Lipinska B, Sharma S, Georgopoulos C
Department of Cellular, Viral and Molecular Biology, University of Utah Medical Center, Salt Lake City 84132.
Nucleic Acids Res. 1988 Nov 11;16(21):10053-67. doi: 10.1093/nar/16.21.10053.
Previous work has established that the E. coli htrA gene product is essential for bacterial survival at temperatures above 42 degrees. We have sequenced the htrA gene region and found an open reading frame (ORF) coding for a protein of 491 amino acids with a calculated molecular weight of 51,163 daltons. This molecular weight corresponds well with that seen following electrophoresis on SDS-polyacrylamide gels. This protein has an amino-terminal sequence typical for a leader peptide and undergoes post-translational modification by cleavage of an amino-terminal portion. The insertional mutations which affect the function of the htrA gene map inside this ORF. The levels of htrA mRNA increase rapidly and transiently upon heat shock in a manner independent of the rpoH gene, which encodes the sigma 32 RNA polymerase subunit and is known to regulate transcription of typical heat shock genes. Using S1 mapping and RNA primer extension, we have identified the htrA promoter and found that it is similar to the P3 promoter of the rpoH gene. The P3 promoter is especially active at high temperatures and is recognized by a recently identified transcriptional factor, sigma E.
先前的研究已经证实,大肠杆菌htrA基因产物对于细菌在42摄氏度以上温度下的存活至关重要。我们对htrA基因区域进行了测序,发现一个开放阅读框(ORF),其编码一个由491个氨基酸组成的蛋白质,计算分子量为51,163道尔顿。这个分子量与在SDS-聚丙烯酰胺凝胶上电泳后观察到的分子量非常吻合。该蛋白质具有典型的前导肽氨基末端序列,并通过氨基末端部分的切割进行翻译后修饰。影响htrA基因功能的插入突变定位在这个ORF内部。htrA mRNA的水平在热休克后迅速且短暂地增加,其方式独立于rpoH基因,rpoH基因编码σ32 RNA聚合酶亚基,已知可调节典型热休克基因的转录。使用S1作图和RNA引物延伸,我们鉴定了htrA启动子,发现它与rpoH基因的P3启动子相似。P3启动子在高温下特别活跃,并被最近鉴定的转录因子σE识别。