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结核分枝杆菌核糖体RNA操纵子的启动子、16S rRNA和间隔区的核苷酸序列及其与麻风分枝杆菌前体rRNA的比较。

The nucleotide sequence of the promoter, 16S rRNA and spacer region of the ribosomal RNA operon of Mycobacterium tuberculosis and comparison with Mycobacterium leprae precursor rRNA.

作者信息

Kempsell K E, Ji Y E, Estrada I C, Colston M J, Cox R A

机构信息

Laboratory of Developmental Biochemistry, National Institute for Medical Research, Mill Hill, London, UK.

出版信息

J Gen Microbiol. 1992 Aug;138 Pt 8:1717-27. doi: 10.1099/00221287-138-8-1717.

Abstract

Mycobacterium tuberculosis H37Rv has a single rrn (ribosomal RNA) operon. The operon was cloned and a region of 1536 nucleotides was sequenced, starting 621 bp upstream from the 5'-end of the 16S rRNA coding region and continuing to the start of the 23S rRNA coding region. The 16S rRNA sequence inferred from the gene sequence was found to differ in one position from Mycobacterium bovis (nucleotide 1443) and from Mycobacterium microti (nucleotide 427). A single putative promoter was identified on the basis of similarities with the sequence of rrn operons of Bacillus subtilis and Escherichia coli. The regions of similarity include a -35 box, a -10 box, a stringent response element, antitermination signals, potential RNAase III processing sites and features of precursor rRNA secondary structure. Sequences upstream from the 5'-end of Mycobacterium leprae 16S rRNA were also investigated. Homologous schemes of secondary structure were deduced for precursor rRNA of both M. tuberculosis and M. leprae; although the principal features are common to both species there are notable differences.

摘要

结核分枝杆菌H37Rv有一个单一的rrn(核糖体RNA)操纵子。该操纵子被克隆,并对一个1536个核苷酸的区域进行了测序,从16S rRNA编码区5'端上游621 bp处开始,一直延伸到23S rRNA编码区的起始处。从基因序列推断出的16S rRNA序列在一个位置上与牛分枝杆菌(核苷酸1443)和微小分枝杆菌(核苷酸427)不同。基于与枯草芽孢杆菌和大肠杆菌rrn操纵子序列的相似性,鉴定出一个单一的假定启动子。相似区域包括一个-35框、一个-10框、一个严谨反应元件、抗终止信号、潜在的RNAase III加工位点以及前体rRNA二级结构的特征。还研究了麻风分枝杆菌16S rRNA 5'端上游的序列。推导了结核分枝杆菌和麻风分枝杆菌前体rRNA的同源二级结构方案;尽管两个物种的主要特征相同,但也存在显著差异。

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