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UBP12 和 UBP13 去泛素化酶使 CRY2 蓝光受体失稳,从而调控拟南芥的生长。

UBP12 and UBP13 deubiquitinases destabilize the CRY2 blue light receptor to regulate Arabidopsis growth.

机构信息

Cold Spring Harbor Laboratory, 1 Bungtown Road, Cold Spring Harbor, NY 11724, USA.

Cold Spring Harbor Laboratory, 1 Bungtown Road, Cold Spring Harbor, NY 11724, USA.

出版信息

Curr Biol. 2022 Aug 8;32(15):3221-3231.e6. doi: 10.1016/j.cub.2022.05.046. Epub 2022 Jun 13.

DOI:10.1016/j.cub.2022.05.046
PMID:35700731
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9378456/
Abstract

Light is a crucial exogenous signal sensed by cryptochrome (CRY) blue light receptors to modulate growth and the circadian clock in plants and animals. However, how CRYs interpret light quantity to regulate growth in plants remains poorly understood. Furthermore, CRY2 protein levels and activity are tightly regulated in light to fine-tune hypocotyl growth; however, details of the mechanisms that explain precise control of CRY2 levels are not fully understood. We show that in Arabidopsis, UBP12 and UBP13 deubiquitinases physically interact with CRY2 in light. UBP12/13 negatively regulates CRY2 by promoting its ubiquitination and turnover to modulate hypocotyl growth. Growth and development were explicitly affected in blue light when UBP12/13 were disrupted or overexpressed, indicating their role alongside CRY2. UBP12/13 also interacted with and stabilized COP1, which is partially required for CRY2 turnover. Our combined genetic and molecular data support a mechanistic model in which UBP12/13 interact with CRY2 and COP1, leading to the stabilization of COP1. Stabilized COP1 then promotes the ubiquitination and degradation of CRY2 under blue light. Despite decades of studies on deubiquitinases, the knowledge of how their activity is regulated is limited. Our study provides insight into how exogenous signals and ligands, along with their receptors, regulate deubiquitinase activity by protein-protein interaction. Collectively, our results provide a framework of cryptochromes and deubiquitinases to detect and interpret light signals to control plant growth at the most appropriate time.

摘要

光是一种至关重要的外源性信号,被隐花色素(CRY)蓝光受体感知,以调节动植物的生长和生物钟。然而,CRY 如何解释光量子来调节植物的生长仍知之甚少。此外,CRY2 蛋白水平和活性在光照下受到严格调控,以精细调节下胚轴的生长;然而,解释 CRY2 水平精确调控的机制细节尚不完全清楚。我们表明,在拟南芥中,UBP12 和 UBP13 去泛素酶在光照下与 CRY2 相互作用。UBP12/13 通过促进 CRY2 的泛素化和周转来负调控 CRY2,从而调节下胚轴的生长。当 UBP12/13 被破坏或过表达时,在蓝光下生长和发育受到明显影响,表明它们与 CRY2 一起发挥作用。UBP12/13 还与 COP1 相互作用并稳定 COP1,COP1 部分是 CRY2 周转所必需的。我们的综合遗传和分子数据支持一个机制模型,其中 UBP12/13 与 CRY2 和 COP1 相互作用,导致 COP1 的稳定。稳定的 COP1 随后促进 CRY2 在蓝光下的泛素化和降解。尽管几十年来对去泛素酶进行了研究,但对其活性如何调控的了解有限。我们的研究提供了一个见解,即外源性信号和配体及其受体如何通过蛋白质-蛋白质相互作用来调节去泛素酶的活性。总之,我们的研究结果为隐花色素和去泛素酶提供了一个框架,以检测和解释光信号,从而在最合适的时间控制植物生长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/822e/9378456/cb36ad28b8e4/nihms-1811054-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/822e/9378456/6d0b90268c73/nihms-1811054-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/822e/9378456/22cf7ea151f7/nihms-1811054-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/822e/9378456/fbc37e9f6145/nihms-1811054-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/822e/9378456/d3d03b759667/nihms-1811054-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/822e/9378456/452dba8c820c/nihms-1811054-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/822e/9378456/cb36ad28b8e4/nihms-1811054-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/822e/9378456/6d0b90268c73/nihms-1811054-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/822e/9378456/22cf7ea151f7/nihms-1811054-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/822e/9378456/fbc37e9f6145/nihms-1811054-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/822e/9378456/d3d03b759667/nihms-1811054-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/822e/9378456/452dba8c820c/nihms-1811054-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/822e/9378456/cb36ad28b8e4/nihms-1811054-f0006.jpg

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