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Time-dependent genetic effects on gene expression implicate aging processes.
Bryois, Julien; Buil, Alfonso; Ferreira, Pedro G; Panousis, Nikolaos I; Brown, Andrew A; Viñuela, Ana; Planchon, Alexandra; Bielser, Deborah; Small, Kerrin; Spector, Tim; Dermitzakis, Emmanouil T.
Afiliación
  • Bryois J; Department of Genetic Medicine and Development, University of Geneva Medical School, 1211 Geneva 4, Switzerland.
  • Buil A; Institute of Genetics and Genomics in Geneva (iGE3), 1211 Geneva 4, Switzerland.
  • Ferreira PG; Swiss Institute of Bioinformatics (SIB), 1211 Geneva 4, Switzerland.
  • Panousis NI; Department of Genetic Medicine and Development, University of Geneva Medical School, 1211 Geneva 4, Switzerland.
  • Brown AA; Institute of Genetics and Genomics in Geneva (iGE3), 1211 Geneva 4, Switzerland.
  • Viñuela A; Swiss Institute of Bioinformatics (SIB), 1211 Geneva 4, Switzerland.
  • Planchon A; Department of Genetic Medicine and Development, University of Geneva Medical School, 1211 Geneva 4, Switzerland.
  • Bielser D; Institute of Genetics and Genomics in Geneva (iGE3), 1211 Geneva 4, Switzerland.
  • Small K; Swiss Institute of Bioinformatics (SIB), 1211 Geneva 4, Switzerland.
  • Spector T; Department of Genetic Medicine and Development, University of Geneva Medical School, 1211 Geneva 4, Switzerland.
  • Dermitzakis ET; Institute of Genetics and Genomics in Geneva (iGE3), 1211 Geneva 4, Switzerland.
Genome Res ; 27(4): 545-552, 2017 04.
Article en En | MEDLINE | ID: mdl-28302734
ABSTRACT
Gene expression is dependent on genetic and environmental factors. In the last decade, a large body of research has significantly improved our understanding of the genetic architecture of gene expression. However, it remains unclear whether genetic effects on gene expression remain stable over time. Here, we show, using longitudinal whole-blood gene expression data from a twin cohort, that the genetic architecture of a subset of genes is unstable over time. In addition, we identified 2213 genes differentially expressed across time points that we linked with aging within and across studies. Interestingly, we discovered that most differentially expressed genes were affected by a subset of 77 putative causal genes. Finally, we observed that putative causal genes and down-regulated genes were affected by a loss of genetic control between time points. Taken together, our data suggest that instability in the genetic architecture of a subset of genes could lead to widespread effects on the transcriptome with an aging signature.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Envejecimiento / Regulación del Desarrollo de la Expresión Génica / Transcriptoma Tipo de estudio: Prognostic_studies Límite: Aged / Female / Humans / Middle aged Idioma: En Revista: Genome Res Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA Año: 2017 Tipo del documento: Article País de afiliación: Suiza

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Envejecimiento / Regulación del Desarrollo de la Expresión Génica / Transcriptoma Tipo de estudio: Prognostic_studies Límite: Aged / Female / Humans / Middle aged Idioma: En Revista: Genome Res Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA Año: 2017 Tipo del documento: Article País de afiliación: Suiza