Literature search services are currently unavailable. During our hosting provider's UPS upgrade we experienced a hardware failure and are currently working to resolve the issue.

Preparing your results

Our searching services are busy right now. Your search will reload in five seconds.

Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

Disruption of forkhead transcription factor (FOXO) family members in mice reveals their functional diversification.

Genetic analysis in Caenorhabditis elegans has uncovered essential roles for DAF-16 in longevity, metabolism, and reproduction. The mammalian orthologs of DAF-16, the closely-related FOXO subclass of forkhead transcription factors (FKHR/FOXO1, FKHRL1/FOXO3a, and AFX/FOXO4), also have important roles in cell cycle arrest, apoptosis and stress responses in vitro, but their in vivo physiological roles are largely unknown. To elucidate their role in normal development and physiology, we disrupted each of the Foxo genes in mice. Foxo1-null embryos died on embryonic day 10.5 as a consequence of incomplete vascular development. Foxo1-null embryonic and yolk sac vessels were not well developed at embryonic day 9.5, and Foxo1 expression was found in a variety of embryonic vessels, suggesting a crucial role of this transcription factor in vascular formation. On the other hand, both Foxo3a- and Foxo4-null mice were viable and grossly indistinguishable from their littermate controls, indicating dispensability of these two members of the Foxo transcription factor family for normal vascular development. Foxo3a-null females showed age-dependent infertility and had abnormal ovarian follicular development. In contrast, histological analyses of Foxo4-null mice did not identify any consistent abnormalities. These results demonstrate that the physiological roles of Foxo genes are functionally diverse in mammals.

Pubmed ID: 14978268


  • Hosaka T
  • Biggs WH
  • Tieu D
  • Boyer AD
  • Varki NM
  • Cavenee WK
  • Arden KC


Proceedings of the National Academy of Sciences of the United States of America

Publication Data

March 2, 2004

Associated Grants

  • Agency: NCI NIH HHS, Id: CA68672

Mesh Terms

  • Animals
  • Embryonic and Fetal Development
  • Female
  • Fetal Death
  • Forkhead Transcription Factors
  • Gene Expression Regulation, Developmental
  • Genetic Variation
  • Infertility, Female
  • Male
  • Mice
  • Multigene Family
  • Neovascularization, Physiologic
  • Ovary
  • Sequence Deletion
  • Transcription Factors
  • Yolk Sac