Genome-wide Screening for DNA Variants Associated with Reading and Language Traits

Authors

• A. Gialluisi, Max Planck Institute for Psycholinguistics
• D. F. Newbury, Wellcome Trust Centre for Human Genetics, University of Oxford
• E. G. Wilcutt, University of Colorado, Boulder
• R. K. Olson, University of Colorado, Boulder
• J. C. DeFries, University of Colorado, Boulder
• W. M. Brandler, University of Oxford
• Bruce F. Pennington, University of DenverFollow
• S. D. Smith, University of Nebraska Medical Center
• T. S. Scerri, The Walter and Eliza Hall Institute of Medical Research
• N. H. Simpson, Wellcome Trust Centre for Human Genetics, University of Oxford
• M. Luciano, University of Edinburgh
• D. M. Evans, University of Bristol, University of Queensland Diamantina Institute
• T. C. Bates, University of Edinburgh, Queensland Institute of Medical Research
• J. F. Stein, University of Oxford
• J. B. Talcott, Aston University
• A. P. Monaco, University of Oxford, Tufts University
• S. Paracchini, University of St Andrews
• C. Francks, Max Planck Institute for Psycholinguistics, Donders Institute for Brain, Cognition & Behavior,
• S. E. Fisher, Max Planck Institute for Psycholinguistics, Donders Institute for Brain, Cognition & Behavior,

Publication Date

7-28-2014

Document Type

Article

Organizational Units

College of Arts Humanities and Social Sciences, Psychology

Keywords

CLDRC, Developmental dyslexia, GWAS, Language, Meta‐analysis, Pleiotropic variants, Reading, Reading disability, SLIC, Specific language impairment

Abstract

Reading and language abilities are heritable traits that are likely to share some genetic influences with each other. To identify pleiotropic genetic variants affecting these traits, we first performed a genome-wide association scan (GWAS) meta-analysis using three richly characterized datasets comprising individuals with histories of reading or language problems, and their siblings. GWAS was performed in a total of 1862 participants using the first principal component computed from several quantitative measures of reading- and language-related abilities, both before and after adjustment for performance IQ. We identified novel suggestive associations at the SNPs rs59197085 and rs5995177 (uncorrected P ≈ 10-7 for each SNP), located respectively at the CCDC136/ FLNC and RBFOX2 genes. Each of these SNPs then showed evidence for effects across multiple reading and language traits in univariate association testing against the individual traits. FLNC encodes a structural protein involved in cytoskeleton remodelling, while RBFOX2 is an important regulator of alternative splicing in neurons. The CCDC136/FLNC locus showed association with a comparable reading/language measure in an independent sample of 6434 participants from the general population, although involving distinct alleles of the associated SNP. Our datasets will form an important part of on-going international efforts to identify genes contributing to reading and language skills.

Copyright Date

7-28-2014

Copyright Statement / License for Reuse

This work is licensed under a Creative Commons Attribution 4.0 International License.

Rights Holder

The Authors

Provenance

Received from author

Language

English (eng)

Extent

25 pgs

Publication Statement

Copyright held by the authors. Genes, Brain and Behavior published by International Behavioural and Neural Genetics Society and John Wiley & Sons Ltd. User is responsible for all copyright compliance.

Publication Title

Genes, Brain and Behavior

Volume

13

Issue

7

First Page

686

Last Page

701

ISSN

1601-183X

Recommended Citation

Gialluisi, A., Newbury, D. F., Wilcutt, E. G., Olson, R. K., DeFries, J. C., Brandler, W. M., . . . & Fisher, S. E. (2014). Genome-wide screening for DNA variants associated with reading and language traits. Genes, Brain and Behavior, 13(7), 686-701. DOI: 10.1111/gbb.12158

DOI Link

https://doi.org/10.1111/gbb.12158