Wahle E, Rüegsegger U
Institut für Biochemie, Martin-Luther-Universität Halle-Wittenberg, Germany.
FEMS Microbiol Rev. 1999 Jun;23(3):277-95. doi: 10.1111/j.1574-6976.1999.tb00400.x.
3'-Ends of almost all eukaryotic mRNAs are generated by endonucleolytic cleavage and addition of a poly(A) tail. In mammalian cells, the reaction depends on the sequence AAUAAA upstream of the cleavage site, a degenerate GU-rich sequence element downstream of the cleavage site and stimulatory sequences upstream of AAUAAA. Six factors have been identified that carry out the two reactions. With a single exception, they have been purified to homogeneity and cDNAs for 11 subunits have been cloned. Some of the cooperative RNA-protein and protein-protein interactions within the processing complex have been analyzed, but many details, including the identity of the endonuclease, remain unknown. Several examples of regulated polyadenylation are being analyzed at the molecular level. In the yeast Saccharomyces cerevisiae, sequences directing cleavage and polyadenylation are more degenerate than in metazoans, and a downstream element has not been identified. The list of processing factors may be complete now with approximately a dozen polypeptides, but their functions in the reaction are largely unknown. 3'-Processing is known to be coupled to transcription. This connection is thought to involve interactions of processing factors with the mRNA cap as well as with RNA polymerase II.
几乎所有真核生物mRNA的3'末端都是通过核酸内切酶切割并添加聚腺苷酸尾产生的。在哺乳动物细胞中,该反应依赖于切割位点上游的AAUAAA序列、切割位点下游富含GU的简并序列元件以及AAUAAA上游的刺激序列。已鉴定出六种因子来执行这两个反应。除了一个例外,它们都已被纯化至同质,并且已克隆了11个亚基的cDNA。已对加工复合物内的一些RNA-蛋白质和蛋白质-蛋白质协同相互作用进行了分析,但许多细节,包括核酸内切酶的身份,仍然未知。正在分子水平上分析几个受调控的聚腺苷酸化实例。在酿酒酵母中,指导切割和聚腺苷酸化的序列比后生动物中的更简并,并且尚未鉴定出下游元件。加工因子的列表现在可能已完整,大约有十二种多肽,但它们在反应中的功能很大程度上未知。已知3'加工与转录偶联。这种联系被认为涉及加工因子与mRNA帽以及RNA聚合酶II的相互作用。