Hu J C, Gross C A
Department of Bacteriology, University of Wisconsin, Madison 53706.
J Mol Biol. 1988 Sep 5;203(1):15-27. doi: 10.1016/0022-2836(88)90087-3.
The sigma subunits of eubacterial RNA polymerases determine the site selectivity of initiation of transcription at promoters. Mutations in rpoD, the gene that encodes sigma 70, the major sigma factor in Escherichia coli, should be useful in determining the molecular details of the process of transcription initiation. However, such mutations are likely to be deleterious or lethal, since sigma70 is an essential gene product. We designed a system for the rapid isolation and fine structure mapping of mutations in rpoD, which allows selection of mutations that would otherwise be deleterious to the cell. We used this system to isolate a new class of mutations in rpoD, mutations that relieve the requirement for CAP-cAMP for initiation at promoters in the mal regulon. These mutations, which we designate rpoD(Mal) mutations, occur in two clusters in the rpoD gene within regions previously suggested by amino acid sequence comparisons to be important for sigma structure or function. We cannot distinguish whether the rpoD(Mal) mutations affect mal expression by altering interaction between RNA polymerase and mal promoters or between RNA polymerase and the accessory transcription factor MalT. However, the effects of the mutations on activator-independent transcription from the lac promoter (4 rpoD(Mal) mutations decrease CAP-independent expression of the lac promoter in vivo) suggest that the regions of sigma identified by our mutations may be directly involved in promoter recognition.
真细菌RNA聚合酶的σ亚基决定了在启动子处转录起始的位点选择性。编码σ⁷⁰(大肠杆菌中的主要σ因子)的基因rpoD发生突变,可能有助于确定转录起始过程的分子细节。然而,此类突变可能具有有害性或致死性,因为σ⁷⁰是一种必需的基因产物。我们设计了一个系统,用于快速分离rpoD中的突变并进行精细结构定位,该系统能够筛选出那些对细胞原本有害的突变。我们利用这个系统在rpoD中分离出了一类新的突变,这类突变能够解除麦芽糖操纵子中启动子起始转录对CAP-cAMP的需求。我们将这些突变命名为rpoD(Mal)突变,它们出现在rpoD基因的两个簇中,位于之前通过氨基酸序列比较推测对σ结构或功能很重要的区域内。我们无法区分rpoD(Mal)突变是通过改变RNA聚合酶与麦芽糖启动子之间的相互作用,还是通过改变RNA聚合酶与辅助转录因子MalT之间的相互作用来影响麦芽糖的表达。然而,这些突变对lac启动子的非激活依赖性转录的影响(4个rpoD(Mal)突变在体内降低了lac启动子的CAP非依赖性表达)表明,我们通过突变确定的σ区域可能直接参与启动子识别。