Misra Ashish, Green Michael R
a Howard Hughes Medical Institute and Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School , Worcester , MA USA.
RNA Biol. 2016;13(3):259-64. doi: 10.1080/15476286.2015.1112490. Epub 2015 Nov 17.
Recent genome-wide protein-RNA interaction studies have significantly reshaped our understanding of the role of mRNA 3' end formation factors in RNA biology. Originally thought to function solely in mediating cleavage and polyadenylation of mRNAs during their maturation, 3' end formation factors have now been shown to play a role in alternative splicing, even at internal introns--an unanticipated role for factors thought only to act at the 3' end of the mRNA. Here, we discuss the recent advances in our understanding of the role of 3' end formation factors in promoting global changes in alternative splicing at internal exon-intron junctions and how they act as cofactors for well known splicing regulators. Additionally, we review the mechanism by which these factors affect the recruitment of early intron recognition components to the 5' and 3' splice site. Our understanding of the roles of 3' end formation factors is still evolving, and the final picture might be more complex than originally envisioned.
最近的全基因组蛋白质-RNA相互作用研究显著重塑了我们对mRNA 3'末端形成因子在RNA生物学中作用的理解。3'末端形成因子最初被认为仅在mRNA成熟过程中介导其切割和多聚腺苷酸化,现在已被证明在可变剪接中发挥作用,甚至在内含子内部——这是一个仅被认为作用于mRNA 3'末端的因子所具有的意外作用。在这里,我们讨论了在理解3'末端形成因子在促进内含子-外显子连接处可变剪接的全局变化中的作用方面的最新进展,以及它们如何作为著名剪接调节因子的辅助因子发挥作用。此外,我们回顾了这些因子影响早期内含子识别成分募集到5'和3'剪接位点的机制。我们对3'末端形成因子作用的理解仍在不断发展,最终情况可能比最初设想的更为复杂。