| Literature DB >> 27452504 |
Hu Chen1, Renqiang Yuan1, Ying Zhang1, Xumeng Zhang1, Luxi Chen1, Xingyu Zhou1, Zhuning Yuan1, Yaping Nie1, Ming Li1, Delin Mo2, Yaosheng Chen3.
Abstract
Activating transcription factor 4 (ATF4), which is highly expressed in 3T3-L1 adipocytes after adipogenic induction, is essential for adipocytes differentiation. ATF4 also plays a vital role in regulating fatty acids biosynthesis, whereas the detailed mechanism of this process is still unclear. Here we demonstrated that siRNA-based ATF4 depletion in 3T3-L1 adipocytes significantly reduced the accumulation of fatty acids and triglycerides. Moreover, SREBP1c protein, which is an important transcription factor of lipogenesis, appreciably decreased while Srebp1c mRNA increased. Then we identified that ATF4 could maintain SREBP1c protein stability by directly activating the expression of USP7 which deubiquitinates SREBP1c and increases its protein content in cell. Besides, USP7 could restore the synthesis of fatty acids and triglycerides in the absence of ATF4. On the other hand, we found that ATF4 might inhibit the transcription of Srebp1c through TRB3, which is repressed by IBMX and DEX during early adipogenesis. Thus, our data indicate that ATF4 regulates SREBP1c expression to control fatty acids synthesis.Entities:
Keywords: ATF4; PTM; SREBP1c; TRB3; Transcription; USP7
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Year: 2016 PMID: 27452504 DOI: 10.1016/j.bbagrm.2016.07.010
Source DB: PubMed Journal: Biochim Biophys Acta ISSN: 0006-3002