共 33 条
Ago2/miRISC-mediated inhibition of CBP80/20-dependent translation and thereby abrogation of nonsense-mediated mRNA decay require the cap-associating activity of Ago2
被引:17
作者:
Choe, Junho
[1
]
Cho, Hana
[1
]
Chi, Sung-Gil
[1
]
Kim, Yoon Ki
[1
]
机构:
[1] Korea Univ, Sch Life Sci & Biotechnol, Seoul 136701, South Korea
关键词:
Ago2;
MicroRNA;
NMD;
CBP80/20;
eIF4E;
PROCESSING BODIES;
COMPLEX;
GW182;
DEGRADATION;
ARGONAUTE;
DOMAIN;
SURVEILLANCE;
REPRESSION;
MIRNAS;
D O I:
10.1016/j.febslet.2011.07.047
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:
Nuclear cap-binding protein (CBP) 80/20-dependent translation (CT) is one of the targets for miRNA-mediated gene silencing. Here, we provide evidence that human argonaute 2 (Ago2) competes with CBP80/20 for cap-association, inhibiting CT and thus nonsense-mediated mRNA decay (NMD), which is tightly coupled to CT. Tethering of Ago2, but not of Ago2F2V2 which lacks cap -association activity, to the 3'UTR of PTC-containing mRNA abrogates NMD. Immunoprecipitation using CBP80 antibody reveals that Ago2, but not Ago2F2V2, inhibits the binding of CBP80/20 to cap structure. Our observations provide molecular insight into the cross-talk between miRNA-mediated gene silencing, CT, and NMD. Structured summary of protein interactions: AGO2 physically interacts with GW182 by anti tag coimmunoprecipitation (View interaction) (C) 2011 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2682 / 2687
页数:6
相关论文