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Merck
CN

Cap-binding protein 4EHP effects translation silencing by microRNAs.

Proceedings of the National Academy of Sciences of the United States of America (2017-05-11)
Clément Chapat, Seyed Mehdi Jafarnejad, Edna Matta-Camacho, Geoffrey G Hesketh, Idit A Gelbart, Jan Attig, Christos G Gkogkas, Tommy Alain, Noam Stern-Ginossar, Marc R Fabian, Anne-Claude Gingras, Thomas F Duchaine, Nahum Sonenberg
摘要

MicroRNAs (miRNAs) play critical roles in a broad variety of biological processes by inhibiting translation initiation and by destabilizing target mRNAs. The CCR4-NOT complex effects miRNA-mediated silencing, at least in part through interactions with 4E-T (eIF4E transporter) protein, but the precise mechanism is unknown. Here we show that the cap-binding eIF4E-homologous protein 4EHP is an integral component of the miRNA-mediated silencing machinery. We demonstrate that the cap-binding activity of 4EHP contributes to the translational silencing by miRNAs through the CCR4-NOT complex. Our results show that 4EHP competes with eIF4E for binding to 4E-T, and this interaction increases the affinity of 4EHP for the cap. We propose a model wherein the 4E-T/4EHP interaction engenders a closed-loop mRNA conformation that blocks translational initiation of miRNA targets.

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单克隆抗-FLAG® M2 小鼠抗, clone M2, purified immunoglobulin (Purified IgG1 subclass), buffered aqueous solution (10 mM sodium phosphate, 150 mM NaCl, pH 7.4, containing 0.02% sodium azide)
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单克隆抗 β-肌动蛋白抗体 小鼠抗, clone AC-15, ascites fluid
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抗-HA 兔抗, affinity isolated antibody, buffered aqueous solution