Literature DB >> 18391970

The FoxO code.

D R Calnan1, A Brunet.   

Abstract

The FoxO family of Forkhead transcription factors plays an important role in longevity and tumor suppression by upregulating target genes involved in stress resistance, metabolism, cell cycle arrest and apoptosis. FoxO transcription factors translate a variety of environmental stimuli, including insulin, growth factors, nutrients and oxidative stress, into specific gene-expression programs. These environmental stimuli control FoxO activity primarily by regulating their subcellular localization, but also by affecting their protein levels, DNA-binding properties and transcriptional activity. The precise regulation of FoxO transcription factors is enacted by an intricate combination of post-translational modifications (PTMs), including phosphorylation, acetylation and ubiquitination, and binding protein partners. An intriguing possibility is that FoxO PTMs may act as a 'molecular FoxO code' read by selective protein partners to rapidly regulate gene-expression programs. The effective control of FoxO activity in response to environmental stimuli is likely to be critical to prevent aging and age-dependent diseases, including cancer, neurodegenerative diseases and diabetes.

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Year:  2008        PMID: 18391970     DOI: 10.1038/onc.2008.21

Source DB:  PubMed          Journal:  Oncogene        ISSN: 0950-9232            Impact factor:   9.867


  544 in total

1.  Lysine methylation of FOXO3 regulates oxidative stress-induced neuronal cell death.

Authors:  Qi Xie; Yumin Hao; Li Tao; Shengyi Peng; Chitong Rao; Hong Chen; Han You; Meng-qiu Dong; Zengqiang Yuan
Journal:  EMBO Rep       Date:  2012-04       Impact factor: 8.807

2.  The role of E2F-1 and downstream target genes in mediating ischemia/reperfusion injury in vivo.

Authors:  Ekaterini Angelis; Peng Zhao; Rui Zhang; Joshua I Goldhaber; W Robb Maclellan
Journal:  J Mol Cell Cardiol       Date:  2011-09-22       Impact factor: 5.000

Review 3.  Highly specialized role of Forkhead box O transcription factors in the immune system.

Authors:  Anne S Dejean; Stephen M Hedrick; Yann M Kerdiles
Journal:  Antioxid Redox Signal       Date:  2010-12-13       Impact factor: 8.401

4.  miR-451 protects against erythroid oxidant stress by repressing 14-3-3zeta.

Authors:  Duonan Yu; Camila O dos Santos; Guowei Zhao; Jing Jiang; Julio D Amigo; Eugene Khandros; Louis C Dore; Yu Yao; Janine D'Souza; Zhe Zhang; Saghi Ghaffari; John Choi; Sherree Friend; Wei Tong; Jordan S Orange; Barry H Paw; Mitchell J Weiss
Journal:  Genes Dev       Date:  2010-08-01       Impact factor: 11.361

Review 5.  New insights for FOXO and cell-fate decision in HIV infection and HIV associated neurocognitive disorder.

Authors:  Min Cui; Yunlong Huang; Yong Zhao; Jialin Zheng
Journal:  Adv Exp Med Biol       Date:  2009       Impact factor: 2.622

6.  Synaptic activity and nuclear calcium signaling protect hippocampal neurons from death signal-associated nuclear translocation of FoxO3a induced by extrasynaptic N-methyl-D-aspartate receptors.

Authors:  Oliver Dick; Hilmar Bading
Journal:  J Biol Chem       Date:  2010-04-19       Impact factor: 5.157

7.  mTORC1 activates SREBP-1c and uncouples lipogenesis from gluconeogenesis.

Authors:  Mathieu Laplante; David M Sabatini
Journal:  Proc Natl Acad Sci U S A       Date:  2010-02-18       Impact factor: 11.205

8.  FOXO transcription factors in non-alcoholic fatty liver disease.

Authors:  X Charlie Dong
Journal:  Liver Res       Date:  2017-09

9.  Impaired myogenesis in estrogen-related receptor γ (ERRγ)-deficient skeletal myocytes due to oxidative stress.

Authors:  Jennifer Murray; Johan Auwerx; Janice M Huss
Journal:  FASEB J       Date:  2012-10-04       Impact factor: 5.191

10.  SirT3 regulates the mitochondrial unfolded protein response.

Authors:  Luena Papa; Doris Germain
Journal:  Mol Cell Biol       Date:  2013-12-09       Impact factor: 4.272

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