PUBLICATION

From zebrafish to human: modular medical models

Authors
Shin, J.T. and Fishman, M.C.
ID
ZDB-PUB-020807-24
Date
2002
Source
Annual review of genomics and human genetics   3: 311-340 (Review)
Registered Authors
Fishman, Mark C., Shin, Jordan
Keywords
none
MeSH Terms
  • Animals
  • Disease Models, Animal*
  • Genetic Diseases, Inborn/genetics*
  • Genetics, Medical*
  • Genome*
  • Genome, Human*
  • Humans
  • Models, Genetic
  • Mutation
  • Phenotype
  • Zebrafish/genetics*
PubMed
12142362 Full text @ Annu. Rev. Genomics Hum. Genet.
Abstract
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.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping