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本文引用的文献

1
Eukaryotic-type plastid nucleoid protein pTAC3 is essential for transcription by the bacterial-type plastid RNA polymerase.真核型质体核区蛋白 pTAC3 是细菌型质体 RNA 聚合酶转录所必需的。
Proc Natl Acad Sci U S A. 2012 May 8;109(19):7541-6. doi: 10.1073/pnas.1119403109. Epub 2012 Apr 23.
2
Insights into the regulation of protein abundance from proteomic and transcriptomic analyses.从蛋白质组学和转录组学分析中洞察蛋白质丰度的调控。
Nat Rev Genet. 2012 Mar 13;13(4):227-32. doi: 10.1038/nrg3185.
3
Plastids are major regulators of light signaling in Arabidopsis.质体是拟南芥中光信号的主要调节因子。
Plant Physiol. 2012 May;159(1):366-90. doi: 10.1104/pp.112.193599. Epub 2012 Mar 1.
4
Targeting of lumenal proteins across the thylakoid membrane.靶向类囊体膜腔中的蛋白质。
J Exp Bot. 2012 Feb;63(4):1689-98. doi: 10.1093/jxb/err444. Epub 2012 Jan 24.
5
The cutting crew - ribonucleases are key players in the control of plastid gene expression.剪切小组——核糖核酸酶是控制质体基因表达的关键因素。
J Exp Bot. 2012 Feb;63(4):1663-73. doi: 10.1093/jxb/err401. Epub 2011 Dec 3.
6
The Arabidopsis Information Resource (TAIR): improved gene annotation and new tools.拟南芥信息资源(TAIR):改进的基因注释和新工具。
Nucleic Acids Res. 2012 Jan;40(Database issue):D1202-10. doi: 10.1093/nar/gkr1090. Epub 2011 Dec 2.
7
Plastid proteome assembly without Toc159: photosynthetic protein import and accumulation of N-acetylated plastid precursor proteins.质体蛋白体装配不需要 Toc159:光合蛋白的导入和 N-乙酰化质体前体蛋白的积累。
Plant Cell. 2011 Nov;23(11):3911-28. doi: 10.1105/tpc.111.092882. Epub 2011 Nov 29.
8
Phylogenetic and functional features of the plastid transcription kinase cpCK2 from Arabidopsis signify a role of cysteinyl SH-groups in regulatory phosphorylation of plastid sigma factors.拟南芥质体转录激酶 cpCK2 的系统发生和功能特征表明半胱氨酸巯基在质体 σ 因子的调节磷酸化中的作用。
FEBS J. 2012 Feb;279(3):395-409. doi: 10.1111/j.1742-4658.2011.08433.x. Epub 2011 Dec 19.
9
Nucleoid-enriched proteomes in developing plastids and chloroplasts from maize leaves: a new conceptual framework for nucleoid functions.富含类核的玉米叶片发育中的质体和叶绿体蛋白质组:类核功能的新概念框架。
Plant Physiol. 2012 Jan;158(1):156-89. doi: 10.1104/pp.111.188474. Epub 2011 Nov 7.
10
The workflow for quantitative proteome analysis of chloroplast development and differentiation, chloroplast mutants, and protein interactions by spectral counting.通过光谱计数对叶绿体发育与分化、叶绿体突变体及蛋白质相互作用进行定量蛋白质组分析的工作流程。
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不同白化/淡绿色突变体中常见和特异的蛋白积累模式揭示了蛋白质组水平的调控子组织。

Common and specific protein accumulation patterns in different albino/pale-green mutants reveals regulon organization at the proteome level.

机构信息

Faculty of Agriculture, Shizuoka University, Suruga-ku, Shizuoka 422-8529, Japan.

出版信息

Plant Physiol. 2012 Dec;160(4):2189-201. doi: 10.1104/pp.112.204032. Epub 2012 Oct 1.

DOI:10.1104/pp.112.204032
PMID:23027667
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3510140/
Abstract

Research interest in proteomics is increasingly shifting toward the reverse genetic characterization of gene function at the proteome level. In plants, several distinct gene defects perturb photosynthetic capacity, resulting in the loss of chlorophyll and an albino or pale-green phenotype. Because photosynthesis is interconnected with the entire plant metabolism and its regulation, all albino plants share common characteristics that are determined by the switch from autotrophic to heterotrophic growth. Reverse genetic characterizations of such plants often cannot distinguish between specific consequences of a gene defect from generic effects in response to perturbations in photosynthetic capacity. Here, we set out to define common and specific features of protein accumulation in three different albino/pale-green plant lines. Using quantitative proteomics, we report a common molecular phenotype that connects the loss of photosynthetic capacity with other chloroplast and cellular functions, such as protein folding and stability, plastid protein import, and the expression of stress-related genes. Surprisingly, we do not find significant differences in the expression of key transcriptional regulators, suggesting that substantial regulation occurs at the posttranscriptional level. We examine the influence of different normalization schemes on the quantitative proteomics data and report all identified proteins along with their fold changes and P values in albino plants in comparison with the wild type. Our analysis provides initial guidance for the distinction between general and specific adaptations of the proteome in photosynthesis-impaired plants.

摘要

蛋白质组学的研究兴趣越来越多地转向在蛋白质组水平上对基因功能进行反向遗传学分析。在植物中,有几种不同的基因缺陷会干扰光合作用能力,导致叶绿素丧失和白化或淡绿色表型。由于光合作用与整个植物代谢及其调节相互关联,所有白化植物都具有由自养生长向异养生长转变所决定的共同特征。对这些植物进行反向遗传学分析往往无法区分基因缺陷的具体后果与光合作用能力受到干扰后的一般影响。在这里,我们着手定义三种不同白化/淡绿色植物系中蛋白质积累的共同和特定特征。我们使用定量蛋白质组学报告了一个共同的分子表型,将光合作用能力的丧失与其他叶绿体和细胞功能(如蛋白质折叠和稳定性、质体蛋白导入和与应激相关的基因表达)联系起来。令人惊讶的是,我们没有发现关键转录调节剂表达的显著差异,这表明大量调控发生在转录后水平。我们检查了不同归一化方案对定量蛋白质组学数据的影响,并报告了在白化植物中与野生型相比所有鉴定到的蛋白质及其在白化植物中的倍数变化和 P 值。我们的分析为区分光合作用受损植物中蛋白质组的一般和特定适应提供了初步指导。