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Common Regulatory Variation Impacts Gene Expression in a Cell Type-Dependent Manner

机译:常见的监管变异影响基因表达的细胞类型依赖性。

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摘要

Studies correlating genetic variation to gene expression facilitate the interpretation of common human phenotypes and disease. As functional variants may be operating in a tissue-dependent manner, we performed gene expression profiling and association with genetic variants (single-nucleotide polymorphisms) on three cell types of 75 individuals. We detected cell type-specific genetic effects, with 69 to 80% of regulatory variants operating in a cell type-specific manner, and identified multiple expressive quantitative trait loci (eQTLs) per gene, unique or shared among cell types and positively correlated with the number of transcripts per gene. Cell type-specific eQTLs were found at larger distances from genes and at lower effect size, similar to known enhancers. These data suggest that the complete regulatory variant repertoire can only be uncovered in the context of cell-type specificity.
机译:将遗传变异与基因表达相关联的研究有助于解释人类常见的表型和疾病。由于功能性变异可能以组织依赖性方式起作用,因此我们对75个个体的三种细胞类型进行了基因表达谱分析,并与遗传变异(单核苷酸多态性)相关联。我们检测了特定于细胞类型的遗传效应,其中69%至80%的调控变体以特定于细胞类型的方式运行,并确定了每个基因的多个表达性状特征位点(eQTL),它们在细胞类型之间是唯一的或共享的,并且与每个基因的转录本数量。发现与细胞类型相关的eQTL位于距基因较远,效应大小较小的位置,类似于已知的增强子。这些数据表明,仅在细胞类型特异性的背景下才能发现完整的调控变异体。

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  • 来源
    《Science》 |2009年第5945期|1246-1250|共5页
  • 作者单位

    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, CB10 1HH, Cambridge, UK;

    Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, CH-1211, Switzerland;

    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, CB10 1HH, Cambridge, UK Division of Genetics, Department of Medicine, Harvard Medical School and Brigham and Women's Hospital, Boston, MA, 02115 USA;

    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, CB10 1HH, Cambridge, UK;

    Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, CH-1211, Switzerland;

    Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, CH-1211, Switzerland;

    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, CB10 1HH, Cambridge, UK;

    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, CB10 1HH, Cambridge, UK;

    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, CB10 1HH, Cambridge, UK;

    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, CB10 1HH, Cambridge, UK;

    Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, CH-1211, Switzerland;

    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, CB10 1HH, Cambridge, UK;

    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, CB10 1HH, Cambridge, UK;

    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, CB10 1HH, Cambridge, UK Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, CH-1211, Switzerland;

    Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, CH-1211, Switzerland;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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