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Autosomal genetic control of human gene expression does not differ across the sexes.
Kassam, Irfahan; Lloyd-Jones, Luke; Holloway, Alexander; Small, Kerrin S; Zeng, Biao; Bakshi, Andrew; Metspalu, Andres; Gibson, Greg; Spector, Tim D; Esko, Tonu; Montgomery, Grant W; Powell, Joseph E; Yang, Jian; Visscher, Peter M; McRae, Allan F.
Afiliação
  • Kassam I; Queensland Brain Institute, The University of Queensland, Brisbane, Australia. i.kassam@uq.edu.au.
  • Lloyd-Jones L; Queensland Brain Institute, The University of Queensland, Brisbane, Australia.
  • Holloway A; Queensland Brain Institute, The University of Queensland, Brisbane, Australia.
  • Small KS; Department of Twin Research and Genetic Epidemiology, King's College London, London, UK.
  • Zeng B; School of Biology and Centre for Integrative Genomics, Georgia Institute of Technology, Atlanta, USA.
  • Bakshi A; Queensland Brain Institute, The University of Queensland, Brisbane, Australia.
  • Metspalu A; Estonian Genome Centre, University of Tartu, Tartu, Estonia.
  • Gibson G; School of Biology and Centre for Integrative Genomics, Georgia Institute of Technology, Atlanta, USA.
  • Spector TD; Department of Twin Research and Genetic Epidemiology, King's College London, London, UK.
  • Esko T; Estonian Genome Centre, University of Tartu, Tartu, Estonia.
  • Montgomery GW; Institute for Molecular Bioscience, University of Queensland, Brisbane, Australia.
  • Powell JE; QIMR Berghofer Medical Research Institute, Brisbane, Australia.
  • Yang J; Queensland Brain Institute, The University of Queensland, Brisbane, Australia.
  • Visscher PM; Institute for Molecular Bioscience, University of Queensland, Brisbane, Australia.
  • McRae AF; Queensland Brain Institute, The University of Queensland, Brisbane, Australia.
Genome Biol ; 17(1): 248, 2016 12 01.
Article em En | MEDLINE | ID: mdl-27908293
ABSTRACT

BACKGROUND:

Despite their nearly identical genomes, males and females differ in risk, incidence, prevalence, severity and age-at-onset of many diseases. Sexual dimorphism is also seen in human autosomal gene expression, and has largely been explored by examining the contribution of genotype-by-sex interactions to variation in gene expression.

RESULTS:

In this study, we use data from a mixture of pedigree and unrelated individuals with verified European ancestry to investigate the sex-specific genetic architecture of gene expression measured in whole blood across n=1048 males and n=1005 females by treating gene expression intensities in the sexes as two distinct traits and estimating the genetic correlation (r G) between them. These correlations measure the similarity of the combined additive genetic effects of all single-nucleotide polymorphisms across the autosomal chromosomes, and thus the level of common genetic control of gene expression across the sexes. Genetic correlations are estimated across the sexes for the expression levels of 12,528 autosomal gene expression probes using bivariate GREML, and tested for differences in autosomal genetic control of gene expression across the sexes. Overall, no deviation of the distribution of test statistics is observed from that expected under the null hypothesis of a common autosomal genetic architecture for gene expression across the sexes.

CONCLUSIONS:

These results suggest that males and females share the same common genetic control of gene expression.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Regulação da Expressão Gênica / Caracteres Sexuais / Genótipo Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Regulação da Expressão Gênica / Caracteres Sexuais / Genótipo Idioma: En Ano de publicação: 2016 Tipo de documento: Article