Liu J D, Parkinson J S
Biology Department, University of Utah, Salt Lake City 84112.
J Bacteriol. 1991 Aug;173(16):4941-51. doi: 10.1128/jb.173.16.4941-4951.1991.
This study presents two lines of genetic evidence consistent with the premise that CheW, a cytoplasmic component of the chemotactic signaling system of Escherichia coli, interacts directly with Tsr, the membrane-bound serine chemoreceptor. (i) We demonstrated phenotypic suppression between 10 missense mutant CheW proteins and six missense mutant Tsr proteins. Most of these mutant proteins had leaky chemotaxis defects and were partially dominant, implying relatively minor functional alterations. Their suppression pattern was allele specific, suggesting that the mutant proteins have compensatory conformational changes at sites of interactive contact. (ii) We isolated five partially dominant CheW mutations and found that four of them were similar or identical to the suppressible CheW mutant proteins. This implies that there are only a few ways in which CheW function can be altered to produce dominant defects and that dominance is mediated through interactions of CheW with Tsr. The amino acid replacements in these mutant proteins were inferred from their DNA sequence changes. The CheW mutations were located in five regularly spaced clusters in the first two-thirds of the protein. The Tsr mutations were located in a highly conserved region in the middle of the cytoplasmic signaling domain. The hydrophobic moments, overall hydrophobicities, and predicted secondary structures of the mutant segments were consistent with the possibility that they are located at the surface of the CheW and Tsr molecules and represent the contact sites between these two proteins.
本研究提供了两条遗传学证据,支持如下前提:CheW作为大肠杆菌趋化信号系统的一种胞质成分,可直接与膜结合丝氨酸化学感受器Tsr相互作用。(i)我们证明了10种错义突变型CheW蛋白与6种错义突变型Tsr蛋白之间存在表型抑制。这些突变蛋白大多具有渗漏性趋化缺陷且部分呈显性,这意味着功能改变相对较小。它们的抑制模式具有等位基因特异性,表明突变蛋白在相互接触位点发生了补偿性构象变化。(ii)我们分离出5种部分显性的CheW突变,发现其中4种与可被抑制的CheW突变蛋白相似或相同。这意味着CheW功能发生改变以产生显性缺陷的方式只有几种,且显性是通过CheW与Tsr的相互作用介导的。这些突变蛋白中的氨基酸替换可根据其DNA序列变化推断出来。CheW突变位于该蛋白前三分之二区域的5个规则间隔的簇中。Tsr突变位于胞质信号结构域中部的一个高度保守区域。突变片段的疏水矩、整体疏水性和预测的二级结构与它们位于CheW和Tsr分子表面并代表这两种蛋白质之间接触位点的可能性一致。