Handedness and the X chromosome: The role of androgen receptor CAG-repeat length

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Larissa Arning - , Ruhr University Bochum (Author)
  • Sebastian Ocklenburg - , Ruhr University Bochum (Author)
  • Stefanie Schulz - , Ruhr University Bochum (Author)
  • Vanessa Ness - , Ruhr University Bochum (Author)
  • Wanda M. Gerding - , Ruhr University Bochum (Author)
  • Jan G. Hengstler - , Dortmund University of Technology (Author)
  • Michael Falkenstein - , Dortmund University of Technology (Author)
  • Jörg T. Epplen - , Ruhr University Bochum (Author)
  • Onur Güntürkün - , Ruhr University Bochum (Author)
  • Christian Beste - , Department of Child and Adolescent Psychiatry and Psychotherapy (Author)

Abstract

Prenatal androgen exposure has been suggested to be one of the factors influencing handedness, making the androgen receptor gene (AR) a likely candidate gene for individual differences in handedness. Here, we examined the relationship between the length of the CAG-repeat in AR and different handedness phenotypes in a sample of healthy adults of both sexes (n = 1057). Since AR is located on the X chromosome, statistical analyses in women heterozygous for CAG-repeat lengths are complicated by X chromosome inactivation. We thus analyzed a sample of women that were homozygous for the CAG-repeat length (n = 77). Mixed-handedness in men was significantly associated with longer CAG-repeat blocks and women homozygous for longer CAG-repeats showed a tendency for stronger left-handedness. These results suggest that handedness in both sexes is associated with the AR CAG-repeat length, with longer repeats being related to a higher incidence of non-right-handedness. Since longer CAG-repeat blocks have been linked to less efficient AR function, these results implicate that differences in AR signaling in the developing brain might be one of the factors that determine individual differences in brain lateralization.

Details

Original languageEnglish
Article number8325
Number of pages5
JournalScientific reports
Volume5
Publication statusPublished - Feb 2015
Peer-reviewedYes

External IDs

PubMed 25659367
ORCID /0000-0002-2989-9561/work/160952552

Keywords

ASJC Scopus subject areas