Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.
Sci. STKE, 4 March 2003
Vol. 2003, Issue 172, p. re5
[DOI: 10.1126/stke.2003.172.re5]
REVIEWS
The Many Forks in FOXO's Road
Hien Tran,
Anne Brunet,
Eric C. Griffith, and
Michael E. Greenberg*
Department of Neurobiology, Division of Neuroscience, Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Gloss: Many biological processes require the expression of new genes. A cell's ability to express new genes is controlled by proteins called transcription factors. One such family of transcription factors is the winged helix or Forkhead family of transcriptional regulators, of which the FOXO transcription factors are a subgroup. The FOXO subfamily of transcription factors can control various biological processes, including glucose metabolism, stress response, cell cycle regulation, and cell death, by regulating gene expression. At the organismal level, the regulation of gene expression by FOXO transcription factors is believed to play a role in pathological processes ranging from cancer and diabetes to organismal aging. A number of studies have shed light on how the FOXO transcription factors themselves are regulated and have also identified the gene targets controlled by FOXO transcription factors.
Nancy R. Gough, Lisa D. Chong, Elizabeth M. Adler, and L. Bryan Ray (4 March 2003) Sci. STKE2003 (172), eg4.
[DOI: 10.1126/stke.2003.172.eg4] |Full Text »|PDF »
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
O-GlcNAc Regulates FoxO Activation in Response to Glucose.
M. P. Housley, J. T. Rodgers, N. D. Udeshi, T. J. Kelly, J. Shabanowitz, D. F. Hunt, P. Puigserver, and G. W. Hart (2008)
J. Biol. Chem.
283, 16283-16292
|Abstract »|Full Text »|PDF »
EPO receptor circuits for primary erythroblast survival.
P. Sathyanarayana, A. Dev, J. Fang, E. Houde, O. Bogacheva, O. Bogachev, M. Menon, S. Browne, A. Pradeep, C. Emerson, et al. (2008)
Blood
111, 5390-5399
|Abstract »|Full Text »|PDF »
B Cell Receptor Signaling Down-Regulates Forkhead Box Transcription Factor Class O 1 mRNA Expression via Phosphatidylinositol 3-Kinase and Bruton's Tyrosine Kinase.
R. M. Hinman, J. N. Bushanam, W. A. Nichols, and A. B. Satterthwaite (2007)
J. Immunol.
178, 740-747
|Abstract »|Full Text »|PDF »
Akt-dependent Expression of NAIP-1 Protects Neurons against Amyloid-{beta} Toxicity.
S. Lesne, C. Gabriel, D. A. Nelson, E. White, E. T. MacKenzie, D. Vivien, and A. Buisson (2005)
J. Biol. Chem.
280, 24941-24947
|Abstract »|Full Text »|PDF »
Molecular and Cellular Determinants of Skeletal Muscle Atrophy and Hypertrophy.
Identification of Transcription Factor Binding Sites Upstream of Human Genes Regulated by the Phosphatidylinositol 3-Kinase and MEK/ERK Signaling Pathways.
J. W. Tullai, M. E. Schaffer, S. Mullenbrock, S. Kasif, and G. M. Cooper (2004)
J. Biol. Chem.
279, 20167-20177
|Abstract »|Full Text »|PDF »