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Formation of mRNA 3′ Ends in Eukaryotes: Mechanism Regulation and Interrelationships with Other Steps in mRNA Synthesis

机译:真核生物中的mRNA 3末端的形成:机制调控和与mRNA合成其他步骤的相互关系。

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摘要

Formation of mRNA 3′ ends in eukaryotes requires the interaction of transacting factors with cis-acting signal elements on the RNA precursor by two distinct mechanisms, one for the cleavage of most replication-dependent histone transcripts and the other for cleavage and polyadenylation of the majority of eukaryotic mRNAs. Most of the basic factors have now been identified, as well as some of the key protein-protein and RNA-protein interactions. This processing can be regulated by changing the levels or activity of basic factors or by using activators and repressors, many of which are components of the splicing machinery. These regulatory mechanisms act during differentiation, progression through the cell cycle, or viral infections. Recent findings suggest that the association of cleavage/polyadenylation factors with the transcriptional complex via the carboxyl-terminal domain of the RNA polymerase II (Pol II) large subunit is the means by which the cell restricts polyadenylation to Pol II transcripts. The processing of 3′ ends is also important for transcription termination downstream of cleavage sites and for assembly of an export-competent mRNA. The progress of the last few years points to a remarkable coordination and cooperativity in the steps leading to the appearance of translatable mRNA in the cytoplasm.
机译:真核生物中mRNA 3'末端的形成需要通过两种不同的机制使交易因子与RNA前体上的顺式作用信号元件相互作用,一种机制是裂解大多数复制依赖性组蛋白转录本,另一种机制是裂解大多数复制依赖性组蛋白转录本。真核mRNA。现在已经确定了大多数基本因素,以及一些关键的蛋白质-蛋白质和RNA-蛋白质相互作用。可以通过更改基本因子的水平或活性或使用激活剂和阻遏剂来调节此过程,其中许多激活剂和阻遏剂是拼接机械的组成部分。这些调节机制在分化,整个细胞周期进展或病毒感染期间起作用。最近的发现表明,通过RNA聚合酶II(Pol II)大亚基的羧基末端结构域,裂解/聚腺苷酸化因子与转录复合物的缔合是细胞将聚腺苷酸化限制于Pol II转录物的手段。 3'端的加工对于裂解位点下游的转录终止和出口能力mRNA的组装也很重要。最近几年的进展表明,在导致可翻译的mRNA在细胞质中出现的步骤中,它们具有显着的协调性和协同性。

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