Background: Obesity is a major worldwide threat to human health. Increasing evidence indicates that epigenetic modifications have a major impact on the natural history of this disorder. Ankyrin Repeat Domain 26 (Ankrd26) is involved in the development of both obesity and diabetes in mice and is modulated by environmentally induced epigenetic modifications. This study aims at investigating whether impaired ANKRD26 gene expression and methylation occur in human obesity and whether they correlate to the phenotype of these subjects. Results: We found that downregulation of ANKRD26 mRNA and hyper-methylation of a specific region of the ANKRD26 promoter, embedding the CpG dinucleotides - 689, - 659, and - 651 bp, occur in peripheral blood leukocytes from obese compared with the lean subjects. ANKRD26 gene expression correlates inversely to the percentage of DNA methylation at these 3 CpG sites. Luciferase assays reveal a cause-effect relationship between DNA methylation at the 3 CpG sites and ANKRD26 gene expression. Finally, both ANKRD26 mRNA levels and CpG methylation correlate to body mass index and to the pro-inflammatory status and the increased cardio-metabolic risk factors of these same subjects. Conclusion: Downregulation of the ANKRD26 gene and hyper-methylation at specific CpGs of its promoter are common abnormalities in obese patients. These changes correlate to the pro-inflammatory profile and the cardio-metabolic risk factors of the obese individuals, indicating that, in humans, they mark adverse health outcomes. © 2019 The Author(s).

Epigenetic silencing of the ANKRD26 gene correlates to the pro-inflammatory profile and increased cardio-metabolic risk factors in human obesity / Desiderio, A.; Longo, M.; Parrillo, L.; Campitelli, M.; Cacace, G.; De Simone, S.; Spinelli, R.; Zatterale, F.; Cabaro, S.; Dolce, P.; Formisano, P.; Milone, M.; Miele, C.; Beguinot, F.; Raciti, G. A.. - In: CLINICAL EPIGENETICS. - ISSN 1868-7083. - 11:1(2019), p. 181. [10.1186/s13148-019-0768-0]

Epigenetic silencing of the ANKRD26 gene correlates to the pro-inflammatory profile and increased cardio-metabolic risk factors in human obesity

Desiderio A.;Longo M.;Parrillo L.;Campitelli M.;Spinelli R.;Zatterale F.;Cabaro S.;Dolce P.;Formisano P.;Milone M.;Beguinot F.;Raciti G. A.
2019

Abstract

Background: Obesity is a major worldwide threat to human health. Increasing evidence indicates that epigenetic modifications have a major impact on the natural history of this disorder. Ankyrin Repeat Domain 26 (Ankrd26) is involved in the development of both obesity and diabetes in mice and is modulated by environmentally induced epigenetic modifications. This study aims at investigating whether impaired ANKRD26 gene expression and methylation occur in human obesity and whether they correlate to the phenotype of these subjects. Results: We found that downregulation of ANKRD26 mRNA and hyper-methylation of a specific region of the ANKRD26 promoter, embedding the CpG dinucleotides - 689, - 659, and - 651 bp, occur in peripheral blood leukocytes from obese compared with the lean subjects. ANKRD26 gene expression correlates inversely to the percentage of DNA methylation at these 3 CpG sites. Luciferase assays reveal a cause-effect relationship between DNA methylation at the 3 CpG sites and ANKRD26 gene expression. Finally, both ANKRD26 mRNA levels and CpG methylation correlate to body mass index and to the pro-inflammatory status and the increased cardio-metabolic risk factors of these same subjects. Conclusion: Downregulation of the ANKRD26 gene and hyper-methylation at specific CpGs of its promoter are common abnormalities in obese patients. These changes correlate to the pro-inflammatory profile and the cardio-metabolic risk factors of the obese individuals, indicating that, in humans, they mark adverse health outcomes. © 2019 The Author(s).
2019
Epigenetic silencing of the ANKRD26 gene correlates to the pro-inflammatory profile and increased cardio-metabolic risk factors in human obesity / Desiderio, A.; Longo, M.; Parrillo, L.; Campitelli, M.; Cacace, G.; De Simone, S.; Spinelli, R.; Zatterale, F.; Cabaro, S.; Dolce, P.; Formisano, P.; Milone, M.; Miele, C.; Beguinot, F.; Raciti, G. A.. - In: CLINICAL EPIGENETICS. - ISSN 1868-7083. - 11:1(2019), p. 181. [10.1186/s13148-019-0768-0]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/788956
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