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FOXO transcription factor stimulates repair

Jonathan B Weitzman

Genome Biology 2002, 3:spotlight-20020422-02  doi:10.1186/gb-spotlight-20020422-02

The electronic version of this article is the complete one and can be found online at:

Published:22 April 2002

© 2002 BioMed Central Ltd

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The protein kinase Akt promotes cell survival by phosphorylating and inhibiting FOXO forkhead transcription factors. FOXO factors have been linked to stress responses and the regulation of longevity. In the April 19 Science, Hien Tran and colleagues at Boston's Children's Hospital define a role for the FOXO3a family member in the response to DNA damage (Science 2002, 296:530-534). They created a Rat-1 fibroblast cell line expressing a tamoxifen-inducible FOXO3a protein. FOXO3a expression resulted in a delay in G2-M phase of the cell-cycle and enhanced DNA repair. Tran et al. performed a microarray screen to find FOXO3a-regulated genes and identified a number of genes involved in apoptosis and cell cycle regulation. They report that FOXO3a directly regulates transcription of the GADD45A gene upon damage of cellular DNA, and the ability of FOXO3a to induce DNA repair was reduced in cells lacking GADD45A. The role of FOXO3a in DNA repair, cell-cycle regulation and apoptosis probably contributes to its effect on organism life span.


  1. Akt promotes cell survival by phosphorylating and inhibiting a Forkhead transcription factor.

    PubMed Abstract | Publisher Full Text OpenURL

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    Children's Hospital Boston

  4. AFX-like Forkhead transcription factors mediate cell-cycle regulation by Ras and PKB through p27kip1.

    PubMed Abstract | Publisher Full Text OpenURL