Global Analysis of Nascent RNA Reveals Transcriptional Pausing in Terminal Exons

被引:184
作者
Oesterreich, Fernando Carrillo [1 ]
Preibisch, Stephan [1 ]
Neugebauer, Karla M. [1 ]
机构
[1] Max Planck Inst Mol Biol & Genet, D-01307 Dresden, Germany
关键词
POLYMERASE-II TRANSCRIPTION; IN-VIVO; YEAST GENOME; HUMAN GENES; POL-II; SPLICEOSOME; ELONGATION; DYNAMICS; CELLS; RECRUITMENT;
D O I
10.1016/j.molcel.2010.11.004
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
Pre-mRNA splicing is catalyzed by the spliceosome, which can assemble on pre-mRNA cotranscriptionally. However, whether splicing generally occurs during transcription has not been addressed. Indeed, splicing catalysis is expected to occur posttranscriptionally in yeast, where the shortness of terminal exons should leave insufficient time for splicing. Here, we isolate endogenous S. cerevisiae nascent RNA and determine gene-specific splicing efficiencies and transcription profiles, using high-density tiling microarrays. Surprisingly, we find that splicing occurs cotranscriptionally for the majority of intron-containing genes. Analysis of transcription profiles reveals Pot II pausing within the terminal exons of these genes. Intronless and inefficiently spliced genes lack this pause. In silico simulations of transcription and splicing kinetics confirm that this pausing event provides sufficient time for splicing before termination. The discovery of terminal exon pausing demonstrates functional coupling of transcription and splicing near gene ends.
引用
收藏
页码:571 / 581
页数:11
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