Association of Reading Disabilities With Regions Marked by Acetylated H3 Histones in KIAA0319

被引:44
作者
Couto, Jillian M. [1 ]
Livne-Bar, Izzy [1 ]
Huang, Katherine [1 ]
Xu, Zhaodong [1 ]
Cate-Carter, Tasha [2 ]
Feng, Yu [1 ]
Wigg, Karen [1 ]
Humphries, Tom [2 ]
Tannock, Rosemary [2 ]
Kerr, Elizabeth N. [2 ]
Lovett, Maureen W. [2 ]
Bremner, Rod [1 ]
Barr, Cathy L. [1 ,2 ]
机构
[1] Toronto Western Hosp, Toronto Western Res Inst, Univ Hlth Network, Genet & Dev Div, Toronto, ON M5T 2S8, Canada
[2] Hosp Sick Children, Program Neurosci & Mental Hlth, Toronto, ON M5G 1X8, Canada
关键词
reading disabilities; association; dyslexia; 6p; ChIP-chip; QUANTITATIVE-TRAIT LOCUS; DYSLEXIA SUSCEPTIBILITY LOCUS; CHROMOSOME 6P INFLUENCES; DEVELOPMENTAL DYSLEXIA; MAPPING PROVIDES; CANDIDATE GENES; LINKAGE; CHROMATIN; EXPRESSION; IDENTIFICATION;
D O I
10.1002/ajmg.b.30999
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Reading disabilities (RDs) have been associated with chromosome 6p with recent studies pointing to two genes, DCDC2 and KIAA0319. In this study, markers across the 6p region were tested for association with RD. Our strongest findings were for association with markers in KLA0319, although with the opposite alleles compared with a previous study. We also found association with markers in VMP, but not with DCDC2. Current evidence indicates that differential regulation of KIAA0319 and DCDC2 contributes to RD, thus we used chromatin immuno-precipitation coupled with genomic tiling arrays (ChIP-chip) to map acetylated histones, a molecular marker for regulatory elements, across a 500 kb genomic region covering the RD locus on 6p. This approach identified several regions marked by acetylated histones that mapped near associated markers, including intron 7 of DCDC2 and the 5' region of KIAA0319. The latter is located within the 70 kb region previously associated with differential expression of KIAA0319. Interestingly, five markers associated with RD in independent studies were also located within the 2.7kb acetylated region, and six additional associated markers, including the most significant one in this study, were located within a 22 kb haplotype block that encompassed this region. Our data indicates that this putative regulatory region is a likely site of genetic variation contributing to RD in our sample, further narrowing the candidate region. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:447 / 462
页数:16
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