Jorde L B, Watkins W S, Bamshad M J
Department of Human Genetics, University of Utah Health Sciences Center, Salt Lake City, UT 84112, USA.
Hum Mol Genet. 2001 Oct 1;10(20):2199-207. doi: 10.1093/hmg/10.20.2199.
Studies of human genetic variation are making contributions in several key areas. Evolutionary genetic studies yield critical clues about the histories of human populations, and they provide substantial support for an African origin of modern humans. The analysis of genetic variation has formed a foundation for DNA-based forensic applications. And, as attention is focused on locating genes underlying complex diseases, it is becoming clear that a better understanding of genetic variation will help to guide gene-mapping efforts. Population genomics, the large-scale comparison of DNA sequences, is now beginning to provide new insights in these areas. We review some of the general patterns of human genetic variation, and we show how our knowledge of these patterns can aid in the mapping and cloning of disease-causing genes.
人类遗传变异研究在几个关键领域发挥着作用。进化遗传学研究为人类群体的历史提供了关键线索,并为现代人类起源于非洲提供了有力支持。遗传变异分析为基于DNA的法医应用奠定了基础。而且,随着人们将注意力集中在定位复杂疾病的潜在基因上,越来越清楚的是,更好地理解遗传变异将有助于指导基因定位工作。群体基因组学,即对DNA序列进行大规模比较,目前开始在这些领域提供新的见解。我们回顾了人类遗传变异的一些一般模式,并展示了我们对这些模式的了解如何有助于致病基因的定位和克隆。