The genetic relationship between handedness and neurodevelopmental disorders

被引:106
作者
Brandler, William M. [1 ,2 ]
Paracchini, Silvia [3 ]
机构
[1] Univ Oxford, Dept Physiol Anat & Genet, MRC Funct Genom Unit, Oxford OX1 3PT, England
[2] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England
[3] Univ St Andrews, Sch Med, St Andrews KY16 9TF, Fife, Scotland
基金
英国惠康基金;
关键词
cerebral asymmetry; ciliogenesis; corpus callosum; dyslexia; handedness; schizophrenia; RELATIVE HAND SKILL; LEFT-RIGHT ASYMMETRY; MOTOR COORDINATION; LINKAGE ANALYSIS; BRAIN ASYMMETRY; SITUS-INVERSUS; APOE GENOTYPE; SINGLE-LOCUS; ASSOCIATION; SCHIZOPHRENIA;
D O I
10.1016/j.molmed.2013.10.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Handedness and brain asymmetry have been linked to neurodevelopmental disorders such as dyslexia and schizophrenia. The genetic nature of this correlation is not understood. Recent discoveries have shown handedness is determined in part by the biological pathways that establish left/right (LR) body asymmetry during development. Cilia play a key role in this process, and candidate genes for dyslexia have also been recently shown to be involved in cilia formation. Defective cilia result not only in LR body asymmetry phenotypes but also brain midline phenotypes such as an absent corpus callosum. These findings suggest that the mechanisms for establishing LR asymmetry in the body are reused for brain midline development, which in turn influences traits such as handedness and reading ability.
引用
收藏
页码:83 / 90
页数:8
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