Faculty Opinions recommendation of The longevity SNP rs2802292 uncovered: HSF1 activates stress-dependent expression of FOXO3 through an intronic enhancer.
Year: 2018
Type: peer-review
Abstract: The HSF and FOXO families of transcription factors play evolutionarily conserved roles in stress resistance and lifespan.In humans, the rs2802292 G-allele at FOXO3 locus has been associated with longevity in all human populations tested; moreover, its copy number correlated with reduced frequency of age-related diseases in centenarians.At the molecular level, the intronic rs2802292 G-allele correlated with increased expression of FOXO3, suggesting that FOXO3 intron 2 may represent a regulatory region.Here we show that the 90-bp sequence around the intronic single nucleotide polymorphism rs2802292 has enhancer functions, and that the rs2802292 G-allele creates a novel HSE binding site for HSF1, which induces FOXO3 expression in response to diverse stress stimuli.At the molecular level, HSF1 mediates the occurrence of a promoter-enhancer interaction at FOXO3 locus involving the 5 UTR and the rs2802292 region.These data were confirmed in various cellular models including human HAP1 isogenic cell lines (G/T).Our functional studies highlighted the importance of the HSF1-FOXO3-SOD2/CAT/GADD45A cascade in cellular stress response and survival by promoting ROS detoxification, redox balance and DNA repair.Our findings suggest the existence of an HSF1-FOXO3 axis in human cells that could be involved in stress response pathways functionally regulating lifespan and disease susceptibility.
Author: Aaron Russell
Institution: Deakin University
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: green
Awards: G3963606767, G6067122168, G6890540292
OpenAlex ID: W4234987244