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真核生物 mRNAs 5'-非翻译区的翻译调控。

Translational control by 5'-untranslated regions of eukaryotic mRNAs.

机构信息

Group on Cell Regulation and Development, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.

Department of Biochemistry and Goodman Cancer Centre, McGill University, Montreal, Quebec H3A 1A3, Canada.

出版信息

Science. 2016 Jun 17;352(6292):1413-6. doi: 10.1126/science.aad9868.

Abstract

The eukaryotic 5' untranslated region (UTR) is critical for ribosome recruitment to the messenger RNA (mRNA) and start codon choice and plays a major role in the control of translation efficiency and shaping the cellular proteome. The ribosomal initiation complex is assembled on the mRNA via a cap-dependent or cap-independent mechanism. We describe various mechanisms controlling ribosome scanning and initiation codon selection by 5' upstream open reading frames, translation initiation factors, and primary and secondary structures of the 5'UTR, including particular sequence motifs. We also discuss translational control via phosphorylation of eukaryotic initiation factor 2, which is implicated in learning and memory, neurodegenerative diseases, and cancer.

摘要

真核生物的 5'非翻译区(UTR)对于核糖体招募到信使 RNA(mRNA)和起始密码子选择至关重要,并且在控制翻译效率和塑造细胞蛋白质组方面发挥着重要作用。核糖体起始复合物通过帽依赖或帽非依赖机制组装在 mRNA 上。我们描述了各种控制核糖体扫描和起始密码子选择的机制,这些机制涉及 5'UTR 的上游开放阅读框、翻译起始因子以及 5'UTR 的一级和二级结构,包括特定的序列基序。我们还讨论了通过真核起始因子 2 的磷酸化进行的翻译控制,该因子与学习和记忆、神经退行性疾病和癌症有关。

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