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本文引用的文献

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Multiple effects of antibiotics on chloroplast and nuclear gene expression.抗生素对叶绿体和核基因表达的多种影响。
Funct Plant Biol. 2003 Jan;30(11):1097-1103. doi: 10.1071/FP03149.
2
Growth in vitro of arrested embryos from lethal mutants ofArabidopsis thaliana.拟南芥致死突变体胚胎的体外生长。
Theor Appl Genet. 1986 Aug;72(5):577-86. doi: 10.1007/BF00288994.
3
GLK transcription factors coordinate expression of the photosynthetic apparatus in Arabidopsis.GLK转录因子协调拟南芥中光合机构的表达。
Plant Cell. 2009 Apr;21(4):1109-28. doi: 10.1105/tpc.108.065250. Epub 2009 Apr 17.
4
Targeting of nucleus-encoded proteins to chloroplasts in plants.植物中细胞核编码蛋白向叶绿体的靶向运输
New Phytol. 2008 Jul;179(2):257-285. doi: 10.1111/j.1469-8137.2008.02452.x.
5
Tetrapyrrole profiling in Arabidopsis seedlings reveals that retrograde plastid nuclear signaling is not due to Mg-protoporphyrin IX accumulation.拟南芥幼苗中的四吡咯分析表明,逆向质体-核信号传导并非由于镁原卟啉IX积累所致。
Proc Natl Acad Sci U S A. 2008 Sep 30;105(39):15178-83. doi: 10.1073/pnas.0803054105. Epub 2008 Sep 25.
6
The steady-state level of Mg-protoporphyrin IX is not a determinant of plastid-to-nucleus signaling in Arabidopsis.镁原卟啉IX的稳态水平不是拟南芥中质体到细胞核信号传导的决定因素。
Proc Natl Acad Sci U S A. 2008 Sep 30;105(39):15184-9. doi: 10.1073/pnas.0803245105. Epub 2008 Sep 25.
7
Identification and characterization of Cor413im proteins as novel components of the chloroplast inner envelope.鉴定和表征Cor413im蛋白作为叶绿体内膜的新组分。
Plant Cell Environ. 2008 Oct;31(10):1470-83. doi: 10.1111/j.1365-3040.2008.01854.x. Epub 2008 Jul 14.
8
Protein trafficking to plastids: one theme, many variations.蛋白质向质体的运输:一个主题,多种变体。
Biochem J. 2008 Jul 1;413(1):15-28. doi: 10.1042/BJ20080490.
9
Plastid signals remodel light signaling networks and are essential for efficient chloroplast biogenesis in Arabidopsis.质体信号重塑光信号网络,对拟南芥中叶绿体的高效生物发生至关重要。
Plant Cell. 2007 Dec;19(12):3944-60. doi: 10.1105/tpc.107.054312. Epub 2007 Dec 7.
10
The GLK1 'regulon' encodes disease defense related proteins and confers resistance to Fusarium graminearum in Arabidopsis.GLK1“调控子”编码与疾病防御相关的蛋白质,并赋予拟南芥对禾谷镰刀菌的抗性。
Biochem Biophys Res Commun. 2007 Jul 27;359(2):234-8. doi: 10.1016/j.bbrc.2007.05.084. Epub 2007 May 24.

质体到核逆行信号对质体蛋白导入和核基因表达的协调作用。

Coordination of plastid protein import and nuclear gene expression by plastid-to-nucleus retrograde signaling.

机构信息

The 21st Century Centers of Excellence Program, Cryobiofrontier Research Center, Iwate University, Morioka, Iwate 020-8550, Japan.

出版信息

Plant Physiol. 2009 Nov;151(3):1339-53. doi: 10.1104/pp.109.145987. Epub 2009 Sep 2.

DOI:10.1104/pp.109.145987
PMID:19726569
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2773054/
Abstract

Expression of nuclear-encoded plastid proteins and import of those proteins into plastids are indispensable for plastid biogenesis. One possible cellular mechanism that coordinates these two essential processes is retrograde signaling from plastids to the nucleus. However, the molecular details of how this signaling occurs remain elusive. Using the plastid protein import2 mutant of Arabidopsis (Arabidopsis thaliana), which lacks the atToc159 protein import receptor, we demonstrate that the expression of photosynthesis-related nuclear genes is tightly coordinated with their import into plastids. Down-regulation of photosynthesis-related nuclear genes is also observed in mutants lacking other components of the plastid protein import apparatus. Genetic studies indicate that the coordination of plastid protein import and nuclear gene expression is independent of proposed plastid signaling pathways such as the accumulation of Mg-protoporphyrin IX and the activity of ABA INSENSITIVE4 (ABI4). Instead, it may involve GUN1 and the transcription factor AtGLK. The expression level of AtGLK1 is tightly correlated with the expression of photosynthesis-related nuclear genes in mutants defective in plastid protein import. Furthermore, the activity of GUN1 appears to down-regulate the expression of AtGLK1 when plastids are dysfunctional. Based on these data, we suggest that defects in plastid protein import generate a signal that represses photosynthesis-related nuclear genes through repression of AtGLK1 expression but not through activation of ABI4.

摘要

核编码质体蛋白的表达和这些蛋白向质体的输入对于质体生物发生是必不可少的。协调这两个基本过程的一种可能的细胞机制是质体到核的逆行信号转导。然而,这种信号转导发生的分子细节仍然难以捉摸。使用拟南芥(Arabidopsis thaliana)的质体蛋白导入 2 突变体(缺乏 atToc159 蛋白导入受体),我们证明与光合作用相关的核基因的表达与其向质体的导入紧密协调。在缺乏质体蛋白导入装置的其他成分的突变体中,也观察到与光合作用相关的核基因的下调。遗传研究表明,质体蛋白导入和核基因表达的协调与拟议的质体信号通路(如 Mg-原卟啉 IX 的积累和 ABA 不敏感 4(ABI4)的活性)无关。相反,它可能涉及 GUN1 和转录因子 AtGLK。在质体蛋白导入缺陷的突变体中,AtGLK1 的表达水平与与光合作用相关的核基因的表达紧密相关。此外,当质体功能失调时,GUN1 的活性似乎会通过抑制 AtGLK1 的表达而不是通过激活 ABI4 来下调其表达。基于这些数据,我们认为质体蛋白导入的缺陷会产生一种信号,通过抑制 AtGLK1 的表达而不是通过激活 ABI4 来抑制与光合作用相关的核基因的表达。