从范式转变的见解:聚(a)结合蛋白如何带来翻译mrna的完整循环

D. Gallie
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引用次数: 4

摘要

近年来,我们对蛋白质合成起始过程的认识发生了巨大的变化。起始被认为只涉及发生在5 '帽结构或其附近的事件,该结构作为帽结合复合物的结合位点,帽结合复合物是一组翻译起始因子(eif),促进40s核糖体亚基与mRNA的结合。由于聚(A)结合蛋白(PABP)与mRNA 3 '端存在的聚(A)尾部结合,因此长期以来被认为在翻译起始中没有作用。在这篇综述中,我提出了来自我的实验室的证据,这些证据有助于我们在翻译过程中如何看待mrna的范式转变。将mRNA描述为直分子,其中poly(A)尾巴远离5 '端发生的事件,现在已经被环状mRNA的概念所取代,其中PABP和帽结合复合物之间的相互作用连接mRNA的末端并促进翻译起始。我实验室的研究支持大多数mRNA的翻译需要mRNA末端之间的功能和物理相互作用的新范式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Insights from a Paradigm Shift: How the Poly(A)-Binding Protein Brings Translating mRNAs Full Circle
In recent years, our thinking of how the initiation of protein synthesis occurs has changed dramatically. Initiation was thought to involve only events occurring at or near the 5′-cap structure, which serves as the binding site for the cap-binding complex, a group of translation initiation factors (eIFs) that facilitate the binding of the 40 S ribosomal subunit to an mRNA. Because the poly(A)-binding protein (PABP) binds the poly(A) tail present at the 3′-terminus of an mRNA, it was long thought to play no role in translation initiation. In this review, I present evidence from my laboratory that has contributed to the paradigm shift in how we think of mRNAs during translation. The depiction of mRNAs as straight molecules in which the poly(A) tail is far from events occurring at the 5′-end has now been replaced by the concept of a circular mRNA where the interaction between PABP and the cap-binding complex bridges the termini of an mRNA and promotes translation initiation. The research from my laboratory supports the new paradigm that translation of most mRNAs requires a functional and physical interaction between the termini of an mRNA.
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