Lonetto M A, Rhodius V, Lamberg K, Kiley P, Busby S, Gross C
Department of Stomatology, University of California at San Francisco, San Francisco, CA, 94143, USA.
J Mol Biol. 1998 Dec 18;284(5):1353-65. doi: 10.1006/jmbi.1998.2268.
The sigma subunit of RNA polymerase orchestrates basal transcription by first binding to core RNA polymerase and then recognizing promoters. Using a series of 16 alanine-substitution mutations, we show that residues in a narrow region of Escherichia coli sigma70 (590 to 603) are involved in transcription activation by a mutationally altered CRP derivative, FNR and AraC. Homology modeling of region 4 of sigma70 to the closely related NarL or 434 Cro proteins, suggests that the five basic residues implicated in activation are either in the C terminus of a long recognition helix that includes residues recognizing the -35 hexamer region of the promoter, or in the subsequent loop, and are ideally positioned to permit interaction with activators. The only substitution that has a significant effect on activator-independent transcription is at R603, indicating that this residue of sigma70 may play a distinct role in transcription initiation.
RNA聚合酶的σ亚基首先与核心RNA聚合酶结合,然后识别启动子,从而协调基础转录。通过一系列16个丙氨酸取代突变,我们发现大肠杆菌σ70(590至603)狭窄区域内的残基参与了由突变改变的CRP衍生物、FNR和AraC介导的转录激活。将σ70的区域4与密切相关的NarL或434 Cro蛋白进行同源建模,结果表明,参与激活的五个碱性残基要么位于一个长识别螺旋的C末端,该螺旋包含识别启动子-35六聚体区域的残基,要么位于随后的环中,并且其位置理想,便于与激活剂相互作用。对不依赖激活剂的转录有显著影响的唯一取代发生在R603,这表明σ70的这个残基可能在转录起始中发挥独特作用。