Alternative Splicing Regulates Biogenesis of miRNAs Located across Exon-Intron Junctions

被引:83
|
作者
Melamed, Ze'ev [1 ]
Levy, Asaf [1 ,3 ]
Ashwal-Fluss, Reut [4 ]
Lev-Maor, Galit [1 ]
Mekahel, Keren [1 ]
Atias, Nir [2 ]
Gilad, Shlomit [3 ]
Sharan, Roded [2 ]
Levy, Carmit [1 ]
Kadener, Sebastian [4 ]
Ast, Gil [1 ]
机构
[1] Tel Aviv Univ, Sackler Fac Med, Dept Human Mol Genet & Biochem, IL-69978 Tel Aviv, Israel
[2] Tel Aviv Univ, Blavatnik Sch Comp Sci, IL-69978 Tel Aviv, Israel
[3] Rosetta Genom Ltd, IL-76706 Rehovot, Israel
[4] Hebrew Univ Jerusalem, Alexander Silberman Inst Life Sci, Dept Biol Chem, IL-91904 Jerusalem, Israel
基金
以色列科学基金会;
关键词
MICRORNA BIOGENESIS; POSTTRANSCRIPTIONAL REGULATION; NUCLEAR EXPORT; PROTEIN; SITES; EXPRESSION; APOPTOSIS; DROSHA; GENES; MOUSE;
D O I
10.1016/j.molcel.2013.05.007
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
The initial step in microRNA (miRNA) biogenesis requires processing of the precursor miRNA (pre-miRNA) from a longer primary transcript. Many pre-miRNAs originate from introns, and both a mature miRNA and a spliced RNA can be generated from the same transcription unit. We have identified a mechanism in which RNA splicing negatively regulates the processing of pre-miRNAs that overlap exon-intron junctions. Computational analysis identified dozens of such pre-miRNAs, and experimental validation demonstrated competitive interaction between the Microprocessor complex and the splicing machinery. Tissue-specific alternative splicing regulates maturation of one such miRNA, miR-412, resulting in effects on its targets that code a protein network involved in neuronal cell death processes. This mode of regulation specifically controls maturation of splice-site-overlapping pre-miRNAs but not pre-miRNAs located completely within introns or exons of the same transcript. Our data present a biological role of alternative splicing in regulation of miRNA biogenesis.
引用
收藏
页码:869 / 881
页数:13
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