Department of Molecular and Cellular Biology and Howard Hughes Medical Institute, University of Arizona, Tucson, Arizona 85721-0206, USA.
Cold Spring Harb Perspect Biol. 2012 Sep 1;4(9):a012286. doi: 10.1101/cshperspect.a012286.
The control of translation and mRNA degradation is important in the regulation of eukaryotic gene expression. In general, translation and steps in the major pathway of mRNA decay are in competition with each other. mRNAs that are not engaged in translation can aggregate into cytoplasmic mRNP granules referred to as processing bodies (P-bodies) and stress granules, which are related to mRNP particles that control translation in early development and neurons. Analyses of P-bodies and stress granules suggest a dynamic process, referred to as the mRNA Cycle, wherein mRNPs can move between polysomes, P-bodies and stress granules although the functional roles of mRNP assembly into higher order structures remain poorly understood. In this article, we review what is known about the coupling of translation and mRNA degradation, the properties of P-bodies and stress granules, and how assembly of mRNPs into larger structures might influence cellular function.
翻译和 mRNA 降解的控制在真核基因表达的调控中非常重要。一般来说,翻译和 mRNA 降解主要途径中的步骤相互竞争。未参与翻译的 mRNA 可以聚集形成细胞质 mRNP 颗粒,称为处理体(P 体)和应激颗粒,这些颗粒与控制早期发育和神经元中翻译的 mRNP 颗粒有关。对 P 体和应激颗粒的分析表明,存在一个称为“mRNA 循环”的动态过程,其中 mRNP 可以在多核糖体、P 体和应激颗粒之间移动,尽管 mRNP 组装成更高阶结构的功能作用仍知之甚少。在本文中,我们回顾了已知的翻译和 mRNA 降解的偶联、P 体和应激颗粒的性质,以及 mRNP 组装成更大结构如何影响细胞功能。