Kulbachinskiy Andrey, Mustaev Arkady
Institute of Molecular Genetics, Russian Academy of Sciences, Moscow 123182, Russia.
J Biol Chem. 2006 Jul 7;281(27):18273-6. doi: 10.1074/jbc.C600060200. Epub 2006 May 10.
Region 3.2 of the RNA polymerase sigma subunit forms a loop that protrudes toward RNA polymerase active center and partially blocks RNA exit channel. To provide some insights into the functional role of this region, we studied a deletion variant of the Escherichia coli sigma(70) subunit that lacked amino acids 513-519 corresponding to the tip of the loop. The deletion had multiple effects on transcription initiation including: (i) a significant decrease in the amount of short abortive RNAs synthesized during initiation, (ii) defects in promoter escape, (iii) loss of the contacts between the sigma subunit and the nascent RNA during initiation and, finally, (iv) dramatic increase in the K(m) value for the 3'-initiating nucleotide. At the same time, the mutation did not impair promoter opening and the binding of the 5'-initiating purine nucleotide. In summary, our data demonstrate an important role of sigma region 3.2 in the binding of initiating substrates in RNA polymerase active center and in the process of promoter clearance.
RNA聚合酶σ亚基的3.2区域形成一个环,该环向RNA聚合酶活性中心突出并部分阻塞RNA出口通道。为了深入了解该区域的功能作用,我们研究了大肠杆菌σ⁷⁰亚基的一个缺失变体,该变体缺少对应于环尖端的氨基酸513 - 519。该缺失对转录起始有多种影响,包括:(i)起始过程中合成的短流产RNA数量显著减少,(ii)启动子逃逸缺陷,(iii)起始过程中σ亚基与新生RNA之间的接触丧失,最后,(iv)3'-起始核苷酸的Kₘ值急剧增加。同时,该突变不影响启动子开放和5'-起始嘌呤核苷酸的结合。总之,我们的数据证明了σ亚基3.2区域在RNA聚合酶活性中心起始底物结合和启动子清除过程中的重要作用。