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PCSK6 is associated with handedness in individuals with dyslexia
- Source :
- Human Molecular Genetics
- Publication Year :
- 2010
- Publisher :
- Oxford University Press, 2010.
-
Abstract
- Approximately 90% of humans are right-handed. Handedness is a heritable trait, yet the genetic basis is not well understood. Here we report a genome-wide association study for a quantitative measure of relative hand skill in individuals with dyslexia [reading disability (RD)]. The most highly associated marker, rs11855415 (P = 4.7 x 10(-7)), is located within PCSK6. Two independent cohorts with RD show the same trend, with the minor allele conferring greater relative right-hand skill. Meta-analysis of all three RD samples is genome-wide significant (n = 744, P = 2.0 x 10(-8)). Conversely, in the general population (n = 2666), we observe a trend towards reduced laterality of hand skill for the minor allele (P = 0.0020). These results provide molecular evidence that cerebral asymmetry and dyslexia are linked. Furthermore, PCSK6 is a protease that cleaves the left-right axis determining protein NODAL. Functional studies of PCSK6 promise insights into mechanisms underlying cerebral lateralization and dyslexia. Publisher PDF
- Subjects :
- Reading disability
REading-disability
Nodal Protein
Developmental dyslexia
Population
Genome-wide association study
QH426 Genetics
Biology
Susceptibility gene
Quantitative-trait locus
Functional Laterality
Relative hand skill
Dyslexia
03 medical and health sciences
0302 clinical medicine
Chromosome 6P
Genetics
medicine
Humans
Allele
education
Dominance, Cerebral
QH426
Molecular Biology
Genetics (clinical)
Language
030304 developmental biology
0303 health sciences
education.field_of_study
Genome-wide association
Association Studies Articles
Proteolytic enzymes
General Medicine
medicine.disease
United States
Minor allele frequency
Laterality
Linkage analysis
030217 neurology & neurosurgery
Genome-Wide Association Study
Subjects
Details
- Language :
- English
- ISSN :
- 14602083 and 09646906
- Volume :
- 20
- Issue :
- 3
- Database :
- OpenAIRE
- Journal :
- Human Molecular Genetics
- Accession number :
- edsair.doi.dedup.....fb2feccfdd30a3d949641523f4e2bbc3