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RNA聚合酶II在基因两端暂停并与前体mRNA加工因子结合。

RNA polymerase II pauses and associates with pre-mRNA processing factors at both ends of genes.

作者信息

Glover-Cutter Kira, Kim Soojin, Espinosa Joaquin, Bentley David L

机构信息

Department of Biochemistry and Molecular Genetics, University of Colorado School of Medicine, UCHSC, MS8101, PO Box 6511, Aurora, Colorado 80045, USA.

出版信息

Nat Struct Mol Biol. 2008 Jan;15(1):71-8. doi: 10.1038/nsmb1352. Epub 2007 Dec 23.

Abstract

We investigated co-transcriptional recruitment of pre-mRNA processing factors to human genes. Capping factors associate with paused RNA polymerase II (pol II) at the 5' ends of quiescent genes. They also track throughout actively transcribed genes and accumulate with paused polymerase in the 3' flanking region. The 3' processing factors cleavage stimulation factor and cleavage polyadenylation specificity factor are maximally recruited 0.5-1.5 kilobases downstream of poly(A) sites where they coincide with capping factors, Spt5, and Ser2-hyperphosphorylated, paused pol II. 3' end processing factors also localize at transcription start sites, and this early recruitment is enhanced after polymerase arrest with the elongation factor DRB. These results suggest that promoters may help specify recruitment of 3' end processing factors. We propose a dual-pausing model wherein elongation arrests near the transcription start site and in the 3' flank to allow co-transcriptional processing by factors recruited to the pol II ternary complex.

摘要

我们研究了前体mRNA加工因子与人基因的共转录募集。加帽因子在静止基因的5'端与暂停的RNA聚合酶II(pol II)相关联。它们也贯穿于活跃转录的基因,并与暂停的聚合酶在3'侧翼区域积累。3'加工因子切割刺激因子和切割聚腺苷酸化特异性因子在聚腺苷酸位点下游0.5 - 1.5千碱基处被最大程度地募集,在那里它们与加帽因子、Spt5以及Ser2超磷酸化的暂停pol II重合。3'末端加工因子也定位于转录起始位点,并且在用延伸因子DRB使聚合酶停滞之后,这种早期募集会增强。这些结果表明启动子可能有助于确定3'末端加工因子的募集。我们提出了一种双暂停模型,其中延伸在转录起始位点附近和3'侧翼处停滞,以允许被募集到pol II三元复合物的因子进行共转录加工。

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