A dyslexia-associated variant in DCDC2 changes gene expression

Behav Genet. 2011 Jan;41(1):58-66. doi: 10.1007/s10519-010-9408-3. Epub 2010 Nov 2.

Abstract

Reading disability (RD) or dyslexia is a common neurogenetic disorder. Two genes, KIAA0319 and DCDC2, have been identified by association studies of the DYX2 locus on 6p21.3. We previously identified a 2445 bp deletion, and a compound STR within the deleted region (BV677278), in intron 2 of DCDC2. The deletion and several alleles of the STR are strongly associated with RD (P = 0.00002). In this study we investigated whether BV677278 is a regulatory region for DCDC2 by electrophoretic mobility shift and luciferase reporter assays. We show that oligonucleotide probes from the STR bind nuclear protein from human brain, and that alleles of the STR have a range of DCDC2-specific enhancer activities. Five alleles displayed strong enhancer activity and increased gene expression, while allele 1 showed no enhancer activity. These studies suggest that the association of BV677278 with RD reflects a role as a modifier of DCDC2 expression.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles*
  • Brain / metabolism
  • Cell Line
  • Chromosome Deletion
  • Dyslexia / genetics*
  • Electrophoretic Mobility Shift Assay
  • Enhancer Elements, Genetic
  • Gene Expression / genetics*
  • Genetic Linkage
  • Genetic Variation / genetics*
  • Humans
  • Introns / genetics
  • Microsatellite Repeats / genetics
  • Microtubule-Associated Proteins / genetics*
  • Oligonucleotide Probes
  • Regulatory Sequences, Nucleic Acid / genetics

Substances

  • DCDC2 protein, human
  • Microtubule-Associated Proteins
  • Oligonucleotide Probes