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真核翻译起始中 mRNA 扫描时起始密码子的选择。

Selection of start codon during mRNA scanning in eukaryotic translation initiation.

机构信息

Center for Condensed Matter Theory, Department of Physics, Indian Institute of Science, Bangalore, 560012, India.

Department of Chemical Engineering, University of New Hampshire, Durham, NH-03824, USA.

出版信息

Commun Biol. 2022 Jun 15;5(1):587. doi: 10.1038/s42003-022-03534-2.

Abstract

Accurate and high-speed scanning and subsequent selection of the correct start codon are important events in protein synthesis. Eukaryotic mRNAs have long 5' UTRs that are inspected for the presence of a start codon by the ribosomal 48S pre-initiation complex (PIC). However, the conformational state of the 48S PIC required for inspecting every codon is not clearly understood. Here, atomistic molecular dynamics (MD) simulations and energy calculations suggest that the scanning conformation of 48S PIC may reject all but 4 (GUG, CUG, UUG and ACG) of the 63 non-AUG codons, and initiation factor eIF1 is crucial for this discrimination. We provide insights into the possible role of initiation factors eIF1, eIF1A, eIF2α and eIF2β in scanning. Overall, the study highlights how the scanning conformation of ribosomal 48S PIC acts as a coarse selectivity checkpoint for start codon selection and scans long 5' UTRs in eukaryotic mRNAs with accuracy and high speed.

摘要

准确而高速的扫描以及随后正确起始密码子的选择是蛋白质合成中的重要事件。真核生物的 mRNA 具有长的 5'UTR,核糖体 48S 起始前复合物(PIC)通过这些 5'UTR 来检测起始密码子的存在。然而,用于检查每个密码子的 48S PIC 的构象状态尚不清楚。本文通过原子分子动力学(MD)模拟和能量计算表明,48S PIC 的扫描构象可能会拒绝除 63 个非 AUG 密码子中的 4 个(GUG、CUG、UUG 和 ACG),起始因子 eIF1 对于这种区分至关重要。我们深入了解了起始因子 eIF1、eIF1A、eIF2α 和 eIF2β 在扫描过程中的可能作用。总的来说,该研究强调了核糖体 48S PIC 的扫描构象如何作为起始密码子选择的粗选性检查点,以高精度和高速扫描真核生物 mRNA 中的长 5'UTR。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/887b/9200866/50f57bd48388/42003_2022_3534_Fig1_HTML.jpg

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