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鼠伤寒沙门氏菌组氨酸转运操纵子的hisM基因中的一个突变热点是由于重复序列的缺失,导致转运特异性改变。

A mutational hot-spot in the hisM gene of the histidine transport operon in Salmonella typhimurium is due to deletion of repeated sequences and results in an altered specificity of transport.

作者信息

Payne G M, Spudich E N, Ames G F

出版信息

Mol Gen Genet. 1985;200(3):493-6. doi: 10.1007/BF00425737.

Abstract

Duplicated sequences within hisM, a gene coding for a membrane-bound component of histidine transport, result in frequent deletions which, being in frame, allow production of an altered protein with apparent changed specificity of transport. While the wild-type transport system does not transport L-histidinol but does transport L-histidine and several of its analogs, the hisM deletion mutants do not transport the latter compounds but do transport L-histidinol. These results are interpreted as supporting the hypothesis (Ames and Higgins 1983) that transport through periplasmic systems involves binding of the substrate by the cytoplasmic membrane-bound components.

摘要

hisM基因编码组氨酸转运的膜结合成分,其内部的重复序列会导致频繁缺失,这些缺失保持读码框,使得能够产生一种转运特异性明显改变的变异蛋白。野生型转运系统不转运L-组氨醇,但能转运L-组氨酸及其几种类似物,而hisM缺失突变体不转运后几种化合物,但能转运L-组氨醇。这些结果被解释为支持如下假说(Ames和Higgins,1983年):通过周质系统的转运涉及细胞质膜结合成分与底物的结合。

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