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马克斯·普朗克分子遗传学研究所,维特曼部门,柏林-达勒姆,德意志联邦共和国。

Max-Planck-Institut für Molekulare Genetik, Abteilung Wittmann, Berlin-Dahlem, GFR.

作者信息

Zwieb C, Brimacombe R

出版信息

Nucleic Acids Res. 1979;6(5):1775-90. doi: 10.1093/nar/6.5.1775.

Abstract

It is well established that when E. coli 30S ribosomal subunits are irradiated with ultraviolet light under mild conditions a specific cross-link is formed between protein S7 and the 16S RNA. Methodology is presented for the analysis of the single nucleotide residue concerned in this cross-link. Firstly, the identity of the ribonuclease T1 octanucleotide attached to S7 is confirmed by a new method, which involves isolation and analysis of S7-polynucleotide complexes containing 30 -- 40 nucleotides. Secondly, the isolated S7-octanucleotide complex is digested successively with ribonuclease A, proteinase K and ribonuclease T2, and the nucleotides liberated are identified. The results show unambiguously that uridine residue number 1239 in the 16S RNA sequence is cross-linked to protein S7.

摘要

众所周知,在温和条件下用紫外线照射大肠杆菌30S核糖体亚基时,蛋白质S7与16S RNA之间会形成一种特定的交联。本文介绍了分析这种交联中相关单核苷酸残基的方法。首先,通过一种新方法确定了与S7相连的核糖核酸酶T1八核苷酸的身份,该方法涉及分离和分析含有30 - 40个核苷酸的S7 - 多核苷酸复合物。其次,将分离出的S7 - 八核苷酸复合物依次用核糖核酸酶A、蛋白酶K和核糖核酸酶T2消化,并鉴定释放出的核苷酸。结果明确表明,16S RNA序列中的第1239位尿苷残基与蛋白质S7交联。

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