首页> 美国卫生研究院文献>Journal of Bacteriology >New minC mutations suggest different interactions of the same region of division inhibitor MinC with proteins specific for minD and dicB coinhibition pathways.
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New minC mutations suggest different interactions of the same region of division inhibitor MinC with proteins specific for minD and dicB coinhibition pathways.

机译:新的minC突变表明分裂抑制剂MinC的同一区域与对minD和dicB共抑制途径具有特异性的蛋白质的相互作用不同。

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摘要

Proper positioning of division sites in Escherichia coli requires balanced expression of minC, minD, and minE gene products. Previous genetic analysis has shown that either MinD or an apparently unrelated protein, DicB, cooperates with MinC to inhibit division. We have isolated and sequenced minC mutations that suppress division inhibition caused by overproduction of either DicB or MinD proteins. Most missense mutations were located in the amino acid 160 to 200 region of MinC (231 amino acids). Some mutations exhibited preferential resistance to one or the other coinhibitor, suggesting that two distinct proteins, possibly MinD and DicB themselves, interact in slightly different manners with the same region of MinC to promote division inhibition.
机译:大肠杆菌中分裂位点的正确定位需要minC,minD和minE基因产物的平衡表达。先前的遗传分析表明,MinD或表面上无关的蛋白质DicB与MinC协同抑制分裂。我们已经分离和测序了minC突变,这些突变可抑制由DicB或MinD蛋白的过量生产引起的分裂抑制。大多数错义突变位于MinC的160至200个氨基酸区域(231个氨基酸)。一些突变显示出对一种或另一种共抑制物的优先抗性,表明两种不同的蛋白质,可能是MinD和DicB本身,与MinC的同一区域相互作用的方式略有不同,从而促进了分裂抑制。

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