Investigation of changes in DNA methylation associated with alterations in gene expression resulting in differences between lean and obese adipogenesis
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Lim, Jiwon
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Heo, Yerim
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Kangwon Natl Univ, Inst Biosci & Biotechnol, Coll Biomed Sci, Div Biomed Convergence, Chunchon 24341, South KoreaKangwon Natl Univ, Inst Biosci & Biotechnol, Coll Biomed Sci, Div Biomed Convergence, Chunchon 24341, South Korea
Heo, Yerim
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Choi, Sun Shim
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Kangwon Natl Univ, Inst Biosci & Biotechnol, Coll Biomed Sci, Div Biomed Convergence, Chunchon 24341, South KoreaKangwon Natl Univ, Inst Biosci & Biotechnol, Coll Biomed Sci, Div Biomed Convergence, Chunchon 24341, South Korea
Choi, Sun Shim
[1
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[1] Kangwon Natl Univ, Inst Biosci & Biotechnol, Coll Biomed Sci, Div Biomed Convergence, Chunchon 24341, South Korea
DNA methylation (DNAm) is an important epigenetic regulator controlling various cellular activities, including cell proliferation and differentiation. In the present work, we examined alterations in DNAm associated with obesity using methylome and transcriptome data from 27 purified adipocytes (ACs) and 7 preadipocytes (preACs) in human visceral adipose tissue (VAT) samples. We identified differentially methylated probes (DMPs) using two methods: (i) DMPs that were obtained from a comparison of the DNAm levels between AC and preAC samples (AGDMPs) and (ii) DMPs that were obtained from a comparison of the DNAm levels between obese and lean AC samples (ACDMPs). These two classes of DMPs were obtained to identify a relationship between adipogenesis and obesity. We also investigated how hyper and hypomethylation of the promoter and/or gene body differentially affected changes in gene expression by estimating the odds ratios (ORs) of changes in gene expression without DMPs in the background. Interestingly, the magnitude of DNAm alterations during AC differentiation was greater under lean conditions than under obese conditions. In conclusion, several adipogenesisrelated genes were affected by complicated methylation changes and ultimately cause differences in gene expression in ACs under lean and obese conditions.
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Univ So Calif, Dept Biochem & Mol Biol, Keck Sch Med, Los Angeles, CA 90089 USA
Univ Calif Davis, Genet Grad Grp, Davis, CA 95676 USAUniv So Calif, Dept Biochem & Mol Biol, Keck Sch Med, Los Angeles, CA 90089 USA
Blattler, Adam
Farnham, Peggy J.
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Univ So Calif, Dept Biochem & Mol Biol, Keck Sch Med, Los Angeles, CA 90089 USAUniv So Calif, Dept Biochem & Mol Biol, Keck Sch Med, Los Angeles, CA 90089 USA
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Louisiana State Univ Syst, Pennington Biomed Res Ctr, Baton Rouge, LA 70803 USALouisiana State Univ Syst, Pennington Biomed Res Ctr, Baton Rouge, LA 70803 USA
de Sa, Paula Mota
Richard, Allison J.
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Louisiana State Univ Syst, Pennington Biomed Res Ctr, Baton Rouge, LA 70803 USALouisiana State Univ Syst, Pennington Biomed Res Ctr, Baton Rouge, LA 70803 USA
Richard, Allison J.
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Hang, Hardy
Stephens, Jacqueline M.
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Louisiana State Univ Syst, Pennington Biomed Res Ctr, Baton Rouge, LA 70803 USALouisiana State Univ Syst, Pennington Biomed Res Ctr, Baton Rouge, LA 70803 USA
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Univ So Calif, Dept Biochem & Mol Biol, Keck Sch Med, Los Angeles, CA 90089 USA
Univ Calif Davis, Genet Grad Grp, Davis, CA 95676 USAUniv So Calif, Dept Biochem & Mol Biol, Keck Sch Med, Los Angeles, CA 90089 USA
Blattler, Adam
Farnham, Peggy J.
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Univ So Calif, Dept Biochem & Mol Biol, Keck Sch Med, Los Angeles, CA 90089 USAUniv So Calif, Dept Biochem & Mol Biol, Keck Sch Med, Los Angeles, CA 90089 USA
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Louisiana State Univ Syst, Pennington Biomed Res Ctr, Baton Rouge, LA 70803 USALouisiana State Univ Syst, Pennington Biomed Res Ctr, Baton Rouge, LA 70803 USA
de Sa, Paula Mota
Richard, Allison J.
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Louisiana State Univ Syst, Pennington Biomed Res Ctr, Baton Rouge, LA 70803 USALouisiana State Univ Syst, Pennington Biomed Res Ctr, Baton Rouge, LA 70803 USA
Richard, Allison J.
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Hang, Hardy
Stephens, Jacqueline M.
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Louisiana State Univ Syst, Pennington Biomed Res Ctr, Baton Rouge, LA 70803 USALouisiana State Univ Syst, Pennington Biomed Res Ctr, Baton Rouge, LA 70803 USA