From zebrafish to human: Modular medical models

被引:199
作者
Shin, JT [1 ]
Fishman, MC
机构
[1] Massachusetts Gen Hosp, Cardiovasc Res Ctr, Charlestown, MA 02129 USA
[2] Massachusetts Gen Hosp, Div Cardiol, Charlestown, MA 02129 USA
[3] Harvard Univ, Sch Med, Charlestown, MA 02129 USA
关键词
developmental biology; genetic screen; chemical screen; integrative physiology; pathophysiology;
D O I
10.1146/annurev.genom.3.031402.131506
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genetic screens in Drosophila melanogaster, Caenorhabditis elegans, and Danio rerio clarified the logic of metazoan development by revealing critical unitary steps and pathways to embryogenesis. Can genetic screens similarly organize medicine? We here examine human diseases that resemble mutations in Danio rerio, the zebrafish, the one vertebrate species for which large-scale genetic screens have been performed and extensively analyzed. Zebrafish mutations faithfully phenocopy many human disorders. Each mutation, once cloned, provides candidate genes and pathways for evaluation in the human. The collection of mutations in their entirety potentially provides a medical taxonomy, one based in developmental biology and genetics.
引用
收藏
页码:311 / 340
页数:34
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