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2
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Proteasome inhibition rapidly exacerbates photoinhibition and impedes recovery during high light stress in Chlamydomonas reinhardtii.蛋白酶体抑制作用在强光胁迫下迅速加剧莱茵衣藻的光抑制作用并阻碍其恢复。
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本文引用的文献

1
Stable incorporation of ATPase subunits into 19 S regulatory particle of human proteasome requires nucleotide binding and C-terminal tails.稳定地将 ATPase 亚基整合到人蛋白酶体的 19 S 调节颗粒中需要核苷酸结合和 C 末端尾巴。
J Biol Chem. 2012 Mar 16;287(12):9269-79. doi: 10.1074/jbc.M111.316208. Epub 2012 Jan 24.
2
Complete subunit architecture of the proteasome regulatory particle.完整的蛋白酶体调节颗粒亚基结构。
Nature. 2012 Jan 11;482(7384):186-91. doi: 10.1038/nature10774.
3
The RPT2 subunit of the 26S proteasome directs complex assembly, histone dynamics, and gametophyte and sporophyte development in Arabidopsis.26S 蛋白酶体的 RPT2 亚基指导复合物组装、组蛋白动力学以及拟南芥的配子体和孢子体发育。
Plant Cell. 2011 Dec;23(12):4298-317. doi: 10.1105/tpc.111.089482. Epub 2011 Dec 9.
4
An asymmetric interface between the regulatory and core particles of the proteasome.蛋白酶体的调节颗粒和核心颗粒之间的非对称界面。
Nat Struct Mol Biol. 2011 Oct 30;18(11):1259-67. doi: 10.1038/nsmb.2147.
5
Blm10 protein promotes proteasomal substrate turnover by an active gating mechanism.Blm10 蛋白通过一种活性门控机制促进蛋白酶体底物的周转率。
J Biol Chem. 2011 Dec 16;286(50):42830-9. doi: 10.1074/jbc.M111.300178. Epub 2011 Oct 24.
6
Involvement of Arabidopsis NAC transcription factor in the regulation of 20S and 26S proteasomes.拟南芥 NAC 转录因子参与 20S 和 26S 蛋白酶体的调节。
Plant Sci. 2011 Oct;181(4):421-7. doi: 10.1016/j.plantsci.2011.07.001. Epub 2011 Jul 19.
7
C termini of proteasomal ATPases play nonequivalent roles in cellular assembly of mammalian 26 S proteasome.蛋白酶体 ATP 酶的 C 末端在哺乳动物 26S 蛋白酶体的细胞组装中发挥非等效作用。
J Biol Chem. 2011 Jul 29;286(30):26652-66. doi: 10.1074/jbc.M111.246793. Epub 2011 May 31.
8
From nucleosome to chromosome: a dynamic organization of genetic information.从核小体到染色体:遗传信息的动态组织。
Plant J. 2011 Apr;66(1):4-17. doi: 10.1111/j.1365-313X.2011.04526.x.
9
ATP binds to proteasomal ATPases in pairs with distinct functional effects, implying an ordered reaction cycle.ATP 以成对的形式与蛋白酶体 ATP 酶结合,具有不同的功能效应,这意味着存在一个有序的反应循环。
Cell. 2011 Feb 18;144(4):526-38. doi: 10.1016/j.cell.2011.02.005.
10
Endoplasmic reticulum protein quality control and its relationship to environmental stress responses in plants.内质网蛋白质量控制及其与植物环境胁迫响应的关系。
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拟南芥 26S 蛋白酶体调节颗粒的遗传分析揭示了其在光胁迫过程中的重要性,以及 RPT2 N 端在发育过程中的特定作用。

Genetic analyses of the Arabidopsis 26S proteasome regulatory particle reveal its importance during light stress and a specific role for the N-terminus of RPT2 in development.

机构信息

Department of Genetics, University of Wisconsin, Madison, WI USA.

出版信息

Plant Signal Behav. 2012 Aug;7(8):973-8. doi: 10.4161/psb.20934. Epub 2012 Jul 27.

DOI:10.4161/psb.20934
PMID:22836496
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3474698/
Abstract

The 26S proteasome subunit RPT2 is a component of the hexameric ring of AAA-ATPases that forms the base of the 19S regulatory particle (RP). This subunit has specific roles in the yeast and mammalian proteasomes by helping promote assembly of the RP with the 20S core protease (CP) and gate the CP to prevent indiscriminate degradation of cytosolic and nuclear proteins. In plants, this subunit plays an important role in diverse processes that include shoot and root apical meristem maintenance, cell size regulation, trichome branching, and stress responses. Recently, we reported that mutants in RPT2 and several other RP subunits have reduced histone levels, suggesting that at least some of the pleiotropic phenotypes observed in these plants result from aberrant nucleosome assembly. Here, we expand our genetic analysis of RPT2 in Arabidopsis to shed additional light on the roles of the N- and C-terminal ends. We also present data showing that plants bearing mutations in RP subunit genes have their seedling phenotypes exacerbated by prolonged light exposure.

摘要

26S 蛋白酶体亚基 RPT2 是六聚体 AAA-ATPase 环的一个组成部分,该环形成 19S 调节颗粒 (RP) 的底座。该亚基在酵母和哺乳动物蛋白酶体中具有特定的作用,通过帮助促进 RP 与 20S 核心蛋白酶 (CP) 的组装,并对 CP 进行门控,以防止细胞质和核蛋白的无差别降解。在植物中,该亚基在多种过程中发挥重要作用,包括芽和根顶端分生组织的维持、细胞大小调节、毛状体分枝和应激反应。最近,我们报道 RPT2 和其他几个 RP 亚基的突变体减少了组蛋白水平,这表明在这些植物中观察到的至少一些表型的多效性是由于核小体组装异常所致。在这里,我们扩展了对拟南芥中 RPT2 的遗传分析,以进一步阐明 N 端和 C 端的作用。我们还提供了数据,表明在 RP 亚基基因发生突变的植物中,幼苗表型在长时间光照下会加剧。