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大肠杆菌sohA基因的鉴定、克隆及特性分析,htrA(degP)基因缺失表型的一个抑制子

Identification, cloning, and characterization of the Escherichia coli sohA gene, a suppressor of the htrA (degP) null phenotype.

作者信息

Baird L, Georgopoulos C

机构信息

Department of Cellular, Viral and Molecular Biology, University of Utah School of Medicine, Salt Lake City 84132.

出版信息

J Bacteriol. 1990 Mar;172(3):1587-94. doi: 10.1128/jb.172.3.1587-1594.1990.

Abstract

Two extragenic suppressors which allow temperature-sensitive htrA mutant Escherichia coli bacteria to grow at 42 degrees C and simultaneously acquire a cold-sensitive phenotype at 30 degrees C were isolated. The cold-sensitive phenotype exhibited by one of the mutants was used to clone the corresponding wild-type copy of the suppressor gene. This was done through complementation with a mini-mu plasmid E. coli DNA library, by selection for colonies which were no longer cold sensitive, at 30 degrees C. The cloned suppressor gene was shown to complement the cold-sensitive phenotype of both suppressor mutations. It was mapped to 68 min on the E. coli chromosome through hybridization to the Kohara library of overlapping lambda transducing bacteriophages, which covers the entire E. coli chromosome. The complementing gene was further subcloned on an 830-base-pair (bp) DNA fragment. DNA sequencing revealed the presence of an open reading frame (ORF) of 333 bp which could encode a protein of 12,359 Mr. Subcloning of various DNA fragments from within this 830-bp DNA fragment suggests that this ORF is most likely responsible for suppression of the cold-sensitive phenotype of the htrA suppressor bacteria. By using a T7 polymerase system to overproduce plasmid-encoded proteins, a protein of approximately 12,000 Mr was produced by this cloned DNA fragment. This ORF defines a previously undiscovered gene in E. coli, called sohA (suppressor of htrA).

摘要

分离出了两种基因外抑制子,它们能使温度敏感型htrA突变大肠杆菌在42℃生长,同时在30℃获得冷敏感表型。利用其中一个突变体所表现出的冷敏感表型来克隆抑制基因的相应野生型拷贝。这是通过用一个mini-mu质粒大肠杆菌DNA文库进行互补来完成的,在30℃下选择不再冷敏感的菌落。所克隆的抑制基因被证明能互补两种抑制突变的冷敏感表型。通过与覆盖整个大肠杆菌染色体的重叠λ转导噬菌体的Kohara文库杂交,将其定位到大肠杆菌染色体的68分钟处。互补基因进一步亚克隆到一个830碱基对(bp)的DNA片段上。DNA测序显示存在一个333 bp的开放阅读框(ORF),它可以编码一个12359 Mr的蛋白质。从这个830 bp DNA片段内亚克隆各种DNA片段表明,这个ORF最有可能负责抑制htrA抑制细菌的冷敏感表型。通过使用T7聚合酶系统过量表达质粒编码的蛋白质,这个克隆的DNA片段产生了一个约12000 Mr的蛋白质。这个ORF定义了大肠杆菌中一个以前未被发现的基因,称为sohA(htrA的抑制子)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c93a/208636/869828577e99/jbacter01045-0436-a.jpg

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