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氮饥饿诱导的拟南芥泛素特异性蛋白酶 UBP12 和 UBP13 调控叶片衰老过程中 ORE1 水平。

Arabidopsis ubiquitin-specific proteases UBP12 and UBP13 shape ORE1 levels during leaf senescence induced by nitrogen deficiency.

机构信息

Laboratory of Plant Molecular Biology, Rockefeller University, 1230 York Avenue, New York, NY, 10065, USA.

Temasek Life Sciences Laboratory, 1 Research Link, National University of Singapore, Singapore, 117604, Singapore.

出版信息

New Phytol. 2019 Aug;223(3):1447-1460. doi: 10.1111/nph.15879. Epub 2019 Jun 17.

DOI:10.1111/nph.15879
PMID:31050353
Abstract

Nitrogen deficiency (-N) in plants triggers leaf senescence which is regulated by the transcription factor ORE1. Little is known about post-translational regulation of ORE1 in this process. Here, we show that UBP12/UBP13 (ubiquitin-specific protease 12/13) antagonize the action of NLA (nitrogen limitation adaptation) E3 ligase to maintain ORE1 homeostasis. In vitro pull-down and in vivo co-immunoprecipitation assays demonstrated specific binding between UBP12/UBP13 and ORE1. We further analyzed in various genotypes total Chl content and expression levels of senescence-related genes under -N conditions. We found that UBP12/UBP13 can deubiquitinate polyubiquitinated ORE1 in vitro and increase the stability of ORE1 in vivo in MG132/cycloheximide-chase experiments. Plants overexpressing UBP12/UBP13 display accelerated leaf senescence which is reversed by the ore1 mutation. By contrast, the senescence phenotype of plants overexpressing ORE1 is exacerbated by UBP12/UBP13 overexpression. The expression of senescence-related genes tracks the senescence phenotype. ORE1 protein levels can be elevated by UBP12/UBP13 overexpression but decreased in ubp12-2w/13-3. In conclusion, UBP12/UBP13 deubiquitinate ORE1 to stabilize this transcription factor and promote its activity as a positive regulator for leaf senescence under -N conditions. Our study shows that UBP12/UBP13 counteracts the effect of NLA E3 ligase to accelerate leaf senescence under nitrogen starvation.

摘要

植物氮缺乏(-N)会引发叶片衰老,这一过程受转录因子 ORE1 的调控。然而,关于该过程中 ORE1 的翻译后调控知之甚少。在这里,我们表明 UBP12/UBP13(泛素特异性蛋白酶 12/13)拮抗 NLA(氮限制适应)E3 连接酶的作用,以维持 ORE1 的内稳态。体外下拉和体内共免疫沉淀实验证明了 UBP12/UBP13 与 ORE1 之间的特异性结合。我们进一步在各种基因型下分析了 -N 条件下总叶绿素含量和衰老相关基因的表达水平。我们发现 UBP12/UBP13 可以在体外使多泛素化 ORE1 去泛素化,并在 MG132/环己酰亚胺追踪实验中增加 ORE1 的体内稳定性。过表达 UBP12/UBP13 的植物表现出加速的叶片衰老,而 ore1 突变则逆转了这一现象。相比之下,过表达 ORE1 的植物的衰老表型会因 UBP12/UBP13 的过表达而加剧。衰老相关基因的表达与衰老表型一致。ORE1 蛋白水平可以通过 UBP12/UBP13 的过表达而升高,但在 ubp12-2w/13-3 中降低。总之,UBP12/UBP13 使 ORE1 去泛素化,从而稳定这种转录因子,并促进其作为氮饥饿下叶片衰老的正调控因子的活性。我们的研究表明,UBP12/UBP13 拮抗 NLA E3 连接酶的作用,以加速氮饥饿下的叶片衰老。

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