Severinov K, Mustaev A, Kukarin A, Muzzin O, Bass I, Darst S A, Goldfarb A
The Rockefeller University, New York, New York 10021, USA.
J Biol Chem. 1996 Nov 1;271(44):27969-74. doi: 10.1074/jbc.271.44.27969.
The beta and beta' subunits of Escherichia coli DNA-dependent RNA polymerase are highly conserved throughout eubacterial and eukaryotic kingdoms. However, in some archaebacteria and chloroplasts, the corresponding sequences are "split" into smaller polypeptides that are encoded by separate genes. To test if such split sites can be accommodated into E. coli RNA polymerase, subunit fragments encoded by the segments of E. coli rpoB and rpoC genes corresponding to archaebacterial and chloroplast split subunits were individually overexpressed. The purified fragments, when mixed in vitro with complementing intact RNA polymerase subunits, yielded an active enzyme capable of catalyzing the phosphodiester bond formation. Thus, the large subunits of eubacteria and eukaryotes are composed of independent structural modules corresponding to the smaller subunits of archaebacteria and chloroplasts.
大肠杆菌DNA依赖性RNA聚合酶的β亚基和β'亚基在整个真细菌和真核生物界中高度保守。然而,在一些古细菌和叶绿体中,相应的序列被“分割”成由不同基因编码的较小多肽。为了测试这种分割位点是否能被整合到大肠杆菌RNA聚合酶中,分别过量表达了由大肠杆菌rpoB和rpoC基因中与古细菌和叶绿体分割亚基相对应的片段所编码的亚基片段。当在体外将纯化的片段与互补的完整RNA聚合酶亚基混合时,产生了一种能够催化磷酸二酯键形成的活性酶。因此,真细菌和真核生物的大亚基由与古细菌和叶绿体的较小亚基相对应的独立结构模块组成。