Allayee Hooman, Ghazalpour Anatole, Lusis Aldons J
Department of Human Genetics, David Geffen School of Medicine at UCLA, USA.
Arterioscler Thromb Vasc Biol. 2003 Sep 1;23(9):1501-9. doi: 10.1161/01.ATV.0000090886.40027.DC. Epub 2003 Aug 14.
The genes that contribute to common, complex forms of atherosclerosis remain largely unknown. Genetic studies in humans have, for the most part, focused on identifying genes that predispose to the traditional risk factors, such as lipid levels and blood pressure, but apart from rare, single-gene disorders, there have been few successes to date. The use of mice to dissect the complex genetic etiology of atherosclerosis offers a viable alternative to human studies, because experimental parameters, such as environment, breeding scheme, and detailed phenotyping, can be controlled. Herein we review how mouse genetics can lead to the identification of genes, some of which would otherwise not have been considered as candidates for atherosclerosis, and provide an overview of the prospects for successful gene discovery in the future.
导致常见、复杂形式动脉粥样硬化的基因在很大程度上仍然未知。人类遗传学研究大多集中于识别易患传统风险因素(如血脂水平和血压)的基因,但除了罕见的单基因疾病外,迄今为止鲜有成功案例。利用小鼠剖析动脉粥样硬化复杂的遗传病因,为人类研究提供了一种可行的替代方法,因为诸如环境、育种方案和详细表型分析等实验参数可以得到控制。在此,我们综述了小鼠遗传学如何能够促成基因的识别,其中一些基因原本不会被视为动脉粥样硬化的候选基因,并概述了未来成功发现基因的前景。