Bourgeois Cyril F, Lejeune Fabrice, Stévenin James
Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS/INSERM/ULP, 67404 Illkirch, C.U. Strasbourg, France.
Prog Nucleic Acid Res Mol Biol. 2004;78:37-88. doi: 10.1016/S0079-6603(04)78002-2.
Alternative splicing of pre-messenger RNA (pre-mRNA) is a highly regulated process that allows expansion of the potential of expression of the genome in higher eukaryotes and involves many factors. Among them, the family of the serine- and arginine-rich proteins (SR proteins) plays a pivotal role: it has essential functions during spliceosome assembly and also interacts with RNA regulatory sequences on the pre-mRNA as well as with multiple cofactors. Collectively, SR proteins, because of their capacity to recognize multiple RNA sequences with a broad specificity, are at the heart of the regulation pathways that lead to the choice of alternative splice sites. Moreover, a growing body of evidence shows that the mechanisms of splicing regulation are not limited to the basic involvement of cis- and trans-acting factors at the pre-mRNA level, but result from intricate pathways, initiated sometimes by stimuli that are external to the cell and integrate SR proteins (and other factors) within an extremely sophisticated network of molecular machines associated with one another. This review focuses on the molecular aspects of the functions of SR proteins. In particular, we discuss the different ways in which SR proteins manage to achieve a high level of specificity in splicing regulation, even though they are also involved in the constitutive reaction.
前体信使RNA(pre-mRNA)的可变剪接是一个受到高度调控的过程,它使得高等真核生物基因组的表达潜力得以扩展,并且涉及许多因子。其中,富含丝氨酸和精氨酸的蛋白质(SR蛋白)家族发挥着关键作用:它在剪接体组装过程中具有重要功能,还能与pre-mRNA上的RNA调控序列以及多种辅因子相互作用。总体而言,SR蛋白由于能够以广泛的特异性识别多种RNA序列,处于导致可变剪接位点选择的调控途径的核心位置。此外,越来越多的证据表明,剪接调控机制不仅限于顺式和反式作用因子在pre-mRNA水平的基本参与,而是源于复杂的途径,这些途径有时由细胞外部的刺激引发,并将SR蛋白(及其他因子)整合到一个彼此关联的极其复杂的分子机器网络中。本综述聚焦于SR蛋白功能的分子层面。特别地,我们讨论了SR蛋白在剪接调控中实现高度特异性的不同方式,尽管它们也参与组成型反应。