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