Cebpa gebe expression is stimulated by Pparg and Mll4,(Mll3) complex

Stable Identifier
R-MMU-9858204
Type
Reaction [omitted]
Species
Mus musculus
Compartment
ReviewStatus
3/5
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Cebpa gebe expression is stimulated by Pparg and Mll4,(Mll3) complex
In mouse embryonic fibroblasts (MEFs) in which Pparg was ectopically expressed, Pparg positively regulates Cebpa transcription in a ligand-dependent manner (Ge et a. 2008).

MEFs deficient for Paxip1 (Ptip), an accessory subunit of Kmt2c (Mll3) and Kmt2d (Mll4) complexes, show a severe defect in Pparg- and ligand-stimulated expression of endogenous Cebpa (Cho et al. 2009). In differentiating mouse brown preadipocytes, Paxip1 promotes recruitment of RNA Pol II to Cebpa gene promoter (Cho et al. 2009).

In mouse brown preadipocytes expressing histone 3 mutant H3.3 K4M, the expression of the Cebpa gene is severely reduced (Jang et al. 2019). Deletion of SET domains of Kmt2c and Kmt2d in mouse brown preadipocytes prevents induction of Cebpa during adipogenesis (Jang et al. 2019).
Literature References
PubMed ID Title Journal Year
30335158 H3.3K4M destabilizes enhancer H3K4 methyltransferases MLL3/MLL4 and impairs adipose tissue development

Park, YK, Lee, JE, Froimchuk, E, Jang, Y, Broun, A, Wang, C, Liu, C, Zhuang, L, Ge, K

Nucleic Acids Res 2019
18039840 Alternative mechanisms by which mediator subunit MED1/TRAP220 regulates peroxisome proliferator-activated receptor gamma-stimulated adipogenesis and target gene expression

Hong, TB, Guermah, M, Cho, YW, Ge, K, Kalkum, M, Yu, H, Ito, M, Roeder, RG, Guo, H

Mol Cell Biol 2008
19583951 Histone methylation regulator PTIP is required for PPARgamma and C/EBPalpha expression and adipogenesis

Ge, K, Wang, L, Hong, S, Gavrilova, O, Lee, JE, Jin, Q, Cho, YW

Cell Metab 2009
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