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Updated: Jan 25, 2026
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Published on: February 9, 2022
Tet2-mediated Pref-1 activation delays adipocyte differentiation
Brigitta Veda Devani1, Hye Su Moon1, Ana Braza1
1Soonchunhyang Institute of Medi-Bio Science, Soonchunhyang University, Cheonan-si, Chungcheongnam-do, 31151, Republic of Korea; Department of Integrated Biomedical Science, Soonchunhyang University, Cheonan-si, Chungcheongnam-do, 31151, Republic of Korea.
None:
Ten-eleven translocation 2 (Tet2) catalyzes the conversion of 5-methylcytosine to 5-hydroxymethylcytosine, facilitating active DNA demethylation. Although implicated in adipogenesis, its precise role remains controversial. Here, we investigated Tet2 function during early 3T3-L1 adipocyte differentiation, focusing on regulation of the imprinted gene Pref-1. Differentiation time-course experiments revealed that Tet2 protein, but not mRNA, was progressively reduced via proteasome-dependent degradation, contrasting with previous reports of Tet2 mRNA upregulation. Tet2 overexpression delayed lipid accumulation and reduced adipogenic marker expression, whereas knockdown had the opposite effect. Mechanistically, Tet2 positively regulated Pref-1 transcription by demethylating specific differentially methylated regions in its promoter and exon 6. Loss of Tet2 increased DNA methylation and decreased hydroxymethylation at these loci, leading to Pref-1 repression and derepression of C/EBPα and PPARγ. This stage-specific, proteasome-mediated downregulation of Tet2 integrates epigenetic and post-translational control to regulate adipocyte commitment. The Tet2-Pref-1 axis offers mechanistic insight into adipose tissue expansion and may represent a therapeutic target for obesity and imprinting-related disorders.
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