Parker Roy, Song Haiwei
Department of Molecular and Cellular Biology and Howard Hughes Medical Institute, University of Arizona, 1007 E. Lowell Street, Tucson, Arizona 85721-0106, USA.
Nat Struct Mol Biol. 2004 Feb;11(2):121-7. doi: 10.1038/nsmb724.
The degradation of eukaryotic mRNAs plays important roles in the modulation of gene expression, quality control of mRNA biogenesis and antiviral defenses. In the past five years, many of the enzymes involved in this process have been identified and mechanisms that modulate their activities have begun to be identified. In this review, we describe the enzymes of mRNA degradation and their properties. We highlight that there are a variety of enzymes with different specificities, suggesting that individual nucleases act on distinct subpopulations of transcripts within the cell. In several cases, translation factors that bind mRNA inhibit these nucleases. In addition, recent work has begun to identify distinct mRNP complexes that recruit the nucleases to transcripts through different mRNA-interacting proteins. These properties and complexes suggest multiple mechanisms by which mRNA degradation could be regulated.
真核生物信使核糖核酸(mRNA)的降解在基因表达调控、mRNA生物合成的质量控制以及抗病毒防御中发挥着重要作用。在过去五年中,参与这一过程的许多酶已被鉴定出来,并且调节其活性的机制也已开始被明确。在本综述中,我们描述了mRNA降解的酶及其特性。我们强调存在多种具有不同特异性的酶,这表明单个核酸酶作用于细胞内不同的转录本子群体。在几种情况下,结合mRNA的翻译因子会抑制这些核酸酶。此外,最近的研究已开始鉴定不同的信使核糖核蛋白(mRNP)复合物,这些复合物通过不同的mRNA相互作用蛋白将核酸酶招募到转录本上。这些特性和复合物提示了mRNA降解可能被调控的多种机制。