Novel DNA Methylation Sites Influence GPR15 Expression in Relation to Smoking
Smoking is a major risk factor for cardiovascular diseases and has been implicated in the regulation of the G protein-coupled receptor 15 (GPR15) by affecting CpG methylation. The G protein-coupled receptor 15 is involved in angiogenesis and inflammation. An effect on gene regulation has been shown...
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Veröffentlicht in: | Biomolecules (Basel, Switzerland) Switzerland), 2018-08, Vol.8 (3), p.74 |
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Zusammenfassung: | Smoking is a major risk factor for cardiovascular diseases and has been implicated in the regulation of the G protein-coupled receptor 15 (GPR15) by affecting CpG methylation. The G protein-coupled receptor 15 is involved in angiogenesis and inflammation. An effect on
gene regulation has been shown for the CpG site CpG3.98251294. We aimed to analyze the effect of smoking on
expression and methylation sites spanning the
locus. DNA methylation of nine
CpG sites was measured in leukocytes from 1291 population-based individuals using the EpiTYPER. Monocytic
expression was measured by qPCR at baseline and five-years follow up.
gene expression was upregulated in smokers (beta (ß) = -2.699,
-value (
) = 1.02 × 10
) and strongly correlated with smoking exposure (ß = -0.063,
= 2.95 × 10
). Smoking cessation within five years reduced
expression about 19% (
= 9.65 × 10
) with decreasing
expression over time (ß = 0.031,
= 3.81 × 10
). Additionally, three novel CpG sites within
affected by smoking were identified. For CpG3.98251047, DNA methylation increased steadily after smoking cessation (ß = 0.123,
= 1.67 × 10
) and strongly correlated with changes in
expression (ß = 0.036,
= 4.86 × 10
). Three novel
CpG sites were identified in relation to smoking and
expression. Our results provide novel insights in the regulation of GPR15, which possibly linked smoking to inflammation and disease progression. |
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ISSN: | 2218-273X 2218-273X |
DOI: | 10.3390/biom8030074 |