Evolutionary mutant models for human disease

被引:90
作者
Albertson, R. Craig [1 ]
Cresko, William [2 ]
Detrich, H. William, III [3 ]
Postlethwait, John H. [4 ]
机构
[1] Syracuse Univ, Dept Biol, Syracuse, NY 13244 USA
[2] Univ Oregon, Ctr Ecol & Evolutionary Biol, Eugene, OR 97403 USA
[3] Northeastern Univ, Dept Biol, Boston, MA 02115 USA
[4] Univ Oregon, Inst Neurosci, Eugene, OR 97403 USA
基金
美国国家科学基金会;
关键词
EYE DEGENERATION; HETEROTOPIC OSSIFICATION; GENETIC-ANALYSIS; EXPRESSION; ZEBRAFISH; CAVEFISH; LIMB; PIGMENTATION; SEQUENCES; GENOMICS;
D O I
10.1016/j.tig.2008.11.006
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Although induced mutations in traditional laboratory animals have been valuable as models for human diseases, they have some important limitations. Here, we propose a complementary approach to discover genes and mechanisms that might contribute to human disorders: the analysis of evolutionary mutant models in which adaptive phenotypes mimic maladaptive human diseases. If the type and mode of action of mutations favored by natural selection in wild populations are similar to those that contribute to human diseases, then studies in evolutionary mutant models have the potential to identify novel genetic factors and gene-by environment interactions that affect human health and underlie human disease.
引用
收藏
页码:74 / 81
页数:8
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