Binnie C, Lampe M, Losick R
Proc Natl Acad Sci U S A. 1986 Aug;83(16):5943-7. doi: 10.1073/pnas.83.16.5943.
sigma 37 is a minor species of RNA polymerase sigma factor found in the Gram-positive bacterium Bacillus subtilis. sigma 37 governs the transcription in vitro of genes that are turned on at an early stage in spore formation, as well as other genes that are switched on at the end of the exponential phase of growth but that are not under sporulation control. To study the role of sigma 37 in B. subtilis gene expression, we have cloned the gene for this minor species of sigma factor in Escherichia coli by using as a hybridization probe a synthetic oligonucleotide that was designed on the basis of the NH2-terminal amino acid sequence of sigma 37 protein. We determined the nucleotide sequence of the entire sigma 37 gene, which was found to encode a 262-amino acid residue polypeptide of 29.9 kDa. The predicted amino acid sequence of sigma 37 showed significant homology to that of other sigma proteins in a region that has been proposed to be the site of binding of these factors to core RNA polymerase. Genetic mapping experiments placed the gene for sigma 37, herein designated sigB, at 40 degrees on the genetic map of Piggot and Hoch [Piggot, P. & Hoch, J. A. (1985) Microbiol. Rev. 49, 158-179]. An insertion mutation was constructed in sigB and found not to impair growth or sporulation.
σ37是在革兰氏阳性细菌枯草芽孢杆菌中发现的一种次要的RNA聚合酶σ因子。σ37调控在孢子形成早期开启的基因以及在生长指数期结束时开启但不受孢子形成控制的其他基因的体外转录。为了研究σ37在枯草芽孢杆菌基因表达中的作用,我们通过使用基于σ37蛋白的NH2末端氨基酸序列设计的合成寡核苷酸作为杂交探针,在大肠杆菌中克隆了这种次要σ因子的基因。我们测定了整个σ37基因的核苷酸序列,发现它编码一个29.9 kDa的262个氨基酸残基的多肽。σ37的预测氨基酸序列在一个被认为是这些因子与核心RNA聚合酶结合位点的区域与其他σ蛋白的氨基酸序列具有显著同源性。遗传图谱实验将σ37基因(在此命名为sigB)定位在Piggot和Hoch [Piggot, P. & Hoch, J. A. (1985) Microbiol. Rev. 49, 158 - 179]遗传图谱的40度处。在sigB中构建了一个插入突变,发现它不影响生长或孢子形成。