TY - JOUR
T1 - VDR gene methylation as a molecular adaption to light exposure
T2 - Historic, recent and genetic influences
AU - Beckett, Emma L.
AU - Jones, Patrice
AU - Veysey, Martin
AU - Duesing, Konsta
AU - Martin, Charlotte
AU - Furst, John
AU - Yates, Zoe
AU - Jablonski, Nina G.
AU - Chaplin, George
AU - Lucock, Mark
N1 - Publisher Copyright:
© 2017 Wiley Periodicals, Inc.
PY - 2017/9/1
Y1 - 2017/9/1
N2 - Objectives: The vitamin D receptor (VDR) is a member of the nuclear receptor family of transcription factors. We examined whether degree of VDR gene methylation acts as a molecular adaptation to light exposure. We explored this in the context of photoperiod at conception, recent UV irradiance at 305 nm, and gene-latitude effects. METHODS: Eighty subjects were examined for VDR gene-CpG island methylation density. VDR gene variants were also examined by PCR-RFLP. RESULTS: Photoperiod at conception was significantly positively related to VDR methylation density, explaining 17% of the variance in methylation (r2= 0.17; P =.001). Within this model, photoperiod at conception and plasma 25(OH)D independently predicted methylation density at the VDR-CpG island. Recent UV exposure at 305 nm led to a fivefold increase in mean methylation density (P =.02). Again, UV exposure and plasma 25(OH)D independently predicted methylation density at the VDR-CpG island. In the presence of the BsmI mutant allele, methylation density was increased (P =.01), and in the presence of the TaqI or FokI mutant allele, methylation density was decreased (P =.007 and.04 respectively). Multivariate modelling suggests plasma 25(OH)D, photoperiod at conception, recent solar irradiance, and VDR genotype combine as independent predictors of methylation at the VDR-CpG island, explaining 34% of the variance in methylation (R2= 0.34, P <.0001). CONCLUSIONS: Duration of early-life light exposure and strength of recent irradiance, along with latitudinal genetic factors, influence degree of VDR gene methylation consistent with this epigenetic phenomenon being a molecular adaptation to variation in ambient light exposure. Findings contribute to our understanding of human biology.
AB - Objectives: The vitamin D receptor (VDR) is a member of the nuclear receptor family of transcription factors. We examined whether degree of VDR gene methylation acts as a molecular adaptation to light exposure. We explored this in the context of photoperiod at conception, recent UV irradiance at 305 nm, and gene-latitude effects. METHODS: Eighty subjects were examined for VDR gene-CpG island methylation density. VDR gene variants were also examined by PCR-RFLP. RESULTS: Photoperiod at conception was significantly positively related to VDR methylation density, explaining 17% of the variance in methylation (r2= 0.17; P =.001). Within this model, photoperiod at conception and plasma 25(OH)D independently predicted methylation density at the VDR-CpG island. Recent UV exposure at 305 nm led to a fivefold increase in mean methylation density (P =.02). Again, UV exposure and plasma 25(OH)D independently predicted methylation density at the VDR-CpG island. In the presence of the BsmI mutant allele, methylation density was increased (P =.01), and in the presence of the TaqI or FokI mutant allele, methylation density was decreased (P =.007 and.04 respectively). Multivariate modelling suggests plasma 25(OH)D, photoperiod at conception, recent solar irradiance, and VDR genotype combine as independent predictors of methylation at the VDR-CpG island, explaining 34% of the variance in methylation (R2= 0.34, P <.0001). CONCLUSIONS: Duration of early-life light exposure and strength of recent irradiance, along with latitudinal genetic factors, influence degree of VDR gene methylation consistent with this epigenetic phenomenon being a molecular adaptation to variation in ambient light exposure. Findings contribute to our understanding of human biology.
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U2 - 10.1002/ajhb.23010
DO - 10.1002/ajhb.23010
M3 - Article
C2 - 28432711
AN - SCOPUS:85018641385
SN - 1042-0533
VL - 29
JO - American Journal of Human Biology
JF - American Journal of Human Biology
IS - 5
M1 - e23010
ER -