Histone Deacetylase Activity Modulates Alternative Splicing

被引:112
作者
Hnilicova, Jarmila [1 ]
Hozeifi, Samira [1 ]
Duskova, Eva [1 ]
Icha, Jaroslav [1 ]
Tomankova, Tereza [1 ]
Stanek, David [1 ]
机构
[1] Inst Mol Genet AS CR, Dept RNA Biol, Prague, Czech Republic
来源
PLOS ONE | 2011年 / 6卷 / 02期
关键词
PRE-MESSENGER-RNA; FIBRONECTIN EIIIB EXON; II TRANSCRIPTION; SR PROTEINS; IN-VIVO; CHROMATIN; ELONGATION; POLYMERASE; ACETYLATION; RECRUITMENT;
D O I
10.1371/journal.pone.0016727
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
There is increasing evidence to suggest that splicing decisions are largely made when the nascent RNA is still associated with chromatin. Here we demonstrate that activity of histone deacetylases (HDACs) influences splice site selection. Using splicing-sensitive microarrays, we identified similar to 700 genes whose splicing was altered after HDAC inhibition. We provided evidence that HDAC inhibition induced histone H4 acetylation and increased RNA Polymerase II (Pol II) processivity along an alternatively spliced element. In addition, HDAC inhibition reduced co-transcriptional association of the splicing regulator SRp40 with the target fibronectin exon. We further showed that the depletion of HDAC1 had similar effect on fibronectin alternative splicing as global HDAC inhibition. Importantly, this effect was reversed upon expression of mouse HDAC1 but not a catalytically inactive mutant. These results provide a molecular insight into a complex modulation of splicing by HDACs and chromatin modifications.
引用
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页数:11
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