Yano R, Yura T
Institute for Virus Research, Kyoto University, Japan.
J Bacteriol. 1989 Mar;171(3):1712-7. doi: 10.1128/jb.171.3.1712-1717.1989.
Several suppressors (suhD) that can specifically suppress the temperature-sensitive opal rpoH11 mutation of Escherichia coli K-12 have been isolated and characterized. Unlike the parental rpoH11 mutant deficient in the heat shock response, the temperature-resistant pseudorevertants carrying suhD were capable of synthesizing sigma 32 and exhibiting partial induction of heat shock proteins. These strains were also cold sensitive and unable to grow at 25 degrees C. Genetic mapping and complementation studies permitted us to localize suhD near rpsO (69 min), the structural gene for ribosomal protein S15. Ribosomes and polyribosomes prepared from suhD cells contained a reduced level (ca. 10%) of S15 relative to that of the wild type. Cloning and sequencing of suhD revealed that an IS10-like element had been inserted at the attenuator-terminator region immediately downstream of the rpsO coding region. The rpsO mRNA level in the suhD strain was also reduced to about 10% that of wild type. Apparently, ribosomes lacking S15 can actively participate in protein synthesis and suppress the rpoH11 opal (UGA) mutation at high temperature but cannot sustain cell growth at low temperature.
已经分离并鉴定了几种能够特异性抑制大肠杆菌K-12温度敏感型乳白密码子rpoH11突变的抑制子(suhD)。与缺乏热休克反应的亲本rpoH11突变体不同,携带suhD的耐温假回复体能够合成σ32并表现出热休克蛋白的部分诱导。这些菌株对冷敏感,无法在25℃下生长。遗传图谱绘制和互补研究使我们能够将suhD定位在rpsO(69分钟)附近,rpsO是核糖体蛋白S15的结构基因。相对于野生型,从suhD细胞制备的核糖体和多核糖体中S15的含量降低(约10%)。suhD的克隆和测序表明,一个类似IS10的元件已插入到rpsO编码区下游紧邻的衰减子-终止子区域。suhD菌株中rpsO mRNA水平也降至野生型的约10%。显然,缺乏S15的核糖体能够在高温下积极参与蛋白质合成并抑制rpoH11乳白密码子(UGA)突变,但在低温下无法维持细胞生长。