Patrick Kristin L, Ryan Colm J, Xu Jiewei, Lipp Jesse J, Nissen Kelly E, Roguev Assen, Shales Michael, Krogan Nevan J, Guthrie Christine
Department of Biochemistry and Biophysics, University of California, San Francisco, California, United States of America.
Systems Biology Ireland, University College Dublin, Dublin, Ireland; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, California, United States of America; California Institute for Quantitative Biosciences, QB3, San Francisco, California, United States of America.
PLoS Genet. 2015 Mar 31;11(3):e1005074. doi: 10.1371/journal.pgen.1005074. eCollection 2015 Mar.
Although numerous regulatory connections between pre-mRNA splicing and chromatin have been demonstrated, the precise mechanisms by which chromatin factors influence spliceosome assembly and/or catalysis remain unclear. To probe the genetic network of pre-mRNA splicing in the fission yeast Schizosaccharomyces pombe, we constructed an epistatic mini-array profile (E-MAP) and discovered many new connections between chromatin and splicing. Notably, the nucleosome remodeler SWI/SNF had strong genetic interactions with components of the U2 snRNP SF3 complex. Overexpression of SF3 components in ΔSWI/SNF cells led to inefficient splicing of many fission yeast introns, predominantly those with non-consensus splice sites. Deletion of SWI/SNF decreased recruitment of the splicing ATPase Prp2, suggesting that SWI/SNF promotes co-transcriptional spliceosome assembly prior to first step catalysis. Importantly, defects in SWI/SNF as well as SF3 overexpression each altered nucleosome occupancy along intron-containing genes, illustrating that the chromatin landscape both affects--and is affected by--co-transcriptional splicing.
尽管已经证明了前体mRNA剪接与染色质之间存在众多调控联系,但染色质因子影响剪接体组装和/或催化的精确机制仍不清楚。为了探究裂殖酵母粟酒裂殖酵母中前体mRNA剪接的遗传网络,我们构建了一个上位性微阵列图谱(E-MAP),并发现了染色质与剪接之间的许多新联系。值得注意的是,核小体重塑因子SWI/SNF与U2 snRNP SF3复合体的组分有很强的遗传相互作用。在ΔSWI/SNF细胞中过表达SF3组分导致许多裂殖酵母内含子剪接效率低下,主要是那些具有非共有剪接位点的内含子。缺失SWI/SNF会减少剪接ATP酶Prp2的募集,这表明SWI/SNF在第一步催化之前促进共转录剪接体组装。重要的是,SWI/SNF的缺陷以及SF3的过表达都会改变含内含子基因上的核小体占有率,这说明染色质格局既影响共转录剪接,又受共转录剪接的影响。