Fisher Simon E, Francks Clyde
Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford, OX3 7BN, UK.
Trends Cogn Sci. 2006 Jun;10(6):250-7. doi: 10.1016/j.tics.2006.04.003. Epub 2006 May 3.
Studies of dyslexia provide vital insights into the cognitive architecture underpinning both disordered and normal reading. It is well established that inherited factors contribute to dyslexia susceptibility, but only very recently has evidence emerged to implicate specific candidate genes. In this article, we provide an accessible overview of four prominent examples--DYX1C1, KIAA0319, DCDC2 and ROBO1--and discuss their relevance for cognition. In each case correlations have been found between genetic variation and reading impairments, but precise risk variants remain elusive. Although none of these genes is specific to reading-related neuronal circuits, or even to the human brain, they have intriguing roles in neuronal migration or connectivity. Dissection of cognitive mechanisms that subserve reading will ultimately depend on an integrated approach, uniting data from genetic investigations, behavioural studies and neuroimaging.
诵读困难症的研究为理解支撑紊乱和正常阅读的认知结构提供了至关重要的见解。遗传因素导致诵读困难易感性这一点已得到充分证实,但直到最近才有证据表明某些特定的候选基因与之相关。在本文中,我们对四个突出的例子——DYX1C1、KIAA0319、DCDC2和ROBO1——进行了通俗易懂的概述,并讨论了它们与认知的相关性。在每种情况下,都发现了基因变异与阅读障碍之间的关联,但精确的风险变异仍难以捉摸。尽管这些基因都不是与阅读相关的神经回路所特有的,甚至也不是人类大脑所特有的,但它们在神经元迁移或连接中具有引人入胜的作用。对支持阅读的认知机制的剖析最终将依赖于一种综合方法,将来自基因研究、行为研究和神经成像的数据结合起来。