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本文引用的文献

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Multifunctionality of plastid nucleoids as revealed by proteome analyses.蛋白质组分析揭示的质体类核的多功能性
Biochim Biophys Acta. 2016 Aug;1864(8):1016-38. doi: 10.1016/j.bbapap.2016.03.009. Epub 2016 Mar 14.
2
Plastid control of abaxial-adaxial patterning.质体对叶片远轴面-近轴面模式的调控
Sci Rep. 2015 Nov 2;5:15975. doi: 10.1038/srep15975.
3
The complex of ASYMMETRIC LEAVES (AS) proteins plays a central role in antagonistic interactions of genes for leaf polarity specification in Arabidopsis.不对称叶片(AS)蛋白复合体在拟南芥叶极性特征基因的拮抗相互作用中起核心作用。
Wiley Interdiscip Rev Dev Biol. 2015 Nov-Dec;4(6):655-71. doi: 10.1002/wdev.196. Epub 2015 Jun 24.
4
Chloroplast transcription, untangling the Gordian Knot.叶绿体转录,解开戈尔迪之结。
New Phytol. 2015 May;206(3):889-891. doi: 10.1111/nph.13388.
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ZmpTAC12 binds single-stranded nucleic acids and is essential for accumulation of the plastid-encoded polymerase complex in maize.ZmpTAC12结合单链核酸,对玉米中质体编码聚合酶复合体的积累至关重要。
New Phytol. 2015 May;206(3):1024-1037. doi: 10.1111/nph.13248. Epub 2015 Jan 19.
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Nuclear-encoded factors associated with the chloroplast transcription machinery of higher plants.与高等植物叶绿体转录机制相关的核编码因子。
Front Plant Sci. 2014 Jul 3;5:316. doi: 10.3389/fpls.2014.00316. eCollection 2014.
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Recent advances in the study of chloroplast gene expression and its evolution.叶绿体基因表达及其进化研究的最新进展。
Front Plant Sci. 2014 Feb 25;5:61. doi: 10.3389/fpls.2014.00061. eCollection 2014.
8
A major role for the plastid-encoded RNA polymerase complex in the expression of plastid transfer RNAs.质体编码的RNA聚合酶复合体在质体转移RNA表达中的主要作用。
Plant Physiol. 2014 Jan;164(1):239-48. doi: 10.1104/pp.113.228726. Epub 2013 Nov 18.
9
The reduced plastid-encoded polymerase-dependent plastid gene expression leads to the delayed greening of the Arabidopsis fln2 mutant.质体编码聚合酶依赖的质体基因表达减少导致拟南芥 fln2 突变体变绿延迟。
PLoS One. 2013 Sep 3;8(9):e73092. doi: 10.1371/journal.pone.0073092. eCollection 2013.
10
Essential nucleoid proteins in early chloroplast development.早期叶绿体发育中的必需核质体蛋白。
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pTAC10,质体编码 RNA 聚合酶的关键亚基,促进叶绿体发育。

pTAC10, a Key Subunit of Plastid-Encoded RNA Polymerase, Promotes Chloroplast Development.

机构信息

Department of Agricultural Biotechnology and Research Institute of Agriculture and Life Sciences, Seoul National University, Seoul 151-921, Korea (S.H.C., S.L., T.Y.U., Y.D.C., G.J.); and.

Graduate School of International Agricultural Technology and Crop Biotechnology Institute/Green BioScience and Technology, Seoul National University, Pyeongchang 232-916, Korea (J.-K.K.).

出版信息

Plant Physiol. 2017 May;174(1):435-449. doi: 10.1104/pp.17.00248. Epub 2017 Mar 23.

DOI:10.1104/pp.17.00248
PMID:28336770
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5411158/
Abstract

Regulation of photosynthetic gene expression by plastid-encoded RNA polymerase (PEP) is essential for chloroplast development. The activity of PEP largely relies on at least 12 PEP-associated proteins (PAPs) encoded in the nuclear genome of plant cells. A recent model proposed that these PAPs regulate the establishment of the PEP complex through broad PAP-PEP or PAP-PAP interactions. In this study, we identified the Arabidopsis () seedling-lethal mutant , which has defects in chloroplast development, and found that the mutant phenotype is caused by the suppression of (). Analysis of the heterozygous mutant and -overexpressing transgenic plants indicated that the expression level of is tightly linked to chloroplast development. Characterization of the interaction of pTAC10 with PAPs revealed that pTAC10 interacts with other PAPs, such as FSD2, FSD3, TrxZ, pTAC7, and pTAC14, but it does not interact with PEP core enzymes, such as rpoA and rpoB. Analysis of pTAC10 interactions using truncated pTAC10 proteins showed that the pTAC10 carboxyl-terminal region downstream of the S1 domain is involved in the pTAC10-PAP interaction. Furthermore, overexpression of truncated lacking the C-terminal regions downstream of the S1 domain could not rescue the mutant phenotype and induced an abnormal whitening phenotype in Columbia-0 plants. Our observations suggested that these pTAC10-PAP interactions are essential for the formation of the PEP complex and chloroplast development.

摘要

质体编码 RNA 聚合酶(PEP)对光合基因表达的调控对于叶绿体的发育至关重要。PEP 的活性在很大程度上依赖于植物细胞核基因组中至少编码的 12 种 PEP 相关蛋白(PAPs)。最近提出的一个模型表明,这些 PAPs 通过广泛的 PAP-PEP 或 PAP-PAP 相互作用来调节 PEP 复合物的建立。在这项研究中,我们鉴定了拟南芥()幼苗致死突变体,该突变体在叶绿体发育方面存在缺陷,并发现突变体表型是由()的抑制引起的。对杂合突变体和过表达转基因植物的分析表明,的表达水平与叶绿体发育密切相关。pTAC10 与 PAPs 相互作用的特征表明,pTAC10 与其他 PAPs 相互作用,如 FSD2、FSD3、TrxZ、pTAC7 和 pTAC14,但不与 PEP 核心酶相互作用,如 rpoA 和 rpoB。使用截短的 pTAC10 蛋白分析 pTAC10 相互作用表明,S1 结构域下游的 pTAC10 羧基末端区域参与 pTAC10-PAP 相互作用。此外,过表达缺乏 S1 结构域下游的截短的 不能挽救 突变体表型,并在哥伦比亚-0 植物中诱导异常白化表型。我们的观察结果表明,这些 pTAC10-PAP 相互作用对于 PEP 复合物和叶绿体发育的形成是必不可少的。