colcolcolor链霉菌A3多基因区域的鉴定与鉴定(2)。

A Burger, K Sichler, G Kelemen, M Buttner, W Wohlleben
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引用次数: 37

摘要

在对colcololstreptomyces coelicolor A3(2)中新的分化因子的研究中,在S. coelicolor图谱的11点钟位置发现了一个位点,其中包含几个与大肠杆菌和枯草芽孢杆菌的细胞分裂和分化基因广泛相似的基因。序列数据表明,该区域含有mreb、mreC、mreD(鼠蛋白形成基因簇E)、pbp83(高分子量青霉素结合蛋白)和sfr (spoVE/ftsW/rodA家族成员)基因。据报道,大肠杆菌和芽孢杆菌中有更多的基因产物决定细胞形状。coelicolor mreC基因因基因破坏而失活,导致突变体与野生型相比表现出明显的生长迟缓。mreB基因的失活与生存能力不相容,因此mreB代表链霉菌细胞分裂基因,是生存所必需的。启动子探针实验鉴定出一个操纵子结构,启动子位于mreB、pbp83和sfr的上游。对mreB转录的详细研究揭示了三个启动子的存在;其中两个是本构转录的,而第三个是发育调控的。
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Identification and characterization of the mre gene region of Streptomyces coelicolor A3(2).

During a search for new differentiation factors in Streptomyces coelicolor A3(2), a locus at 11 o'clock on the S. coelicolor map was identified which harbours several genes that show extensive similarity to cell division and differentiation genes from Escherichia coli and Bacillus subtilis. From the sequence data it was concluded that the region contains the genes mireB, mreC, mreD (murein formation gene cluster E), pbp83 (high-molecular-weight penicillin-binding protein) and sfr (member of the spoVE/ftsW/rodA family). Mre gene products are reported to be responsible for determining cell shape in E. coli and Bacillus. The S. coelicolor mreC gene was inactivated by gene disruption, resulting in mutants which showed significant growth retardation in comparison to the wild type. Inactivation of the mreB gene was incompatible with viability, and thus mreB represents a Streptomyces cell division gene that is essential for survival. Promoter-probe experiments led to the identification of an operon structure, with promoters located upstream of mreB, pbp83 and sfr. Detailed studies of mreB transcription revealed the existence of three promoters; two of them are constitutively transcribed, whereas the third is developmentally regulated.

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