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拟南芥DELLA蛋白的降解由一种1型蛋白磷酸酶TOPP4控制。

Arabidopsis DELLA protein degradation is controlled by a type-one protein phosphatase, TOPP4.

作者信息

Qin Qianqian, Wang Wei, Guo Xiaola, Yue Jing, Huang Yan, Xu Xiufei, Li Jia, Hou Suiwen

机构信息

Ministry of Education Key Laboratory of Cell Activities and Stress Adaptations, School of Life Sciences, Lanzhou University, Lanzhou, People's Republic of China.

出版信息

PLoS Genet. 2014 Jul 10;10(7):e1004464. doi: 10.1371/journal.pgen.1004464. eCollection 2014 Jul.

DOI:10.1371/journal.pgen.1004464
PMID:25010794
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4091783/
Abstract

Gibberellins (GAs) are a class of important phytohormones regulating a variety of physiological processes during normal plant growth and development. One of the major events during GA-mediated growth is the degradation of DELLA proteins, key negative regulators of GA signaling pathway. The stability of DELLA proteins is thought to be controlled by protein phosphorylation and dephosphorylation. Up to date, no phosphatase involved in this process has been identified. We have identified a dwarfed dominant-negative Arabidopsis mutant, named topp4-1. Reduced expression of TOPP4 using an artificial microRNA strategy also resulted in a dwarfed phenotype. Genetic and biochemical analyses indicated that TOPP4 regulates GA signal transduction mainly via promoting DELLA protein degradation. The severely dwarfed topp4-1 phenotypes were partially rescued by the DELLA deficient mutants rga-t2 and gai-t6, suggesting that the DELLA proteins RGA and GAI are required for the biological function of TOPP4. Both RGA and GAI were greatly accumulated in topp4-1 but significantly decreased in 35S-TOPP4 transgenic plants compared to wild-type plants. Further analyses demonstrated that TOPP4 is able to directly bind and dephosphorylate RGA and GAI, confirming that the TOPP4-controlled phosphorylation status of DELLAs is associated with their stability. These studies provide direct evidence for a crucial role of protein dephosphorylation mediated by TOPP4 in the GA signaling pathway.

摘要

赤霉素(GAs)是一类重要的植物激素,在正常植物生长发育过程中调节多种生理过程。GA介导的生长过程中的一个主要事件是DELLA蛋白的降解,DELLA蛋白是GA信号通路的关键负调控因子。DELLA蛋白的稳定性被认为受蛋白质磷酸化和去磷酸化的控制。到目前为止,尚未鉴定出参与此过程的磷酸酶。我们鉴定出一个矮化的显性负性拟南芥突变体,命名为topp4-1。使用人工microRNA策略降低TOPP4的表达也导致矮化表型。遗传和生化分析表明,TOPP4主要通过促进DELLA蛋白降解来调节GA信号转导。DELLA缺陷型突变体rga-t2和gai-t6部分挽救了严重矮化的topp4-1表型,表明DELLA蛋白RGA和GAI是TOPP4生物学功能所必需的。与野生型植物相比,RGA和GAI在topp4-1中大量积累,但在35S-TOPP4转基因植物中显著减少。进一步分析表明,TOPP4能够直接结合RGA和GAI并使其去磷酸化,证实TOPP4控制的DELLA磷酸化状态与其稳定性相关。这些研究为TOPP4介导的蛋白质去磷酸化在GA信号通路中的关键作用提供了直接证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef29/4091783/979346c5676b/pgen.1004464.g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef29/4091783/96851b3d1209/pgen.1004464.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef29/4091783/4f3d615afe64/pgen.1004464.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef29/4091783/2723670096e8/pgen.1004464.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef29/4091783/6d1d3859a66a/pgen.1004464.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef29/4091783/40592d175799/pgen.1004464.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef29/4091783/e42e2690b8e8/pgen.1004464.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef29/4091783/56e777425a09/pgen.1004464.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef29/4091783/de0728264ff5/pgen.1004464.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef29/4091783/b988e78e7a1b/pgen.1004464.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef29/4091783/979346c5676b/pgen.1004464.g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef29/4091783/96851b3d1209/pgen.1004464.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef29/4091783/4f3d615afe64/pgen.1004464.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef29/4091783/2723670096e8/pgen.1004464.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef29/4091783/6d1d3859a66a/pgen.1004464.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef29/4091783/40592d175799/pgen.1004464.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef29/4091783/e42e2690b8e8/pgen.1004464.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef29/4091783/56e777425a09/pgen.1004464.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef29/4091783/de0728264ff5/pgen.1004464.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef29/4091783/b988e78e7a1b/pgen.1004464.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef29/4091783/979346c5676b/pgen.1004464.g010.jpg

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