Uses of twins in studying the genetics of complex traits

Tim D. Spector, Alex J. MacGregor, Harold Snieder
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引用次数: 3

Abstract

Twins provide a useful and powerful tool for identifying genes, by acting as ideally matched sib-pairs, but are also uniquely placed to measure the extent of their action, their expression and the nature of their interaction with the environment. Classical twin studies have provided insight into the relative genetic and environmental contribution to characteristics and diseases in human populations. The search for a more detailed understanding of genetic mechanisms through linkage and association has, however, traditionally been regarded as the province of other family designs. The last few years have seen a resurgence of interest in twin research following an increasing awareness that the study of twins can also provide an important contribution to localizing and understanding the function of specific genes.1 In this brief overview, we focus on these newer developments that are currently being applied in the search to uncover the genetic basis of disease.
利用双胞胎研究复杂性状的遗传学
双胞胎作为理想匹配的兄弟姐妹,为识别基因提供了有用而有力的工具,但也具有独特的地位,可以衡量他们的行为程度、表达以及他们与环境相互作用的性质。经典的双胞胎研究提供了对人类群体特征和疾病的相对遗传和环境贡献的见解。然而,通过联系和关联寻找更详细的遗传机制,传统上被认为是其他家族设计的领域。最近几年,随着人们越来越意识到对双胞胎的研究也可以为定位和理解特定基因的功能做出重要贡献,人们对双胞胎研究的兴趣重新抬头在这篇简短的综述中,我们将重点介绍目前正在应用于揭示疾病遗传基础的研究中的这些新进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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