HITS-CLIP yields genome-wide insights into brain alternative RNA processing

被引:985
作者
Licatalosi, Donny D. [1 ,2 ]
Mele, Aldo [1 ,2 ]
Fak, John J. [1 ,2 ]
Ule, Jernej [3 ]
Kayikci, Melis [3 ]
Chi, Sung Wook [1 ,2 ]
Clark, Tyson A. [4 ]
Schweitzer, Anthony C. [4 ]
Blume, John E. [4 ]
Wang, Xuning [1 ]
Darnell, Jennifer C. [1 ,2 ]
Darnell, Robert B. [1 ,2 ]
机构
[1] Rockefeller Univ, Mol Neurooncol Lab, New York, NY 10021 USA
[2] Rockefeller Univ, Howard Hughes Med Inst, New York, NY 10021 USA
[3] MRC, Mol Biol Lab, Cambridge CB2 0QH, England
[4] Affymetrix Inc, Express Res, Santa Clara, CA 95051 USA
基金
英国医学研究理事会;
关键词
D O I
10.1038/nature07488
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
Protein - RNA interactions have critical roles in all aspects of gene expression. However, applying biochemical methods to understand such interactions in living tissues has been challenging. Here we develop a genome- wide means of mapping protein - RNA binding sites in vivo, by high- throughput sequencing of RNA isolated by crosslinking immunoprecipitation ( HITS- CLIP). HITS- CLIP analysis of the neuron- specific splicing factor Nova revealed extremely reproducible RNA- binding maps in multiple mouse brains. These maps provide genome- wide in vivo biochemical footprints confirming the previous prediction that the position of Nova binding determines the outcome of alternative splicing; moreover, they are sufficiently powerful to predict Nova action de novo. HITS- CLIP revealed a large number of Nova - RNA interactions in 39 untranslated regions, leading to the discovery that Nova regulates alternative polyadenylation in the brain. HITS- CLIP, therefore, provides a robust, unbiased means to identify functional protein - RNA interactions in vivo.
引用
收藏
页码:464 / U22
页数:7
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