A lncRNA regulates alternative splicing via establishment of a splicing-specific chromatin signature

被引:225
作者
Gonzalez, Inma [1 ]
Munita, Roberto [2 ]
Agirre, Eneritz [1 ]
Dittmer, Travis A. [3 ]
Gysling, Katia [2 ]
Misteli, Tom [3 ]
Luco, Reini F. [1 ]
机构
[1] CNRS, Inst Human Genet, ATIP AVENIR Team, UPR 1142, Montpellier, France
[2] Pontificia Univ Catolica Chile, Fac Biol Sci, Santiago, Chile
[3] NCI, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
LONG NONCODING RNA; HISTONE H3; TRIMETHYLATION; TRANSCRIPTION; EXPRESSION; COMPLEXES;
D O I
10.1038/nsmb.3005
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
Alternative pre-mRNA splicing is a highly cell type-specific process essential to generating protein diversity. However, the mechanisms responsible for the establishment and maintenance of heritable cell-specific alternative-splicing programs are poorly understood. Recent observations point to a role of histone modifications in the regulation of alternative splicing. Here we report a new mechanism of chromatin-mediated splicing control involving a long noncoding RNA (lncRNA). We have identified an evolutionarily conserved nuclear antisense lncRNA, generated from within the human FGFR2 locus, that promotes epithelial-specific alternative splicing of FGFR2. The lncRNA acts through recruitment of Polycomb-group proteins and the histone demethylase KDM2a to create a chromatin environment that impairs binding of a repressive chromatin-splicing adaptor complex important for mesenchymal-specific splicing. Our results uncover a new function for lncRNAs in the establishment and maintenance of cell-specific alternative splicing via modulation of chromatin signatures.
引用
收藏
页码:370 / U111
页数:10
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