Orientation of the central domains of KSRP and its implications for the interaction with the RNA targets

被引:41
作者
Diaz-Moreno, Irene [1 ,2 ]
Hollingworth, David [1 ]
Kelly, Geoff
Martin, Stephen [3 ]
Garcia-Mayoral, MariaFlor [1 ]
Briata, Paola [4 ]
Gherzi, Roberto [4 ]
Ramos, Andres [1 ]
机构
[1] Natl Inst Med Res, MRC, Mol Struct Div, London NW7 1AA, England
[2] US CSIC, Inst Bioquim Vegetal & Fotosintesis, Seville 41092, Spain
[3] Natl Inst Med Res, MRC, Div Phys Biochem, London NW7 1AA, England
[4] Ist Nazl Ric Canc, I-16132 Genoa, Italy
基金
英国惠康基金;
关键词
AU-RICH ELEMENTS; NMR-SPECTROSCOPY; KH DOMAINS; BACKBONE DYNAMICS; BINDING-PROTEINS; SEQUENCE; DEGRADATION; RECOGNITION; RELAXATION; CALMODULIN;
D O I
10.1093/nar/gkq216
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
KSRP is a multi-domain RNA-binding protein that recruits the exosome-containing mRNA degradation complex to mRNAs coding for cellular proliferation and inflammatory response factors. The selectivity of this mRNA degradation mechanism relies on KSRP recognition of AU-rich elements in the mRNA 3'UTR, that is mediated by KSRP's KH domains. Our structural analysis shows that the inter-domain linker orients the two central KH domains of KSRP-and their RNA-binding surfaces-creating a two-domain unit. We also show that this inter-domain arrangement is important to the interaction with KSRP's RNA targets.
引用
收藏
页码:5193 / 5205
页数:13
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