Tyagi J S, Tyagi A K, Bhargava S
Department of Biotechnology, All India Institute of Medical Sciences, New Delhi.
Trop Med Parasitol. 1990 Sep;41(3):294-6.
DNAs from nine mycobacterial species were cleaved with different restriction endonucleases and hybridized with cDNA probes synthesized to total transfer RNAs (tRNAs) from Mycobacterium smegmatis and M. tuberculosis. The hybridization data indicate that tRNA genes are conserved but their gross genomic organization has diverged in six of the nine species examined. Species of the MTB complex appeared to have identical tRNA gene organization. Hybridization with cDNAs synthesized to 23S plus 16S rRNAs from Escherichia coli indicate that the tRNA genes map near the rRNA genes. Recombinant plasmids, pSB1, pSB2, pSB4 and pSB8 encoding tRNA(s) and rRNA(s) were isolated from a gene bank of M. tuberculosis H37Rv. Using pSB2 as probe, a SalI RFLP was observed that distinguishes the virulent and avirulent strains of M. tuberculosis H37Rv and H37Ra, respectively.
用不同的限制性内切酶切割来自9种分枝杆菌的DNA,并与针对耻垢分枝杆菌和结核分枝杆菌的总转移RNA(tRNA)合成的cDNA探针杂交。杂交数据表明,tRNA基因是保守的,但在9个被检测物种中的6个物种中,它们的总体基因组组织已经发生了分化。结核分枝杆菌复合群的物种似乎具有相同的tRNA基因组织。与针对大肠杆菌23S加16S rRNA合成的cDNA杂交表明,tRNA基因定位于rRNA基因附近。从结核分枝杆菌H37Rv的基因文库中分离出编码tRNA和rRNA的重组质粒pSB1、pSB2、pSB4和pSB8。以pSB2为探针,观察到一种SalI限制性片段长度多态性(RFLP),它分别区分了结核分枝杆菌H37Rv和H37Ra的有毒和无毒菌株。