Temme Claudia, Simonelig Martine, Wahle Elmar
Institute of Biochemistry and Biotechnology, Martin Luther University Halle-Wittenberg Halle, Germany.
Genetics and Development, Institute of Human Genetics - CNRS UPR1142 Montpellier, France.
Front Genet. 2014 May 26;5:143. doi: 10.3389/fgene.2014.00143. eCollection 2014.
Controlled shortening of the poly(A) tail of mRNAs is the first step in eukaryotic mRNA decay and can also be used for translational inactivation of mRNAs. The CCR4-NOT complex is the most important among a small number of deadenylases, enzymes catalyzing poly(A) tail shortening. Rates of poly(A) shortening differ between mRNAs as the CCR4-NOT complex is recruited to specific mRNAs by means of either sequence-specific RNA binding proteins or miRNAs. This review summarizes our current knowledge concerning the subunit composition and deadenylation activity of the Drosophila CCR4-NOT complex and the mechanisms by which the complex is recruited to particular mRNAs. We discuss genetic data implicating the complex in the regulation of specific mRNAs, in particular in the context of development.
mRNA 聚腺苷酸尾巴的可控缩短是真核生物 mRNA 降解的第一步,也可用于 mRNA 的翻译失活。CCR4-NOT 复合物是少数几种催化聚腺苷酸尾巴缩短的去腺苷酸化酶中最重要的一种。由于 CCR4-NOT 复合物通过序列特异性 RNA 结合蛋白或 miRNA 被招募到特定的 mRNA 上,所以不同 mRNA 的聚腺苷酸缩短速率有所不同。本综述总结了我们目前关于果蝇 CCR4-NOT 复合物的亚基组成、去腺苷酸化活性以及该复合物被招募到特定 mRNA 的机制的知识。我们讨论了涉及该复合物在特定 mRNA 调控中的遗传数据,特别是在发育背景下。