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结核分枝杆菌强毒株中差异表达基因的鉴定与克隆

Identification and cloning of genes differentially expressed in the virulent strain of Mycobacterium tuberculosis.

作者信息

Kinger A K, Tyagi J S

机构信息

Department of Biotechnology, All India Institute of Medical Sciences, New Delhi.

出版信息

Gene. 1993 Sep 6;131(1):113-7. doi: 10.1016/0378-1119(93)90678-v.

Abstract

The mechanism(s) used by Mycobacterium tuberculosis to establish disease in the human host are not well understood. The virulent M. tuberculosis H37Rv strain and its avirulent derivative M. tuberculosis H37Ra provide an attractive system for the identification of virulence-specific genes of the tubercle bacillus. Differentially expressed genes in the virulent strain of M. tuberculosis (dev genes) were identified by screening a plasmid gene bank of H37Rv with a cDNA probe that was enriched in dev transcripts by subtraction of RNAs common to H37Ra. Individual dev clones coded for RNA transcripts that were differentially expressed in H37Rv in comparison to H37Ra. In contrast, mRNAs and stable RNAs that were commonly expressed in both the strains were present in equivalent amounts. The identification and cloning of dev genes marks the first step in defining bacterial gene(s) involved in the pathogenesis of M. tuberculosis.

摘要

结核分枝杆菌在人类宿主中引发疾病的机制尚未完全明确。有毒力的结核分枝杆菌H37Rv菌株及其无毒力衍生物结核分枝杆菌H37Ra为鉴定结核杆菌的毒力特异性基因提供了一个有吸引力的系统。通过用一个cDNA探针筛选H37Rv的质粒基因文库来鉴定结核分枝杆菌有毒力菌株中的差异表达基因(dev基因),该cDNA探针通过减去H37Ra共有的RNA而富集了dev转录本。与H37Ra相比,各个dev克隆编码的RNA转录本在H37Rv中差异表达。相反,两种菌株中共同表达的mRNA和稳定RNA的量相当。dev基因的鉴定和克隆标志着确定参与结核分枝杆菌发病机制的细菌基因的第一步。

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