Literature DB >> 15717286

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.

Natalie Cope1, Denise Harold, Gary Hill, Valentina Moskvina, Jim Stevenson, Peter Holmans, Michael J Owen, Michael C O'Donovan, Julie Williams.   

Abstract

Linkage between developmental dyslexia (DD) and chromosome 6p has been replicated in a number of independent samples. Recent attempts to identify the gene responsible for the linkage have produced inconsistent evidence for association of DD with a number of genes in a 575-kb region of chromosome 6p22.2, including VMP, DCDC2, KIAA0319, TTRAP, and THEM2. We aimed to identify the specific gene or genes involved by performing a systematic, high-density (approximately 2-3-kb intervals) linkage disequilibrium screen of these genes in an independent sample, incorporating family-based and case-control designs in which dyslexia was defined as an extreme representation of reading disability. Using DNA pooling, we first observed evidence for association with 17 single-nucleotide polymorphisms (SNPs), 13 of which were located in the KIAA0319 gene (P<.01-.003). After redundant SNPs were excluded, 10 SNPs were individually genotyped in 223 subjects with DD and 273 controls. Those SNPs that were significant at P</=.05 were next genotyped in a semi-independent sample of 143 trios of probands with DD and their parents, to control for possible population stratification. Six SNPs showed significant evidence of association in both samples (P</=.04-.002), including a SNP (rs4504469) in exon 4 of the KIAA0319 gene that changes an amino acid (P=.002; odds ratio 1.5). Logistic regression analysis showed that two SNPs (rs4504469 and rs6935076) in the KIAA0319 gene best explained DD status. The haplotype composed of these two markers was significantly associated with DD (global P=.00001 in the case-control sample; P=.02 in trios). This finding was largely driven by underrepresentation of the most common haplotype in cases (P=.00003 in the case-control sample; P=.006 in trios; 1-degree-of-freedom tests). Our data strongly implicate KIAA0319 as a susceptibility gene for dyslexia. The gene product is expressed in brain, but its specific function is currently unknown.

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Year:  2005        PMID: 15717286      PMCID: PMC1199296          DOI: 10.1086/429131

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  46 in total

1.  Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q.

Authors:  D W Morris; L Robinson; D Turic; M Duke; V Webb; C Milham; E Hopkin; K Pound; S Fernando; M Easton; M Hamshere; N Williams; P McGuffin; J Stevenson; M Krawczak; M J Owen; M C O'Donovan; J Williams
Journal:  Hum Mol Genet       Date:  2000-03-22       Impact factor: 6.150

2.  Model-free analysis and permutation tests for allelic associations.

Authors:  J H Zhao; D Curtis; P C Sham
Journal:  Hum Hered       Date:  2000 Mar-Apr       Impact factor: 0.444

3.  Cloning, expression and characterization of a novel human VMP gene.

Authors:  Chao Cheng; Jian Xu; Xin Ye; Jianfeng Dai; Qihan Wu; Li Zeng; Liu Wang; Wei Zhao; Chaoneng Ji; Shaohua Gu; Yi Xie; Yumin Mao
Journal:  Mol Biol Rep       Date:  2002-09       Impact factor: 2.316

4.  The human mitochondrial Mrs2 protein functionally substitutes for its yeast homologue, a candidate magnesium transporter.

Authors:  G Zsurka; J Gregán; R J Schweyen
Journal:  Genomics       Date:  2001-03-01       Impact factor: 5.736

Review 5.  Visual function, fatty acids and dyslexia.

Authors:  K E Taylor; A J Richardson
Journal:  Prostaglandins Leukot Essent Fatty Acids       Date:  2000 Jul-Aug       Impact factor: 4.006

Review 6.  Fatty acid metabolism in neurodevelopmental disorder: a new perspective on associations between attention-deficit/hyperactivity disorder, dyslexia, dyspraxia and the autistic spectrum.

Authors:  A J Richardson; M A Ross
Journal:  Prostaglandins Leukot Essent Fatty Acids       Date:  2000 Jul-Aug       Impact factor: 4.006

7.  Fatty acid deficiency signs predict the severity of reading and related difficulties in dyslexic children.

Authors:  A J Richardson; C M Calvin; C Clisby; D R Schoenheimer; P Montgomery; J A Hall; G Hebb; E Westwood; J B Talcott; J F Stein
Journal:  Prostaglandins Leukot Essent Fatty Acids       Date:  2000 Jul-Aug       Impact factor: 4.006

8.  Chromosome 6p influences on different dyslexia-related cognitive processes: further confirmation.

Authors:  E L Grigorenko; F B Wood; M S Meyer; D L Pauls
Journal:  Am J Hum Genet       Date:  2000-02       Impact factor: 11.025

9.  TTRAP, a novel protein that associates with CD40, tumor necrosis factor (TNF) receptor-75 and TNF receptor-associated factors (TRAFs), and that inhibits nuclear factor-kappa B activation.

Authors:  S Pype; W Declercq; A Ibrahimi; C Michiels; J G Van Rietschoten; N Dewulf; M de Boer; P Vandenabeele; D Huylebroeck; J E Remacle
Journal:  J Biol Chem       Date:  2000-06-16       Impact factor: 5.157

10.  A new antigen recognized by cytolytic T lymphocytes on a human kidney tumor results from reverse strand transcription.

Authors:  B J Van Den Eynde; B Gaugler; M Probst-Kepper; L Michaux; O Devuyst; F Lorge; P Weynants; T Boon
Journal:  J Exp Med       Date:  1999-12-20       Impact factor: 14.307

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  103 in total

1.  Persistent spatial working memory deficits in rats following in utero RNAi of Dyx1c1.

Authors:  C E Szalkowski; J R Hinman; S W Threlkeld; Y Wang; A LePack; G D Rosen; J J Chrobak; J J LoTurco; R H Fitch
Journal:  Genes Brain Behav       Date:  2010-11-25       Impact factor: 3.449

2.  Neocortical disruption and behavioral impairments in rats following in utero RNAi of candidate dyslexia risk gene Kiaa0319.

Authors:  Caitlin E Szalkowski; Christopher G Fiondella; Albert M Galaburda; Glenn D Rosen; Joseph J Loturco; R Holly Fitch
Journal:  Int J Dev Neurosci       Date:  2012-02-03       Impact factor: 2.457

3.  Genetic variation in the KIAA0319 5' region as a possible contributor to dyslexia.

Authors:  Adrienne Elbert; Maureen W Lovett; Tasha Cate-Carter; Ashley Pitch; Elizabeth N Kerr; Cathy L Barr
Journal:  Behav Genet       Date:  2011-01-05       Impact factor: 2.805

4.  The effects of embryonic knockdown of the candidate dyslexia susceptibility gene homologue Dyx1c1 on the distribution of GABAergic neurons in the cerebral cortex.

Authors:  T A Currier; M A Etchegaray; J L Haight; A M Galaburda; G D Rosen
Journal:  Neuroscience       Date:  2010-11-09       Impact factor: 3.590

5.  Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.

Authors:  Jessica Becker; Darina Czamara; Tom S Scerri; Franck Ramus; Valéria Csépe; Joel B Talcott; John Stein; Andrew Morris; Kerstin U Ludwig; Per Hoffmann; Ferenc Honbolygó; Dénes Tóth; Fabien Fauchereau; Caroline Bogliotti; Stéphanie Iannuzzi; Yves Chaix; Sylviane Valdois; Catherine Billard; Florence George; Isabelle Soares-Boucaud; Christophe-Loïc Gérard; Sanne van der Mark; Enrico Schulz; Anniek Vaessen; Urs Maurer; Kaisa Lohvansuu; Heikki Lyytinen; Marco Zucchelli; Daniel Brandeis; Leo Blomert; Paavo H T Leppänen; Jennifer Bruder; Anthony P Monaco; Bertram Müller-Myhsok; Juha Kere; Karin Landerl; Markus M Nöthen; Gerd Schulte-Körne; Silvia Paracchini; Myriam Peyrard-Janvid; Johannes Schumacher
Journal:  Eur J Hum Genet       Date:  2013-09-11       Impact factor: 4.246

6.  DCDC2 is associated with reading disability and modulates neuronal development in the brain.

Authors:  Haiying Meng; Shelley D Smith; Karl Hager; Matthew Held; Jonathan Liu; Richard K Olson; Bruce F Pennington; John C DeFries; Joel Gelernter; Thomas O'Reilly-Pol; Stefan Somlo; Pawel Skudlarski; Sally E Shaywitz; Bennett A Shaywitz; Karen Marchione; Yu Wang; Murugan Paramasivam; Joseph J LoTurco; Grier P Page; Jeffrey R Gruen
Journal:  Proc Natl Acad Sci U S A       Date:  2005-11-08       Impact factor: 11.205

7.  Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region.

Authors:  K G Wigg; Y Feng; J Crosbie; R Tannock; J L Kennedy; A Ickowicz; M Malone; R Schachar; C L Barr
Journal:  Genes Brain Behav       Date:  2008-11       Impact factor: 3.449

8.  Meta-analysis of the association between DCDC2 polymorphisms and risk of dyslexia.

Authors:  Rong Zhong; Beifang Yang; Hui Tang; Li Zou; Ranran Song; Ling-Qiang Zhu; Xiaoping Miao
Journal:  Mol Neurobiol       Date:  2012-12-11       Impact factor: 5.590

9.  Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample.

Authors:  Kerstin U Ludwig; Darina Roeske; Johannes Schumacher; Gerd Schulte-Körne; Inke R König; Andreas Warnke; Ellen Plume; Andreas Ziegler; Helmut Remschmidt; Bertram Müller-Myhsok; Markus M Nöthen; Per Hoffmann
Journal:  J Neural Transm (Vienna)       Date:  2008-09-23       Impact factor: 3.575

10.  The effects of Kiaa0319 knockdown on cortical and subcortical anatomy in male rats.

Authors:  Caitlin E Szalkowski; Christopher F Fiondella; Dongnhu T Truong; Glenn D Rosen; Joseph J LoTurco; Roslyn H Fitch
Journal:  Int J Dev Neurosci       Date:  2012-12-05       Impact factor: 2.457

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