Modifier Genes and the Plasticity of Genetic Networks in Mice

被引:57
作者
Hamilton, Bruce A. [1 ,2 ,3 ]
Yu, Benjamin D. [2 ,3 ]
机构
[1] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Med, Moores UCSD Canc Ctr, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Inst Genom Med, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
CYSTIC-FIBROSIS; DILUTE SUPPRESSOR; GENOME-WIDE; COAT-COLOR; TRIALLELIC INHERITANCE; DISEASE SEVERITY; SPLICING FACTOR; MAJOR MODIFIER; COMPLEX TRAITS; MOUSE;
D O I
10.1371/journal.pgen.1002644
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Modifier genes are an integral part of the genetic landscape in both humans and experimental organisms, but have been less well explored in mammals than other systems. A growing number of modifier genes mouse models of disease nonetheless illustrate the potential for novel findings, while new technical advances promise many more to come. Modifier genes in mouse models include induced mutations and spontaneous or wild-derived variations captured in inbred strains. Identification of modifiers among wild-derived variants in particular should detect disease modifiers that have been shaped by selection and might therefore be compatible with high fitness and function. Here we review selected examples and argue that modifier genes derived from natural variation may provide a bias for nodes in genetic networks that have greater intrinsic plasticity and whose therapeutic manipulation may therefore be more resilient to side effects than conventional targets.
引用
收藏
页码:326 / 332
页数:7
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