Defining the RGG/RG Motif

被引:491
作者
Thandapani, Palaniraja [1 ,2 ,3 ,4 ]
O'Connor, Timothy R. [5 ]
Bailey, Timothy L. [5 ]
Richard, Stephane [1 ,2 ,3 ,4 ]
机构
[1] McGill Univ, Terry Fox Mol Oncol Grp, Montreal, PQ H3T 1E2, Canada
[2] McGill Univ, Bloomfield Ctr Res Aging, Lady Davis Inst Med Res, Montreal, PQ H3T 1E2, Canada
[3] McGill Univ, Dept Oncol, Montreal, PQ H3T 1E2, Canada
[4] McGill Univ, Dept Med, Montreal, PQ H3T 1E2, Canada
[5] Univ Queensland, Inst Mol Biosci, Brisbane, Qld 4072, Australia
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
MENTAL-RETARDATION PROTEIN; CYTOPLASMIC STRESS GRANULES; EWINGS-SARCOMA PROTEIN; RNA-BINDING PROTEIN; SMN TUDOR DOMAIN; FRAGILE-X; ARGININE METHYLATION; MESSENGER-RNA; STRUCTURAL BASIS; DEPENDENT RECOGNITION;
D O I
10.1016/j.molcel.2013.05.021
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
Motifs rich in arginines and glycines were recognized several decades ago to play functional roles and were termed glycine-arginine-rich (GAR) domains and/or RGG boxes. We review here the evolving functions of the RGG box along with several sequence variations that we collectively term the RGG/RG motif. Greater than 1,000 human proteins harbor the RGG/RG motif, and these proteins influence numerous physiological processes such as transcription, pre-mRNA splicing, DNA damage signaling, mRNA translation, and the regulation of apoptosis. In particular, we discuss the role of the RGG/RG motif in mediating nucleic acid and protein interactions, a function that is often regulated by arginine methylation and partner-binding proteins. The physiological relevance of the RGG/RG motif is highlighted by its association with several diseases including neurological and neuromuscular diseases and cancer. Herein, we discuss the evidence for the emerging diverse functionality of this important motif.
引用
收藏
页码:613 / 623
页数:11
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