Lakhani S, Khanna N C, Tewari K K
International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi, India.
Plant Mol Biol. 1993 Dec;23(5):963-79. doi: 10.1007/BF00021812.
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.
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。