Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8645486 | Gene | 2018 | 9 Pages |
Abstract
Fork head box O (FOXO) transcription factor is a key player in an evolutionarily conserved pathway. The mammalian FOXO family consists of FOXO1, 3, 4 and 6, are highly similar in their structure, function and regulation. To maintain optimum body function, the organisms have developed complex mechanisms for homeostasis. Importantly, it is well known that when these mechanisms dysregulate it results in the development of age-related disease. FOXO proteins are involved in a diverse cellular function and also have clinical significance including cell cycle arrest, cell differentiation, tumour suppression, DNA repair, longevity, diabetic complications, immunity, wound healing, regulation of metabolism and thus treatment of several types of diseases. By the combinations of post-translational modifications FOXO's serve as a 'molecular code' to sense external stimuli and recruit it as to specific regions of the genome and provide an integrated cellular response to changing physiological conditions. Akt/Protein kinase B a signaling pathway as a main regulator of FOXO to perform a diverse function in organisms. The present review summarizes the molecular and clinical aspects of FOXO transcription factor. And also elaborate the interaction of FOXO with the nucleosome remodelling complex to target genes, which is essential to cellular homeostasis.
Keywords
TLRPDHRTKAGEsIREDAF-16TGF-BMnSODARDSSwitch/sucrose non-fermentableCBPSir2CCR7MST1HSF1Gadd45NLSJnkCDKPI3KMMPFKHRHER2nESLPSFKHRL1PRMT1Skp2DBDMuRF1AFXc-Jun N-terminal kinaseERKsMAPKMdm2ROSSGKSWI/SNFAktAge-related diseasesTransforming Growth Factor Betatoll like receptorNuclear export sequencetumour necrosis factor-alphaforkhead Box Oforkhead boxDNA-Binding Domainnuclear localization sequenceAgingmanganese superoxide dismutaseFas LigandTNF-αFoxOTRAILTNF-related apoptosis-inducing ligandcalorie restrictionAdvanced glycation end-productHistone acetyl transferasesCREB binding proteinmitogen-activated protein kinasepyruvate dehydrogenasePtenHATscyclin dependent kinaseReactive oxygen speciesReceptor Tyrosine KinaseChemokine receptorsglucocorticoid receptor
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Authors
Neelam Tia, Alok Kumar Singh, Poorti Pandey, Chandra Shekhar Azad, Pritee Chaudhary, Indrajeet Singh Gambhir,