Department of Neurology, University of Kentucky, Lexington, Kentucky, United States of America.
PLoS One. 2012;7(12):e51266. doi: 10.1371/journal.pone.0051266. Epub 2012 Dec 17.
In this study, we have investigated the global impact of heterogeneous nuclear Ribonuclear Protein (hnRNP) H/F-mediated regulation of splicing events and gene expression in oligodendrocytes. We have performed a genome-wide transcriptomic analysis at the gene and exon levels in Oli-neu cells treated with siRNA that targets hnRNPH/F compared to untreated cells using Affymetrix Exon Array. Gene expression levels and regulated exons were identified with the GenoSplice EASANA algorithm. Bioinformatics analyses were performed to determine the structural properties of G tracts that correlate with the function of hnRNPH/F as enhancers vs. repressors of exon inclusion. Different types of alternatively spliced events are regulated by hnRNPH/F. Intronic G tracts density, length and proximity to the 5' splice site correlate with the hnRNPH/F enhancer function. Additionally, 6% of genes are differently expressed upon knock down of hnRNPH/F. Genes that regulate the transition of oligodendrocyte progenitor cells to oligodendrocytes are differentially expressed in hnRNPH/F depleted Oli-neu cells, resulting in a decrease of negative regulators and an increase of differentiation-inducing regulators. The changes were confirmed in developing oligodendrocytes in vivo. This is the first genome wide analysis of splicing events and gene expression regulated by hnRNPH/F in oligodendrocytes and the first report that hnRNPH/F regulate genes that are involved in the transition from oligodendrocyte progenitor cells to oligodendrocytes.
在这项研究中,我们研究了异质核核糖核蛋白(hnRNP)H/F 介导的剪接事件和基因表达在少突胶质细胞中的全局影响。我们通过 Affymetrix Exon Array 在 Oli-neu 细胞中进行了全基因组转录组分析,该细胞用靶向 hnRNPH/F 的 siRNA 处理,与未处理的细胞相比,使用 GenoSplice EASANA 算法鉴定基因表达水平和调节外显子。生物信息学分析用于确定与 hnRNPH/F 作为增强子与内含子的功能相关的 G 带的结构特性。不同类型的可变剪接事件受 hnRNPH/F 调节。内含子 G 带密度、长度和与 5'剪接位点的接近程度与 hnRNPH/F 增强子功能相关。此外,hnRNPH/F 敲低后有 6%的基因表达水平不同。调节少突胶质细胞前体细胞向少突胶质细胞转化的基因在 hnRNPH/F 耗尽的 Oli-neu 细胞中表达不同,导致负调控因子减少,诱导分化的调控因子增加。这些变化在体内发育中的少突胶质细胞中得到了证实。这是 hnRNPH/F 调控少突胶质细胞剪接事件和基因表达的全基因组分析的首次报道,也是 hnRNPH/F 调控参与少突胶质细胞前体细胞向少突胶质细胞转化的基因的首次报道。