Rhie H G, Shimkets L J
Department of Microbiology, University of Georgia, Athens 30602.
J Bacteriol. 1991 Apr;173(7):2206-11. doi: 10.1128/jb.173.7.2206-2211.1991.
The csgA gene encodes an extracellular protein that plays an essential role in the regulation of fruiting-body formation and sporulation of Myxococcus xanthus. The csgA suppressor allele soc-500 (formerly referred to as csp-500) was selected based on its ability to restore sporulation to csgA cells under developmental conditions at 32 degrees C. The soc-500 allele was subsequently found to induce sporulation of csgA+ or csgA cells simply by shifting the temperature of vegetatively growing cells to 15 degrees C. Low-temperature-induced sporulation of soc-500 strains occurred in the absence of two requirements for fruiting-body sporulation: low nutrient levels and a high temperature. Low temperature alone caused the expression of many developmentally regulated genes but did not support the development of wild-type cells. The soc-500 allele appears to activate genes involved with sensing nutritional stress. At low temperature on a nutritionally rich medium, soc-500 induced expression of the tps gene which is normally expressed following nutritional shiftdown. The soc-500 allele was cloned and integrated into the wild-type chromosome by site-specific recombination. It was dominant over the wild-type allele in merodiploids and is contained on a 3-kbp DraI-ClaI restriction fragment. The soc-500 transcriptional unit spans a 300-bp PstI-PstI restriction fragment, since deletion of the PstI restriction fragment inhibits both csgA suppression and low-temperature induction. These results suggest that the soc-500 mutation lies in a gene that is involved in nutrient sensing.
csgA基因编码一种细胞外蛋白,该蛋白在黄色粘球菌子实体形成和孢子形成的调控中起着至关重要的作用。csgA抑制等位基因soc - 500(以前称为csp - 500)是根据其在32摄氏度的发育条件下恢复csgA细胞孢子形成的能力而选择的。随后发现,soc - 500等位基因只需将营养生长细胞的温度转移到15摄氏度,就能诱导csgA +或csgA细胞的孢子形成。soc - 500菌株的低温诱导孢子形成发生在子实体孢子形成的两个条件缺失的情况下:低营养水平和高温。仅低温就会导致许多发育调控基因的表达,但不支持野生型细胞的发育。soc - 500等位基因似乎激活了与感知营养应激相关的基因。在营养丰富的培养基上低温培养时,soc - 500诱导了tps基因的表达,该基因通常在营养物质减少后表达。soc - 500等位基因通过位点特异性重组被克隆并整合到野生型染色体中。在部分二倍体中,它对野生型等位基因呈显性,并且位于一个3kbp的DraI - ClaI限制片段上。soc - 500转录单元跨越一个300bp的PstI - PstI限制片段,因为删除PstI限制片段会抑制csgA抑制和低温诱导。这些结果表明,soc - 500突变存在于一个参与营养感知作用的基因中。