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豌豆叶绿体转录活性染色体的新生转录本结合蛋白

Nascent transcript-binding protein of the pea chloroplast transcriptionally active chromosome.

作者信息

Lakhani S, Khanna N C, Tewari K K

机构信息

International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi, India.

出版信息

Plant Mol Biol. 1993 Dec;23(5):963-79. doi: 10.1007/BF00021812.

DOI:10.1007/BF00021812
PMID:8260634
Abstract

This study describes the nascent RNA-binding protein of the pea chloroplast transcriptional complex. The protein has been identified by photoaffinity labelling of the transcriptionally active chromosome (TAC) which utilizes the endogenous plastid DNA as template. UV irradiation of lysed chloroplast or the isolated TAC under conditions optimized for transcription photocross-links nascent radiolabelled transcripts (up to 250 nucleotides in length) to a 48 kDa protein. The photoaffinity labelling of the transcript-binding protein is dependent on UV irradiation, is maximal after about 30 min of irradiation, and is completely dependent on transcriptional activity; no cross-linkage has been observed with pre-synthesized RNA. Cross-linkage is influenced by salts and inhibitors in accordance with their effects on transcription. The photoconjugate is composed of protein and RNA moieties, and can be hydrolysed by several proteases. However, the cross-linked transcript is protected from nucleases until the protein is removed. Manganese enhances photoaffinity labelling of the transcript-binding protein, and this is paralleled by an increase in total transcriptional activity of TAC. This protein was isolated by 2-dimensional polyacrylamide gel electrophoresis and the sequence of 15 amino acid residues at the amino terminus was determined. The nascent transcript-binding protein appears to be involved in the transcription of all three classes of chloroplast genes. We also found a polypeptide of identical molecular weight to get cross-linked to nascent transcripts in chloroplasts isolated from other legumes such as Cicer arietenum, Vigna radiata and Phaseolus vulgaris, and monocots like Zea mays, Oryza sativa and Pennisetum americanum.

摘要

本研究描述了豌豆叶绿体转录复合体的新生RNA结合蛋白。该蛋白已通过对转录活性染色体(TAC)进行光亲和标记鉴定,TAC以叶绿体内源DNA为模板。在为转录优化的条件下,对裂解的叶绿体或分离的TAC进行紫外线照射,可使新生的放射性标记转录本(长度达250个核苷酸)与一种48 kDa的蛋白发生光交联。转录本结合蛋白的光亲和标记依赖于紫外线照射,照射约30分钟后达到最大值,且完全依赖于转录活性;未观察到与预合成RNA的交联。交联受盐和抑制剂的影响,这与它们对转录的影响一致。光共轭物由蛋白质和RNA部分组成,可被几种蛋白酶水解。然而,在蛋白质被去除之前,交联的转录本可免受核酸酶的作用。锰增强了转录本结合蛋白的光亲和标记,同时TAC的总转录活性也增加。通过二维聚丙烯酰胺凝胶电泳分离出该蛋白,并测定了其氨基末端15个氨基酸残基的序列。新生转录本结合蛋白似乎参与了叶绿体所有三类基因的转录。我们还发现,在从其他豆科植物如鹰嘴豆、绿豆和菜豆以及单子叶植物如玉米、水稻和美洲狼尾草分离的叶绿体中,一种分子量相同的多肽也能与新生转录本发生交联。

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1
Nascent transcript-binding protein of the pea chloroplast transcriptionally active chromosome.豌豆叶绿体转录活性染色体的新生转录本结合蛋白
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Photoaffinity labelling of the pea chloroplast transcriptional complex by nascent RNA in vitro.豌豆叶绿体转录复合物在体外被新生RNA进行光亲和标记。
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Identification of the template binding polypeptide in the pea chloroplast transcriptional complex.豌豆叶绿体转录复合物中模板结合多肽的鉴定
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Three types of nuclear genes encoding chloroplast RNA-binding proteins (cp29, cp31 and cp33) are present in Arabidopsis thaliana: presence of cp31 in chloroplasts and its homologue in nuclei/cytoplasms.拟南芥中存在三种编码叶绿体RNA结合蛋白(cp29、cp31和cp33)的核基因:叶绿体中存在cp31及其在细胞核/细胞质中的同源物。
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A plastid protein NUS1 is essential for build-up of the genetic system for early chloroplast development under cold stress conditions.冷胁迫条件下,质体蛋白 NUS1 对于早期叶绿体发育的遗传系统的建立是必需的。
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An open reading frame encoding a putative haem-binding polypeptide is cotranscribed with the pea chloroplast gene for apocytochrome f.一个编码假定的血红素结合多肽的开放阅读框与豌豆叶绿体脱辅基细胞色素f基因共转录。
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Environmental stress-mediated differential 3' end formation of chloroplast RNA-binding protein transcripts.环境胁迫介导的叶绿体RNA结合蛋白转录本3'端形成差异
Plant Mol Biol. 1994 Nov;26(3):833-49. doi: 10.1007/BF00028852.

引用本文的文献

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Whirly1 in chloroplasts associates with intron containing RNAs and rarely co-localizes with nucleoids.叶绿体内的 Whirly1 与含有内含子的 RNA 结合,很少与核体共定位。
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本文引用的文献

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Specific in vitro transcription of 16S rRNA gene by pea chloroplast RNA polymerase.豌豆叶绿体 RNA 聚合酶对 16S rRNA 基因的特异性体外转录。
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Polypeptides of DNA-dependent RNA polymerase of spinach chloroplasts: characterization by antibody-linked polymerase assay and determination of sites of synthesis.
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