Intrinsically disordered RGG/RG domains mediate degenerate specificity in RNA binding

被引:160
作者
Ozdilek, Bagdeser A. [1 ]
Thompson, Valery F. [2 ]
Ahmed, Nasiha S. [2 ,3 ]
White, Connor I. [2 ]
Batey, Robert T. [4 ]
Schwartz, Jacob C. [2 ]
机构
[1] Univ Colorado, Dept Mol Cellular & Dev Biol, Campus Box 347, Boulder, CO 80309 USA
[2] Univ Arizona, Dept Chem & Biochem, Tucson, AZ 85721 USA
[3] Univ Arizona, Dept Mol & Cellular Biol, Tucson, AZ 85721 USA
[4] Univ Colorado, Dept Chem & Biochem, Campus Box 596, Boulder, CO 80309 USA
基金
美国国家卫生研究院;
关键词
LOW-COMPLEXITY DOMAINS; CELL-FREE FORMATION; POLYMERASE-II; PROTEIN INTERACTIONS; CRYSTAL-STRUCTURE; PHASE-TRANSITION; MOTIF PROTEINS; MESSENGER-RNAS; LIVING CELLS; FUS PROTEIN;
D O I
10.1093/nar/gkx460
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
RGG/RG domains are the second most common RNA binding domain in the human genome, yet their RNA-binding properties remain poorly understood. Here, we report a detailed analysis of the RNA binding characteristics of intrinsically disordered RGG/RG domains from Fused in Sarcoma (FUS), FMRP and hnRNPU. For FUS, previous studies defined RNA binding as mediated by its well-folded domains; however, we show that RGG/RG domains are the primary mediators of binding. RGG/RG domains coupled to adjacent folded domains can achieve affinities approaching that of full-length FUS. Analysis of RGG/RG domains from FUS, FMRP and hnRNPU against a spectrum of contrasting RNAs reveals that each display degenerate binding specificity, while still displaying different degrees of preference for RNA.
引用
收藏
页码:7984 / 7996
页数:13
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