Matveeva Elena, Maiorano John, Zhang Qingyang, Eteleeb Abdallah M, Convertini Paolo, Chen Jing, Infantino Vittoria, Stamm Stefan, Wang Jiping, Rouchka Eric C, Fondufe-Mittendorf Yvonne N
Department of Molecular and Cellular Biochemistry, University of Kentucky , Lexington, KY, USA.
Department of Molecular Biosciences, Northwestern University , Evanston, IL, USA.
Cell Discov. 2016 Feb 16;2:15046. doi: 10.1038/celldisc.2015.46. eCollection 2016.
Specialized chromatin structures such as nucleosomes with specific histone modifications decorate exons in eukaryotic genomes, suggesting a functional connection between chromatin organization and the regulation of pre-mRNA splicing. Through profiling the functional location of Poly (ADP) ribose polymerase, we observed that it is associated with the nucleosomes at exon/intron boundaries of specific genes, suggestive of a role for this enzyme in alternative splicing. Poly (ADP) ribose polymerase has previously been implicated in the PARylation of splicing factors as well as regulation of the histone modification H3K4me3, a mark critical for co-transcriptional splicing. In light of these studies, we hypothesized that interaction of the chromatin-modifying factor, Poly (ADP) ribose polymerase with nucleosomal structures at exon-intron boundaries, might regulate pre-mRNA splicing. Using genome-wide approaches validated by gene-specific assays, we show that depletion of PARP1 or inhibition of its PARylation activity results in changes in alternative splicing of a specific subset of genes. Furthermore, we observed that PARP1 bound to RNA, splicing factors and chromatin, suggesting that Poly (ADP) ribose polymerase serves as a gene regulatory hub to facilitate co-transcriptional splicing. These studies add another function to the multi-functional protein, Poly (ADP) ribose polymerase, and provide a platform for further investigation of this protein's function in organizing chromatin during gene regulatory processes.
诸如具有特定组蛋白修饰的核小体等特殊染色质结构修饰真核生物基因组中的外显子,这表明染色质组织与前体mRNA剪接调控之间存在功能联系。通过分析聚(ADP)核糖聚合酶的功能定位,我们观察到它与特定基因的外显子/内含子边界处的核小体相关,这表明该酶在可变剪接中发挥作用。聚(ADP)核糖聚合酶先前已被证明与剪接因子的聚ADP核糖基化以及组蛋白修饰H3K4me3的调控有关,H3K4me3是共转录剪接的关键标记。鉴于这些研究,我们推测染色质修饰因子聚(ADP)核糖聚合酶与外显子-内含子边界处的核小体结构的相互作用可能调节前体mRNA剪接。使用经基因特异性检测验证的全基因组方法,我们表明PARP1的缺失或其聚ADP核糖基化活性的抑制会导致特定基因子集的可变剪接发生变化。此外,我们观察到PARP1与RNA、剪接因子和染色质结合,这表明聚(ADP)核糖聚合酶作为一个基因调控枢纽促进共转录剪接。这些研究为多功能蛋白聚(ADP)核糖聚合酶增添了另一项功能,并为进一步研究该蛋白在基因调控过程中组织染色质的功能提供了一个平台。