Mechanism of Eukaryotic RNA Polymerase III Transcription Termination

被引:108
|
作者
Nielsen, Soren [1 ]
Yuzenkova, Yulia [1 ]
Zenkin, Nikolay [1 ]
机构
[1] Newcastle Univ, Ctr Bacterial Cell Biol, Inst Cell & Mol Biosci, Newcastle Upon Tyne NE2 4AX, Tyne & Wear, England
基金
英国生物技术与生命科学研究理事会; 欧洲研究理事会;
关键词
STRUCTURAL BASIS; ACTIVE-CENTER; DNA HYBRID; ELONGATION;
D O I
10.1126/science.1237934
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
Gene expression in organisms involves many factors and is tightly controlled. Although much is known about the initial phase of transcription by RNA polymerase III (Pol III), the enzyme that synthesizes the majority of RNA molecules in eukaryotic cells, termination is poorly understood. Here, we show that the extensive structure of Pol III-synthesized transcripts dictates the release of elongation complexes at the end of genes. The poly-T termination signal, which does not cause termination in itself, causes catalytic inactivation and backtracking of Pol III, thus committing the enzyme to termination and transporting it to the nearest RNA secondary structure, which facilitates Pol III release. Similarity between termination mechanisms of Pol III and bacterial RNA polymerase suggests that hairpin-dependent termination may date back to the common ancestor of multisubunit RNA polymerases.
引用
收藏
页码:1577 / 1580
页数:4
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