Department of Cognitive, Linguistic and Psychological Sciences, Brown Institute for Brain Science, Brown University, Providence, RI 02912-1978, USA.
Neuropsychopharmacology. 2011 Jan;36(1):133-52. doi: 10.1038/npp.2010.96. Epub 2010 Jul 14.
Many of the individual differences in cognition, motivation, and learning-and the disruption of these processes in neurological conditions-are influenced by genetic factors. We provide an integrative synthesis across human and animal studies, focusing on a recent spate of evidence implicating a role for genes controlling dopaminergic function in frontostriatal circuitry, including COMT, DARPP-32, DAT1, DRD2, and DRD4. These genetic effects are interpreted within theoretical frameworks developed in the context of the broader cognitive and computational neuroscience literature, constrained by data from pharmacological, neuroimaging, electrophysiological, and patient studies. In this framework, genes modulate the efficacy of particular neural computations, and effects of genetic variation are revealed by assays designed to be maximally sensitive to these computations. We discuss the merits and caveats of this approach and outline a number of novel candidate genes of interest for future study.
许多认知、动机和学习方面的个体差异,以及神经疾病中这些过程的中断,都受到遗传因素的影响。我们在人类和动物研究中提供了一个综合的综合分析,重点是最近一系列证据表明,控制多巴胺能功能的基因在额纹体电路中起作用,包括 COMT、DARPP-32、DAT1、DRD2 和 DRD4。这些遗传效应是在更广泛的认知和计算神经科学文献背景下发展的理论框架内解释的,受来自药理学、神经影像学、电生理学和患者研究的数据的限制。在这个框架中,基因调节特定神经计算的功效,并且通过设计为对这些计算最敏感的测定来揭示遗传变异的影响。我们讨论了这种方法的优点和注意事项,并概述了一些未来研究中感兴趣的新候选基因。