Gonzalez Inma, Munita Roberto, Agirre Eneritz, Dittmer Travis A, Gysling Katia, Misteli Tom, Luco Reini F
ATIP-AVENIR team, Institute of Human Genetics, CNRS UPR 1142, Montpellier, France.
Faculty of Biological Sciences, Pontificia Universidad Católica de Chile, Santiago, Chile.
Nat Struct Mol Biol. 2015 May;22(5):370-6. doi: 10.1038/nsmb.3005. Epub 2015 Apr 6.
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.
可变前体mRNA剪接是产生蛋白质多样性所必需的高度细胞类型特异性过程。然而,负责建立和维持可遗传的细胞特异性可变剪接程序的机制仍知之甚少。最近的观察结果表明组蛋白修饰在可变剪接调控中起作用。在这里,我们报告了一种涉及长链非编码RNA(lncRNA)的染色质介导的剪接控制新机制。我们已经鉴定出一种从人FGFR2基因座内产生的进化保守的核反义lncRNA,它促进FGFR2的上皮特异性可变剪接。该lncRNA通过募集多梳蛋白组蛋白和组蛋白去甲基化酶KDM2a来发挥作用,以创建一个染色质环境,该环境会损害对间充质特异性剪接很重要的抑制性染色质剪接衔接复合物的结合。我们的结果揭示了lncRNA通过调节染色质特征在建立和维持细胞特异性可变剪接中的新功能。