Structural basis of reiterative transcription from the pyrG and pyrBI promoters by bacterial RNA polymerase

被引:6
|
作者
Shin, Yeonoh [1 ]
Hedglin, Mark [2 ]
Murakami, Katsuhiko S. [1 ]
机构
[1] Penn State Univ, Dept Biochem & Mol Biol, Ctr RNA Mol Biol, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Chem, 152 Davey Lab, University Pk, PA 16802 USA
基金
美国国家卫生研究院;
关键词
ESCHERICHIA-COLI; X-RAY; OPERON EXPRESSION; BACILLUS-SUBTILIS; CRYSTAL-STRUCTURE; UPP EXPRESSION; SLIPPAGE; INITIATION; COMPLEX; ELONGATION;
D O I
10.1093/nar/gkz1221
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
Reiterative transcription is a non-canonical form of RNA synthesis by RNA polymerase in which a ribonucleotide specified by a single base in the DNA template is repetitively added to the nascent RNA transcript. We previously determined the X-ray crystal structure of the bacterial RNA polymerase engaged in reiterative transcription from the pyrG promoter, which contains eight poly-G RNA bases synthesized using three C bases in the DNA as a template and extends RNA without displacement of the promoter recognition it factor from the core enzyme. In this study, we determined a series of transcript initiation complex structures from the pyrG promoter using soak-trigger-freeze X-ray crystallography. We also performed biochemical assays to monitor template DNA translocation during RNA synthesis from the pyrG promoter and in vitro transcription assays to determine the length of poly-G RNA from the pyrG promoter variants. Our study revealed how RNA slips on template DNA and how RNA polymerase and template DNA determine length of reiterative RNA product. Lastly, we determined a structure of a transcript initiation complex at the pyrBI promoter and proposed an alternative mechanism of RNA slippage and extension requiring the (1- dissociation from the core enzyme.
引用
收藏
页码:2144 / 2155
页数:12
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