Msadek T, Kunst F, Klier A, Rapoport G
Unité de Biochimie Microbienne, Centre National de la Recherche Scientifique URA 1300, Institute Pasteur, Paris, France.
J Bacteriol. 1991 Apr;173(7):2366-77. doi: 10.1128/jb.173.7.2366-2377.1991.
Production of a class of both secreted and intracellular degradative enzymes in Bacillus subtilis is regulated at the transcriptional level by a signal transduction pathway which includes the DegS-DegU two-component system and at least two additional regulatory genes, degQ and degR, encoding polypeptides of 46 and 60 amino acids, respectively. Expression of degQ was shown to be controlled by DegS-DegU. This expression is decreased in the presence of glucose and increased under any of the following conditions: growth with poor carbon sources, amino acid deprivation, phosphate starvation, and growth in the presence of decoyinine, a specific inhibitor of GMP synthetase. In addition, expression of degQ is shown to be positively regulated by the ComP-ComA two-component system. Separate targets for regulation of degQ gene expression by DegS-DegU and ComP-ComA were located by deletion analysis between positions -393 and -186 and between positions -78 and -40, respectively. Regulation of degQ expression by amino acid deprivation was shown to be dependent upon ComA. Regulation by phosphate starvation, catabolite repression, and decoyinine was independent of the two-component systems and shown to involve sequences downstream from position -78. The ComP-ComA and DegS-DegU two-component systems seem to be closely related, sharing several target genes in common, such as late competence genes, as well as the degQ regulatory gene. Sequence analysis of the degQ region revealed the beginning of an open reading frame directly downstream from degQ. Disruption of this gene, designated comQ, suggests that it also controls expression of degQ and is required for development of genetic competence.
枯草芽孢杆菌中一类分泌型和细胞内降解酶的产生在转录水平上受一个信号转导途径调控,该途径包括DegS-DegU双组分系统以及至少两个额外的调控基因degQ和degR,它们分别编码46和60个氨基酸的多肽。已证明degQ的表达受DegS-DegU控制。在葡萄糖存在的情况下这种表达降低,而在以下任何一种条件下增加:以不良碳源生长、氨基酸剥夺、磷酸盐饥饿以及在GMP合成酶的特异性抑制剂脱氧助间型霉素存在下生长。此外,degQ的表达显示受ComP-ComA双组分系统正调控。通过缺失分析分别在-393至-186位和-78至-40位之间定位了DegS-DegU和ComP-ComA对degQ基因表达调控的不同靶标。已证明氨基酸剥夺对degQ表达的调控依赖于ComA。磷酸盐饥饿、分解代谢物阻遏和脱氧助间型霉素的调控独立于双组分系统,且显示涉及-78位下游的序列。ComP-ComA和DegS-DegU双组分系统似乎密切相关,共有几个共同的靶基因,如后期感受态基因以及degQ调控基因。degQ区域的序列分析揭示了degQ直接下游一个开放阅读框的起始。该基因(命名为comQ)的破坏表明它也控制degQ的表达,并且是遗传感受态发育所必需 的。