Owen M J, Craddock N
Department of Psychological Medicine, University of Wales College of Medicine, Cardiff, UK.
Mol Psychiatry. 1996 Mar;1(1):21-6.
The majority of common psychiatric disorders pose problems for geneticists because of their complex and non-Mendelian modes of inheritance. Early attempts to map genes for mental illness have so far largely overlooked this and sought genes of major effect in multiplex families using the lod score method of linkage analysis. However it seems that major genes are likely to be at best rare causes of common mental disorders, and the majority of cases probably reflect the interaction of several and perhaps many genes of comparatively small effect. There are two complementary sets of strategies that allow such genes to be identified. The first is to perform linkage analysis based on allele sharing in pairs of affected relatives. The second is to carry out association studies on samples of unrelated individuals. These methods and their applicability to psychiatric disorders are described. Psychiatric genetics has traditionally focussed on categorical phenotypes, but if valid continuous measures can be developed, powerful quantitative trait loci (QTL) approaches may also become feasible. Another important area is likely to be the study of relevant models in animals such as rodents in which genetic studies have many advantages. Finally we should not overlook the possibility that there are molecular explanations for irregular patterns of transmission such as mitochondrial inheritance, genomic imprinting and dynamic mutations.
大多数常见精神障碍给遗传学家带来了难题,因为它们具有复杂的、非孟德尔式的遗传模式。早期绘制精神疾病基因图谱的尝试大多忽略了这一点,而是使用连锁分析的对数优势计分法在多个患病家族中寻找具有主要作用的基因。然而,主要基因似乎充其量只是常见精神障碍的罕见病因,大多数病例可能反映了几个或许许多效应相对较小的基因之间的相互作用。有两套互补的策略可用于识别此类基因。第一种是基于患病亲属对之间的等位基因共享进行连锁分析。第二种是对无关个体样本进行关联研究。本文描述了这些方法及其在精神障碍中的适用性。传统上,精神遗传学专注于分类表型,但如果能够开发出有效的连续测量方法,强大的数量性状位点(QTL)方法也可能变得可行。另一个重要领域可能是对啮齿动物等动物的相关模型进行研究,在这些动物中进行遗传学研究有许多优势。最后,我们不应忽视这样一种可能性,即对于线粒体遗传、基因组印记和动态突变等不规则遗传模式存在分子解释。