Epigenetic regulation of Cebpb activation by pY19-Caveolin-2 at the nuclear periphery in association with the nuclear lamina
- Authors
- Choi, Moonjeong; Kwon, Hayeong; Jeong, Kyuho; Pak, Yunbae
- Issue Date
- Dec-2022
- Publisher
- Elsevier BV
- Keywords
- Caveolin-2; Cebpb; Lamin A; C; Lamin B1; Epigenetic activation; KDM4b
- Citation
- Biochimica et Biophysica Acta - Molecular Cell Research, v.1869, no.12
- Indexed
- SCIE
SCOPUS
- Journal Title
- Biochimica et Biophysica Acta - Molecular Cell Research
- Volume
- 1869
- Number
- 12
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/29367
- DOI
- 10.1016/j.bbamcr.2022.119363
- ISSN
- 0167-4889
1879-2596
- Abstract
- Here, we show that Caveolin-2 (Cav-2) is an epigenetic regulator for adipogenesis. Upon adipogenic stimulation, inner nuclear membrane (INM)-targeted pY19-Cav-2 interacted with lamin A/C to disengage the repressed Cebpb promoter from lamin A/C, which facilitated the Cebpb promoter association with lamin B1. Consequently, pY19-Cav-2 recruited lysine demethylase 4b (KDM4b) for demethylation of histone H3 lysine 9 trimethylation (H3K9me3) and histone acetyltransferase GCN5 for acetylation of H3K27, and subsequently RNA polymerase II (Pol II) on Cebpb promoter for epigenetic activation of Cebpb, to initiate adipogenesis. Cav-2 knock-down abrogated the Cebpb activation and blocked the Pparg2 and Cebpa activation. Re-expression of Cav-2 restored Cebpb activation and adipogenesis in Cav-2-deficient preadipocytes. Our data identify a new mechanism by which the epigenetic activation of Cebpb is controlled at the nuclear periphery to promote adipogenesis.
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