 化被 SUMO E3 连接酶 SIZ1 负调控拟南芥中的油菜素内酯信号。

Sumoylation of BRI1-EMS-SUPPRESSOR 1 (BES1) by the SUMO E3 Ligase SIZ1 Negatively Regulates Brassinosteroids Signaling in Arabidopsis thaliana.

机构信息

Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, Sichuan, P.R. China.

State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, P.R. China.

出版信息

Plant Cell Physiol. 2019 Oct 1;60(10):2282-2292. doi: 10.1093/pcp/pcz125.

Abstract

Brassinosteroids (BRs), a group of plant steroid hormones, participate in the regulation of plant growth and developmental processes. BR functions through the BES1/BZR1 family of transcription factors, however, the regulation of the BES1 activity by post-translational modifications remains largely unknown. Here, we present evidence that the SUMO E3 ligase SIZ1 negatively regulates BR signaling pathway. T-DNA insertion mutant siz1-2 shows BL (Brassinolide, the most active BR) hypersensitivity and BRZ (Brassinazole, a BR biosynthesis inhibitor) insensitivity during hypocotyl elongation. In addition, expression of BES1-dependent BR-response genes is hyper-regulated in siz1-2 seedlings. The siz1-2bes1-D double mutant exhibits longer hypocotyl than bes1-D. Moreover, SIZ1 physically interacts with BES1 in vivo and in vitro and mediates the sumoylation of BES1. A K302R substitution in BES1 blocks its sumoylation mediated by SIZ1 in plants, indicating that K302 is the principal site for SUMO conjugation. Consistently, we find that sumoylation inhibits BES1 protein stability and activity. Taken together, our data show that the sumoylation of BES1 via SIZ1 negatively regulates the BR signaling pathway.

摘要

油菜素内酯(BRs)是一组植物甾体激素,参与植物生长和发育过程的调节。BR 通过 BES1/BZR1 家族的转录因子发挥作用,然而,BES1 活性的翻译后修饰调控在很大程度上仍是未知的。在这里,我们提出证据表明 SUMO E3 连接酶 SIZ1 负调控 BR 信号通路。T-DNA 插入突变体 siz1-2 在原胚轴伸长过程中表现出 BL(油菜素内酯,最活跃的 BR)超敏性和 BRZ(油菜素唑,BR 生物合成抑制剂)不敏感性。此外,siz1-2 幼苗中 BES1 依赖性 BR 反应基因的表达被过度调控。siz1-2bes1-D 双突变体的原胚轴比 bes1-D 更长。此外,SIZ1 在体内和体外与 BES1 相互作用,并介导 BES1 的 SUMO 化。BES1 中的 K302R 取代阻止了 SIZ1 在植物中对其的 SUMO 化,表明 K302 是 SUMO 缀合的主要位点。一致地,我们发现 SUMO 化抑制 BES1 蛋白稳定性和活性。总之,我们的数据表明,通过 SIZ1 对 BES1 的 SUMO 化负调控 BR 信号通路。

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