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遗传和表观遗传变异对基因调控和剪接的组织特异性影响。

Tissue-specific effects of genetic and epigenetic variation on gene regulation and splicing.

作者信息

Gutierrez-Arcelus Maria, Ongen Halit, Lappalainen Tuuli, Montgomery Stephen B, Buil Alfonso, Yurovsky Alisa, Bryois Julien, Padioleau Ismael, Romano Luciana, Planchon Alexandra, Falconnet Emilie, Bielser Deborah, Gagnebin Maryline, Giger Thomas, Borel Christelle, Letourneau Audrey, Makrythanasis Periklis, Guipponi Michel, Gehrig Corinne, Antonarakis Stylianos E, Dermitzakis Emmanouil T

机构信息

Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, Switzerland; Institute of Genetics and Genomics in Geneva (iGE3), Geneva, Switzerland; Swiss Institute of Bioinformatics (SIB), Geneva, Switzerland.

Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, Switzerland; Departments of Pathology and Genetics, Stanford University, Stanford, California, United States of America.

出版信息

PLoS Genet. 2015 Jan 29;11(1):e1004958. doi: 10.1371/journal.pgen.1004958. eCollection 2015 Jan.

Abstract

Understanding how genetic variation affects distinct cellular phenotypes, such as gene expression levels, alternative splicing and DNA methylation levels, is essential for better understanding of complex diseases and traits. Furthermore, how inter-individual variation of DNA methylation is associated to gene expression is just starting to be studied. In this study, we use the GenCord cohort of 204 newborn Europeans' lymphoblastoid cell lines, T-cells and fibroblasts derived from umbilical cords. The samples were previously genotyped for 2.5 million SNPs, mRNA-sequenced, and assayed for methylation levels in 482,421 CpG sites. We observe that methylation sites associated to expression levels are enriched in enhancers, gene bodies and CpG island shores. We show that while the correlation between DNA methylation and gene expression can be positive or negative, it is very consistent across cell-types. However, this epigenetic association to gene expression appears more tissue-specific than the genetic effects on gene expression or DNA methylation (observed in both sharing estimations based on P-values and effect size correlations between cell-types). This predominance of genetic effects can also be reflected by the observation that allele specific expression differences between individuals dominate over tissue-specific effects. Additionally, we discover genetic effects on alternative splicing and interestingly, a large amount of DNA methylation correlating to alternative splicing, both in a tissue-specific manner. The locations of the SNPs and methylation sites involved in these associations highlight the participation of promoter proximal and distant regulatory regions on alternative splicing. Overall, our results provide high-resolution analyses showing how genome sequence variation has a broad effect on cellular phenotypes across cell-types, whereas epigenetic factors provide a secondary layer of variation that is more tissue-specific. Furthermore, the details of how this tissue-specificity may vary across inter-relations of molecular traits, and where these are occurring, can yield further insights into gene regulation and cellular biology as a whole.

摘要

了解基因变异如何影响不同的细胞表型,如基因表达水平、可变剪接和DNA甲基化水平,对于更好地理解复杂疾病和性状至关重要。此外,DNA甲基化的个体间变异与基因表达之间的关联刚刚开始被研究。在本研究中,我们使用了GenCord队列,该队列包含204个欧洲新生儿的淋巴母细胞系、T细胞和成纤维细胞,这些细胞均来源于脐带。这些样本之前已针对250万个单核苷酸多态性(SNP)进行了基因分型、进行了mRNA测序,并对482421个CpG位点的甲基化水平进行了检测。我们观察到,与表达水平相关的甲基化位点在增强子、基因体和CpG岛岸中富集。我们发现,虽然DNA甲基化与基因表达之间的相关性可以是正的或负的,但在不同细胞类型中非常一致。然而,这种与基因表达的表观遗传关联似乎比基因对基因表达或DNA甲基化的影响更具组织特异性(在基于P值的共享估计以及细胞类型之间的效应大小相关性中均有观察到)。这种基因效应的主导地位也可以通过以下观察结果得到反映:个体之间的等位基因特异性表达差异比组织特异性效应更为显著。此外,我们发现了基因对可变剪接的影响,有趣的是,大量的DNA甲基化与可变剪接相关,且均以组织特异性的方式存在。参与这些关联中的SNP和甲基化位点的位置突出了启动子近端和远端调控区域在可变剪接中的作用。总体而言,我们的结果提供了高分辨率分析,显示了基因组序列变异如何对不同细胞类型的细胞表型产生广泛影响,而表观遗传因素则提供了一个更具组织特异性的二级变异层。此外,这种组织特异性在分子性状的相互关系中如何变化以及发生在哪里的细节,可以为整体的基因调控和细胞生物学提供进一步的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1243/4310612/88f684cdbf27/pgen.1004958.g001.jpg

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