Structural basis of initial RNA polymerase II transcription

被引:74
作者
Cheung, Alan C. M.
Sainsbury, Sarah
Cramer, Patrick [1 ,2 ]
机构
[1] Univ Munich, Gene Ctr, D-81377 Munich, Germany
[2] Univ Munich, Dept Biochem, CIPSM, D-81377 Munich, Germany
基金
欧洲研究理事会;
关键词
gene transcription; NTP binding; RNA polymerase; transcription initiation; ELONGATION COMPLEX; TRIGGER LOOP; IN-VITRO; DNA; SPECIFICITY;
D O I
10.1038/emboj.2011.396
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During transcription initiation by RNA polymerase (Pol) II, a transient open promoter complex (OC) is converted to an initially transcribing complex (ITC) containing short RNAs, and to a stable elongation complex (EC). We report structures of a Pol II-DNA complex mimicking part of the OC, and of complexes representing minimal ITCs with 2, 4, 5, 6, and 7 nucleotide (nt) RNAs, with and without a non-hydrolyzable nucleoside triphosphate (NTP) in the insertion site +1. The partial OC structure reveals that Pol II positions the melted template strand opposite the active site. The ITC-mimicking structures show that two invariant lysine residues anchor the 3'-proximal phosphate of short RNAs. Short DNA-RNA hybrids adopt a tilted conformation that excludes the +1 template nt from the active site. NTP binding induces complete DNA translocation and the standard hybrid conformation. Conserved NTP contacts indicate a universal mechanism of NTP selection. The essential residue Q1078 in the closed trigger loop binds the NTP 2'-OH group, explaining how the trigger loop couples catalysis to NTP selection, suppressing dNTP binding and DNA synthesis. The EMBO Journal (2011) 30, 4755-4763. doi:10.1038/emboj.2011.396; Published online 4 November 2011
引用
收藏
页码:4755 / 4763
页数:9
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