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Fat specific protein 27 inhibits lipolysis by facilitating the inhibitory effect of Egr1 on transcription of adipose triglyceride lipase.


Singh M, Kaur R, Lee MJ, Pickering RT, Sharma VM, Puri V, Kandror KV

Lipolysis in fat tissue represents a major source of circulating fatty acids. Previously, we have found that lipolysis in adipocytes is controlled by early growth response transcription factor Egr1 that directly inhibits transcription of adipose triglyceride lipase, ATGL (Chakrabarti et al., Mol. Cell Biol. 2013, 33, 3659-3666). Here we demonstrate that knock down of the lipid droplet protein FSP27 (a.k.a. CIDEC) in human adipocytes increases expression of ATGL at the level of transcription, whereas over-expression of FSP27 has the opposite effect. FSP27 suppresses the activity of the ATGL promoter in vitro, and the proximal Egr1 binding site is responsible for this effect. FSP27 co-immunoprecipitates with Egr1 and increases its association with and inhibition of the ATGL promoter. Knockdown of Egr1 attenuates the inhibitory effect of FSP27. These results provide a new model of transcriptional regulation of ATGL.

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Bioruptor
Chromatin Shearing
ChIP-qPCR

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Published
May, 2014

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  • EpiChrom
    Umea Sweden
    Feb 27-Feb 28, 2020
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