4.8 Article

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.1017288108

Keywords

genome-wide analysis; epidemiologic; transcriptional expression analysis

Funding

  1. European Union [HEALTH-F4-2007-201413, LSHM-CT-2007-037286, 242257]
  2. United Kingdom National Institute for Health Research (NIHR) Biomedical Research Centre Mental Health, the Medical Research Council [93558]
  3. German Nationales Genomforschungsnetz [01GS08152]
  4. State of California for Medical Research through the University of California, San Francisco
  5. Research Council United Kingdom (RCUK)
  6. Imperial College Healthcare NHS Trust Comprehensive Biomedical Research Centre
  7. NIHR
  8. Swedish Council for Working Life and Social Research (FAS)
  9. Swedish Science Research Council
  10. Instituto de Salud Carlos III (ISCIII) [FIS PI021570]
  11. Junta de Castilla y Leon (JCyL) [SA044A08, GR93]
  12. RTICC, ISCIII, Spain [RD06/0020/000]
  13. MRC [MC_U106188470, G0601966, G0801056, G0700931, G0701863, G0901858, G0600676] Funding Source: UKRI
  14. Medical Research Council [G1000143, G0700931, G0801056, G0600676, MC_U106179471, MC_U106188470, G0901858, G0801056B, G0601966, G0701863, G9817803B, G0401527] Funding Source: researchfish

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Alcohol consumption is a moderately heritable trait, but the genetic basis in humans is largely unknown, despite its clinical and societal importance. We report a genome-wide association study meta-analysis of similar to 2.5 million directly genotyped or imputed SNPs with alcohol consumption (gram per day per kilogram body weight) among 12 population-based samples of European ancestry, comprising 26,316 individuals, with replication genotyping in an additional 21,185 individuals. SNP rs6943555 in autism susceptibility candidate 2 gene (AUTS2) was associated with alcohol consumption at genome-wide significance (P = 4 x 10(-8) to P = 4 x 10(-9)). We found a genotype-specific expression of AUTS2 in 96 human prefrontal cortex samples (P = 0.026) and significant (P < 0.017) differences in expression of AUTS2 in whole-brain extracts of mice selected for differences in voluntary alcohol consumption. Downregulation of an AUTS2 homolog caused reduced alcohol sensitivity in Drosophila (P < 0.001). Our finding of a regulator of alcohol consumption adds knowledge to our understanding of genetic mechanisms influencing alcohol drinking behavior.

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