首页> 美国卫生研究院文献>PLoS Clinical Trials >Global Profiling of Alternative Splicing Events and Gene Expression Regulated by hnRNPH/F
【2h】

Global Profiling of Alternative Splicing Events and Gene Expression Regulated by hnRNPH/F

机译:hnRNPH / F调控的选择性剪接事件和基因表达的全球分析

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

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.
机译:在这项研究中,我们已经调查了异质核核糖核蛋白(hnRNP)H / F介导的剪接事件和少突胶质细胞基因表达调控的全球影响。与使用Affymetrix外显子阵列未处理的细胞相比,我们用针对hnRNPH / F的siRNA处理的Oli-neu细胞的基因和外显子水平进行了全基因组转录组分析。基因表达水平和受调控的外显子用GenoSplice EASANA算法鉴定。进行了生物信息学分析,以确定与hnRNPH / F作为外显子包涵体的增强子和阻遏子的功能相关的G道的结构特性。 hnRNPH / F调节不同类型的可变剪接事件。内含子G的密度,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,敲低hnRNPH / F后,有6%的基因表达不同。在hnRNPH / F缺失的Oli-neu细胞中差异表达调控少突胶质祖细胞向少突胶质细胞过渡的基因,从而导致负调控因子的减少和诱导分化的调控因子的增加。在体内发育中的少突胶质细胞中证实了这种变化。这是第一次基因组范围内的剪接事件和hnRNPH / F在少突胶质细胞中调节的基因表达的全基因组分析,并且是第一个报道hnRNPH / F调节从少突胶质祖细胞到少​​突胶质细胞转化的基因。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号