共 148 条
Biochemical Properties and Biological Functions of FET Proteins
被引:146
作者:

Schwartz, Jacob C.
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机构:
Univ Colorado, Dept Chem & Biochem, Howard Hughes Med Inst, Boulder, CO 80309 USA Univ Colorado, Dept Chem & Biochem, Howard Hughes Med Inst, Boulder, CO 80309 USA

Cech, Thomas R.
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h-index: 0
机构: Univ Colorado, Dept Chem & Biochem, Howard Hughes Med Inst, Boulder, CO 80309 USA

Parker, Roy R.
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h-index: 0
机构: Univ Colorado, Dept Chem & Biochem, Howard Hughes Med Inst, Boulder, CO 80309 USA
机构:
[1] Univ Colorado, Dept Chem & Biochem, Howard Hughes Med Inst, Boulder, CO 80309 USA
来源:
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 84
|
2015年
/
84卷
关键词:
FUS;
EWSR1;
TAF15;
low-complexity;
RNA-binding;
neurodegeneration;
RNA-BINDING PROTEIN;
AMYOTROPHIC-LATERAL-SCLEROSIS;
NUCLEAR RIBONUCLEOPROTEIN-K;
PRO-ONCOPROTEIN TLS/FUS;
EWINGS-SARCOMA PROTEIN;
HUMAN MYELOID-LEUKEMIA;
NEURON DISEASES ALS;
CELL-FREE FORMATION;
FUSION PROTEIN;
POLYMERASE-II;
D O I:
10.1146/annurev-biochem-060614-034325
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:
Members of the FET protein family, consisting of FUS, EWSR1, and TAF15, bind to RNA and contribute to the control of transcription, RNA processing, and the cytoplasmic fates of messenger RNAs in metazoa. FET proteins can also bind DNA, which may be important in transcription and DNA damage responses. FET proteins are of medical interest because chromosomal rearrangements of their genes promote various sarcomas and because point mutations in FUS or TAF15 can cause neurodegenerative diseases such as amyotrophic lateral sclerosis and frontotemporal lobar dementia. Recent results suggest that both the normal and pathological effects of FET proteins are modulated by low-complexity or prion-like domains, which can form higher-order assemblies with novel interaction properties. Herein, we review FET proteins with an emphasis on how the biochemical properties of FET proteins may relate to their biological functions and to pathogenesis.
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页码:355 / 379
页数:25
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