Of flies and men--studying human disease in Drosophila

Curr Opin Genet Dev. 2001 Jun;11(3):274-8. doi: 10.1016/s0959-437x(00)00190-8.

Abstract

During the past year, the Drosophila genome has been sequenced. More than 60% of genes implicated in human disease have Drosophila orthologues. Developments in RNA-mediated interference and homologous recombination have made 'reverse genetics' feasible in Drosophila. Conventional Drosophila genetics is being used increasingly to place human disease genes of unknown function in the context of functional pathways.

Publication types

  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Animals
  • Disease
  • Drosophila melanogaster / genetics*
  • Genetic Predisposition to Disease / genetics*
  • Humans