Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals.

Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals.
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DOI:
10.1101/gr.155192.113
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发表时间:
2014-01
期刊:
影响因子:
7
通讯作者:
Koller D
Koller D
中科院分区:
生物学1区
文献类型:
--
作者:
Battle A;Mostafavi S;Zhu X;Potash JB;Weissman MM;McCormick C;Haudenschild CD;Beckman KB;Shi J;Mei R;Urban AE;Montgomery SB;Levinson DF;Koller D

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了解人类基因组中调控变异的后果仍然是一个重大挑战,对于理解基因调控和解释蛋白质编码区之外的许多疾病风险变异具有重要意义。在这里,我们通过对922个基因型个体的RNA进行测序,为遗传变异的调控后果提供了一个直接的窗口。我们提出了一个全面的描述的分布调节变异的特定表达表型改变,受影响的基因的属性,和基因组特征的调节变体。我们检测到影响一万多个基因表达的变异,并通过RNA测序提供的增强分辨率,我们首次鉴定出数千种与特定表型相关的变异,包括剪接和等位基因表达。评估两个远程染色体内和反式(跨染色体)调节的影响,我们观察到的调控网络中的模块化,三维染色体的配置在每个染色体内的调控模块中发挥特定的作用。我们还观察到影响中心和关键基因的调节变体的显著耗尽,沿着随着变体频率的增加效应大小减小的趋势,提供了纯化选择和缓冲限制了调节变体对细胞的有害影响的证据。此外,除了观察到的变异外,我们还分析了与表达和剪接相关的变异的基因组特性,并开发了贝叶斯模型来预测遗传变异的调控后果,适用于个体基因组和疾病研究的解释。总之,这些结果代表了表征人类调节变化的完整景观的关键一步。
Understanding the consequences of regulatory variation in the human genome remains a major challenge, with important implications for understanding gene regulation and interpreting the many disease-risk variants that fall outside of protein-coding regions. Here, we provide a direct window into the regulatory consequences of genetic variation by sequencing RNA from 922 genotyped individuals. We present a comprehensive description of the distribution of regulatory variation—by the specific expression phenotypes altered, the properties of affected genes, and the genomic characteristics of regulatory variants. We detect variants influencing expression of over ten thousand genes, and through the enhanced resolution offered by RNA-sequencing, for the first time we identify thousands of variants associated with specific phenotypes including splicing and allelic expression. Evaluating the effects of both long-range intra-chromosomal and trans (cross-chromosomal) regulation, we observe modularity in the regulatory network, with three-dimensional chromosomal configuration playing a particular role in regulatory modules within each chromosome. We also observe a significant depletion of regulatory variants affecting central and critical genes, along with a trend of reduced effect sizes as variant frequency increases, providing evidence that purifying selection and buffering have limited the deleterious impact of regulatory variation on the cell. Further, generalizing beyond observed variants, we have analyzed the genomic properties of variants associated with expression and splicing and developed a Bayesian model to predict regulatory consequences of genetic variants, applicable to the interpretation of individual genomes and disease studies. Together, these results represent a critical step toward characterizing the complete landscape of human regulatory variation.
DOI: 10.1186/gb-2003-4-3-r23
发表时间: 2003
期刊: Genome biology
影响因子: 12.3
作者:
Breitkreutz BJ;Stark C;Tyers M
通讯作者: Tyers M
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发表时间: 2011-09-11
期刊: NATURE
影响因子: 64.8
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发表时间: 2012-09
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