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Characterization of the dnaG Locus in Mycobacterium smegmatis Reveals Linkage of DNA Replication and Cell Division

机译:耻垢分枝杆菌中dnaG基因座的特征揭示了DNA复制和细胞分裂的联系。

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摘要

We have isolated a UV-induced temperature-sensitive mutant of Mycobacterium smegmatis that fails to grow at 42°C and exhibits a filamentous phenotype following incubation at the nonpermissive temperature, reminiscent of a defect in cell division. Complementation of this mutant with an M. smegmatis genomic library and subsequent subcloning reveal that the defect lies within the M. smegmatis dnaG gene encoding DNA primase. Sequence analysis of the mutant dnaG allele reveals a substitution of proline for alanine at position 496. Thus, dnaG is an essential gene in M. smegmatis, and DNA replication and cell division are coupled processes in this species. Characterization of the sequences flanking the M. smegmatis dnaG gene shows that it is not part of the highly conserved macromolecular synthesis operon present in other eubacterial species but is part of an operon with a dgt gene encoding dGTPase. The organization of this operon is conserved in Mycobacterium tuberculosis and Mycobacterium leprae, suggesting that regulation of DNA replication, transcription, and translation may be coordinated differently in the mycobacteria than in other bacteria.
机译:我们已经分离出紫外线诱导的耻垢分枝杆菌的温度敏感突变体,该突变体无法在42°C下生长,并且在非容许温度下孵育后表现出丝状表型,令人联想到细胞分裂的缺陷。该突变体与耻垢分枝杆菌基因组文库的互补和随后的亚克隆揭示该缺陷位于编码DNA primase的耻垢分枝杆菌dnaG基因内。突变dnaG等位基因的序列分析揭示了脯氨酸在496位上被丙氨酸取代。因此,dnaG是耻垢分枝杆菌中必不可少的基因,DNA复制和细胞分裂是该物种中的耦合过程。耻垢分枝杆菌dnaG基因两侧序列的特征表明,它不是存在于其他真细菌物种中的高度保守的大分子合成操纵子的一部分,而是具有编码dGTPase的dgt基因的操纵子的一部分。该操纵子的组织在结核分枝杆菌和麻风分枝杆菌中是保守的,这表明在分枝杆菌中与其他细菌相比,DNA复制,转录和翻译的调控可能有所不同。

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