Kornblihtt Alberto R, de la Mata Manuel, Fededa Juan Pablo, Munoz Manuel J, Nogues Guadalupe
Departamento de Fisiología, Biología Molecular y Celular, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, IFIByNE-CONICET, Ciudad Universitaria, Pabellón II (C1428EHA) Buenos Aires, Argentina.
RNA. 2004 Oct;10(10):1489-98. doi: 10.1261/rna.7100104.
Transcription and pre-mRNA splicing are extremely complex multimolecular processes that involve protein-DNA, protein-RNA, and protein-protein interactions. Splicing occurs in the close vicinity of genes and is frequently cotranscriptional. This is consistent with evidence that both processes are coordinated and, in some cases, functionally coupled. This review focuses on the roles of cis- and trans-acting factors that regulate transcription, on constitutive and alternative splicing. We also discuss possible functions in splicing of the C-terminal domain (CTD) of the RNA polymerase II (pol II) largest subunit, whose participation in other key pre-mRNA processing reactions (capping and cleavage/polyadenylation) is well documented. Recent evidence indicates that transcriptional elongation and splicing can be influenced reciprocally: Elongation rates control alternative splicing and splicing factors can, in turn, modulate pol II elongation. The presence of transcription factors in the spliceosome and the existence of proteins, such as the coactivator PGC-1, with dual activities in splicing and transcription can explain the links between both processes and add a new level of complexity to the regulation of gene expression in eukaryotes.
转录和前体mRNA剪接是极其复杂的多分子过程,涉及蛋白质-DNA、蛋白质-RNA和蛋白质-蛋白质相互作用。剪接发生在基因附近,且通常是共转录的。这与两个过程相互协调且在某些情况下功能偶联的证据一致。本综述重点关注调控转录的顺式和反式作用因子的作用,以及组成型剪接和可变剪接。我们还讨论了RNA聚合酶II(pol II)最大亚基的C末端结构域(CTD)在剪接中的可能功能,其参与其他关键的前体mRNA加工反应(加帽和切割/聚腺苷酸化)已有充分记录。最近的证据表明转录延伸和剪接可以相互影响:延伸速率控制可变剪接,而剪接因子反过来可以调节pol II延伸。剪接体中转录因子的存在以及诸如共激活因子PGC-1等在剪接和转录中具有双重活性的蛋白质的存在,可以解释这两个过程之间的联系,并为真核生物基因表达调控增加新的复杂程度。