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首页> 外文期刊>Journal of bacteriology >Organization of rRNA genes in Mycobacterium bovis BCG.
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Organization of rRNA genes in Mycobacterium bovis BCG.

机译:牛分枝杆菌BCG中rRNA基因的组织。

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摘要

The number of rRNA genes in Mycobacterium bovis BCG was examined by Southern hybridization of end-labeled 5S, 16S, and 23S rRNAs with BamHI, PstI, and SalI digests of M. bovis BCG DNA. Each RNA probe gave only one radioactive band with three kinds of DNA digest. These results suggest that M. bovis BCG chromosomes may carry only a minimum set of rRNA genes. Hybridization of randomly labeled rRNAs with BamHI, PstI, SalI, BglII, and PvuII digests of DNA from the same organism supported these conclusions. The 6.4-kilobase-pair SalI fragment containing the entire structural genes for both 16S and 23S rRNAs was cloned into pBR322. The cloned fragment was characterized by restriction endonuclease mapping, DNA-RNA hybridization analysis, and the R-loop technique. The results indicated that the fragments contained rRNA genes in the following order: 16S, 23S, and 5S rRNA genes. No tRNA gene was detected in the spacer region between the 16S and 23S rRNA genes, but one was found downstream of the 23S rRNA and 5S rRNA genes.
机译:通过末端标记的5S,16S和23S rRNA与牛分枝杆菌BCG DNA的BamHI,PstI和SalI消化物的Southern杂交来检测牛分枝杆菌BCG中rRNA基因的数目。每个RNA探针仅给出一个带有3种DNA消化的放射性带。这些结果表明,牛分枝杆菌BCG染色体可能仅携带最少的rRNA基因集。随机标记的rRNA与来自同一生物体的DNA的BamHI,PstI,SalI,BglII和PvuII消化物的杂交支持了这些结论。将包含16S和23S rRNA完整结构基因的6.4碱基对SalI片段克隆到pBR322中。通过限制性核酸内切酶作图,DNA-RNA杂交分析和R环技术对克隆的片段进行了表征。结果表明,这些片段按以下顺序包含rRNA基因:16S,23S和5S rRNA基因。在16S和23S rRNA基因之间的间隔区中未检测到tRNA基因,但在23S rRNA和5S rRNA基因的下游发现了一个tRNA基因。

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