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允许黄色粘球菌中不依赖A信号进行发育基因表达的抑制因子。

Suppressors that permit A-signal-independent developmental gene expression in Myxococcus xanthus.

作者信息

Kaplan H B, Kuspa A, Kaiser D

机构信息

Department of Biochemistry, Stanford University School of Medicine, California 94305.

出版信息

J Bacteriol. 1991 Feb;173(4):1460-70. doi: 10.1128/jb.173.4.1460-1470.1991.

Abstract

Progression through the early stages of Myxococcus xanthus fruiting body development requires the cell-to-cell transmission of soluble material called A signal. During these early stages, expression from the gene identified by Tn5 lac insertion omega 4521 increases. A DNA probe of the omega 4521 gene was constructed. Use of this probe showed that accumulation of mRNA corresponding to the omega 4521 gene depends upon A signal. A-signal-deficient (asg) mutants fail to accumulate this RNA, and the external addition of A signal restores accumulation. To identify links between A signal and its responsive gene, omega 4521, suppressors of an asg mutation were generated. All of the suppressor alleles restored lacZ expression from omega 4521 in the absence of A signal, and they were demonstrated to be neither reversions of the asgB mutation nor mutations in the promoter of omega 4521. Fifteen suppressor mutations map to two loci, sasA and sasB (for suppressor of asg). sasA and sasB mutants differ phenotypically during growth and development. Mid-logarithmic-phase sasA asgB double mutants, like sas+ asg+ strains, express low levels of lacZ, whereas sasB asgB double mutants express high levels. sasA asg+ mutants form abnormal colonies, are less cohesive than wild type, and are defective in fruiting body formation and sporulation. In contrast, sasB asg+ mutants form normal colonies, are as cohesive as wild type, and appear to develop normally. The characteristics of sasA suppressors implicate the sasA+ product as a negative regulator in the A-signal-dependent regulation of omega 4521.

摘要

黄色粘球菌子实体发育早期阶段的进展需要一种名为A信号的可溶性物质进行细胞间传递。在这些早期阶段,由Tn5 lac插入突变体omega 4521鉴定出的基因表达增加。构建了omega 4521基因的DNA探针。使用该探针表明,与omega 4521基因相对应的mRNA积累依赖于A信号。A信号缺陷(asg)突变体无法积累这种RNA,而外部添加A信号可恢复积累。为了确定A信号与其响应基因omega 4521之间的联系,产生了asg突变的抑制子。所有抑制子等位基因在没有A信号的情况下恢复了omega 4521的lacZ表达,并且证明它们既不是asgB突变的回复突变,也不是omega 4521启动子中的突变。15个抑制子突变定位于两个位点,sasA和sasB(asg的抑制子)。sasA和sasB突变体在生长和发育过程中表现出不同的表型。对数中期的sasA asgB双突变体,如sas+ asg+菌株,表达低水平的lacZ,而sasB asgB双突变体表达高水平。sasA asg+突变体形成异常菌落,比野生型的凝聚力小,并且在子实体形成和孢子形成方面存在缺陷。相比之下,sasB asg+突变体形成正常菌落,与野生型的凝聚力相同,并且似乎发育正常。sasA抑制子的特征表明sasA+产物是omega 4521的A信号依赖性调节中的负调节因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c6a/207283/8cb7fb2e3315/jbacter00094-0106-a.jpg

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