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信号序列突变的新型抑制因子prlG与大肠杆菌的secE基因紧密连锁。

New suppressors of signal-sequence mutations, prlG, are linked tightly to the secE gene of Escherichia coli.

作者信息

Stader J, Gansheroff L J, Silhavy T J

机构信息

Department of Biology, Princeton University, New Jersey 08544.

出版信息

Genes Dev. 1989 Jul;3(7):1045-52. doi: 10.1101/gad.3.7.1045.

Abstract

Analysis of more than 100 extragenic suppressors of the lamB14D signal-sequence mutation (changes Val in the hydrophobic core region at position 14 to Asp) has revealed alterations that appear to lie at prlA (secY) and secA (prlD), two loci known to be mutable to suppressor alleles, and a new suppressor termed prlG. One allele of the new suppressor class, prlG1, has been characterized in some detail. This suppressor counteracts, to some degree, the export defect conferred by a variety of signal-sequence mutations in two different genes, lamB and malE. Genetic analysis shows that the dominant suppressor mutations are linked tightly to, and probably allelic with, the gene secE. This result, coupled with data obtained with conditional-lethal alleles of secE, argues strongly that SecE is an important component of the cellular protein export machinery in Escherichia coli.

摘要

对超过100个lamB14D信号序列突变(将第14位疏水核心区域的缬氨酸变为天冬氨酸)的基因外抑制子进行分析,发现了一些改变,这些改变似乎位于prlA(secY)和secA(prlD),这两个已知可突变为抑制子等位基因的位点,以及一个名为prlG的新抑制子。新抑制子类别的一个等位基因prlG1已得到一定程度的详细表征。这种抑制子在一定程度上抵消了由lamB和malE这两个不同基因中的多种信号序列突变所导致的输出缺陷。遗传分析表明,显性抑制子突变与secE基因紧密连锁,并且可能与其等位。这一结果,再加上从secE的条件致死等位基因获得的数据,有力地表明SecE是大肠杆菌细胞蛋白质输出机制的一个重要组成部分。

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