Promoter-proximal pausing mediated by the exon junction complex regulates splicing

被引:30
作者
Akhtar, Junaid [1 ,5 ]
Kreim, Nastasja [2 ]
Marini, Federico [3 ]
Mohana, Giriram [1 ]
Bruene, Daniel [1 ]
Binder, Harald [4 ]
Roignant, Jean-Yves [1 ]
机构
[1] IMB, Lab RNA Epigenet, D-55128 Mainz, Germany
[2] IMB, Bioinformat Core Facil, D-55128 Mainz, Germany
[3] IMBEI, D-55101 Mainz, Germany
[4] Univ Freiburg, Inst Med Biometry & Stat, Fac Med & Med Ctr, D-79104 Freiburg, Germany
[5] JGU, Inst Neurobiol & Dev Biol, D-55128 Mainz, Germany
关键词
RNA-POLYMERASE-II; PROTEIN-DNA INTERACTIONS; MESSENGER-RNA; TRANSCRIPTION ELONGATION; P-TEFB; CAP-BINDING; HSP70; GENE; CHROMATIN; EIF4AIII; RELEASE;
D O I
10.1038/s41467-019-08381-0
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
Promoter-proximal pausing of RNA polymerase II (Pol II) is a widespread transcriptional regulatory step across metazoans. Here we find that the nuclear exon junction complex (pre-EJC) is a critical and conserved regulator of this process. Depletion of pre-EJC subunits leads to a global decrease in Pol II pausing and to premature entry into elongation. This effect occurs, at least in part, via non-canonical recruitment of pre-EJC components at promoters. Failure to recruit the pre-EJC at promoters results in increased binding of the positive transcription elongation complex (P-TEFb) and in enhanced Pol II release. Notably, restoring pausing is sufficient to rescue exon skipping and the photoreceptor differentiation defect associated with depletion of pre-EJC components in vivo. We propose that the pre-EJC serves as an early transcriptional checkpoint to prevent premature entry into elongation, ensuring proper recruitment of RNA processing components that are necessary for exon definition.
引用
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页数:17
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