Architecture of RNA polymerase II and implications for the transcription mechanism

被引:462
|
作者
Cramer, P
Bushnell, DA
Fu, JH
Gnatt, AL
Maier-Davis, B
Thompson, NE
Burgess, RR
Edwards, AM
David, PR
Kornberg, RD [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Biol Struct, Stanford, CA 94305 USA
[2] Univ Wisconsin, Mcardle Lab Canc Res, Madison, WI 53706 USA
[3] Univ Toronto, Banting & Best Dept Med Res, Toronto, ON M5G 1L6, Canada
关键词
D O I
10.1126/science.288.5466.640
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A backbone model of a 10-subunit yeast RNA polymerase II has been derived from x-ray diffraction data extending to 3 angstroms resolution. All 10 subunits exhibit a high degree of identity with the corresponding human proteins, and 9 of the 10 subunits are conserved among the three eukaryotic RNA polymerases I, II, and III. Notable features of the model include a pair of jaws, formed by subunits Rpb1, Rpb5, and Rpb9, that appear to grip DNA downstream of the active center. A clamp on the DNA nearer the active center, formed by Rpb1, Rpb2, and Rpb6, may be Locked in the closed position by RNA, accounting for the great stability of transcribing complexes. A pore in the protein complex beneath the active center may allow entry of substrates for polymerization and exit of the transcript during proofreading and passage through pause sites in the DNA.
引用
收藏
页码:640 / 649
页数:10
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