RNA targets of wild-type and mutant FET family proteins

被引:273
作者
Hoell, Jessica I. [1 ,2 ]
Larsson, Erik [3 ]
Runge, Simon [1 ]
Nusbaum, Jeffrey D. [1 ]
Duggimpudi, Sujitha [2 ]
Farazi, Thalia A. [1 ]
Hafner, Markus [1 ]
Borkhardt, Arndt [2 ]
Sander, Chris [3 ]
Tuschl, Thomas [1 ]
机构
[1] Rockefeller Univ, Howard Hughes Med Inst, Lab RNA Mol Biol, New York, NY 10021 USA
[2] Univ Dusseldorf, Ctr Child & Adolescent Hlth, Dept Pediat Oncol Hematol & Clin Immunol, D-40225 Dusseldorf, Germany
[3] Mem Sloan Kettering Canc Ctr, Computat Biol Ctr, New York, NY 10021 USA
基金
美国国家卫生研究院; 瑞典研究理事会;
关键词
AMYOTROPHIC-LATERAL-SCLEROSIS; GENE; IDENTIFICATION; TRANSLATION; MUTATIONS; DISEASE; SITES; CLIP;
D O I
10.1038/nsmb.2163
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
FUS, EWSR1 and TAF15, constituting the FET protein family, are abundant, highly conserved RNA-binding proteins with important roles in oncogenesis and neuronal disease, yet their RNA targets and recognition elements are unknown. Using PAR-CLIP, we defined global RNA targets for all human FET proteins and two ALS-causing human FUS mutants. FET members showed similar binding profiles, whereas FUS mutants showed a drastically altered binding pattern, consistent with changes in subcellular localization.
引用
收藏
页码:1428 / 1431
页数:4
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