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Mice as a Mammalian Model for Research on the Genetics of Aging

机译:小鼠作为哺乳动物的衰老遗传学研究模型

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摘要

Mice are an ideal mammalian model for studying the genetics of aging: considerable resources are available, the generation time is short, and the environment can be easily controlled, an important consideration when performing mapping studies to identify genes that influence lifespan and age-related diseases. In this review we highlight some salient contributions of the mouse in aging research: lifespan intervention studies in the Interventions Testing Program of the National Institute on Aging; identification of the genetic underpinnings of the effects of calorie restriction on lifespan; the Aging Phenome Project at the Jackson Laboratory, which has submitted multiple large, freely available phenotyping datasets to the Mouse Phenome Database; insights from spontaneous and engineered mouse mutants; and complex traits analyses identifying quantitative trait loci that affect lifespan. We also show that genomewide association peaks for lifespan in humans and lifespan quantitative loci for mice map to homologous locations in the genome. Thus, the vast bioinformatic and genetic resources of the mouse can be used to screen candidate genes identified in both mouse and human mapping studies, followed by functional testing, often not possible in humans, to determine their influence on aging.
机译:小鼠是研究衰老遗传学的理想哺乳动物模型:可利用的资源很多,世代时间短,环境易于控制,这是进行定位研究以确定影响寿命和与年龄有关的疾病的基因时的重要考虑因素。在这篇综述中,我们重点介绍了鼠标在衰老研究中的一些显着贡献:美国国立衰老研究所的干预测试计划中的寿命干预研究;查明限制卡路里影响寿命的遗传基础;杰克逊实验室(Jackson Laboratory)的老化现象项目(Aging Phenome Project),该项目已向老鼠现象数据库(Mouse Phenome Database)提交了多个免费的大型表型数据集;自发和工程小鼠突变体的见解;以及对复杂性状进行分析,确定影响寿命的数量性状基因座。我们还显示了人类寿命的全基因组关联峰和小鼠的寿命定量基因座映射到基因组中的同源位置。因此,小鼠的大量生物信息学和遗传资源可用于筛选在小鼠和人类作图研究中鉴定出的候选基因,然后进行功能测试(通常在人类中是不可能的),以确定它们对衰老的影响。

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