INSERM U1212 - CNRS 5320 & Université de Bordeaux, 146 rue Léo Saignat, 33000, Bordeaux, France.
INSERM U1212 - CNRS 5320 & Université de Bordeaux, 146 rue Léo Saignat, 33000, Bordeaux, France.
Biochimie. 2019 Sep;164:105-110. doi: 10.1016/j.biochi.2019.03.016. Epub 2019 Mar 28.
Pre-mRNA 3'-end maturation is achieved by a mechanism requiring four different protein complexes assembled from approximately twenty factors. A global understanding of this essential process is still missing due to the inability to structurally characterize the entire complexes, even though structures of the isolated factors have been obtained. In this review, we summarize recent findings regarding the atomic description of one of the major players, the Cleavage and Polyadenylation Specificity Factor complex (CPSF in human, CPF in yeast). These data provide information on the architecture adopted by the major components of this complex, and on its capacity to recognize the polyadenylation signal sequence.
前体 mRNA 3'-端成熟是通过一种机制实现的,该机制需要大约二十种因子组装而成的四个不同的蛋白质复合物。由于无法对整个复合物进行结构特征描述,即使已经获得了分离因子的结构,对这个基本过程的全面理解仍然缺失。在这篇综述中,我们总结了关于主要参与者之一的切割和多聚腺苷酸化特异性因子复合物(人 CPSF,酵母 CPF)的原子描述的最新发现。这些数据提供了关于该复合物主要成分采用的结构以及其识别多聚腺苷酸化信号序列的能力的信息。