ATF4 regulates SREBP1c expression to control in 3T3-L1 adipocytes differentiation fatty acids synthesis

被引:24
|
作者
Chen, Hu [1 ]
Yuan, Renqiang [1 ]
Zhang, Ying [1 ]
Zhang, Xumeng [1 ]
Chen, Luxi [1 ]
Zhou, Xingyu [1 ]
Yuan, Zhuning [1 ]
Nie, Yaping [1 ]
Li, Ming [1 ]
Mo, Delin [1 ]
Chen, Yaosheng [1 ]
机构
[1] Sun Yat Sen Univ, Sch Life Sci, State Key Lab Biocontrol, Guangzhou, Guangdong, Peoples R China
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS | 2016年 / 1859卷 / 11期
基金
中国国家自然科学基金;
关键词
ATF4; USP7; TRB3; SREBP1c; Transcription; PTM; ELEMENT-BINDING PROTEINS; ACTIVATED-RECEPTOR-GAMMA; TRANSCRIPTION FACTOR ATF4; PROTEASOME PATHWAY; LIPID-METABOLISM; PPAR-GAMMA; INSULIN; STRESS; LIVER; GENE;
D O I
10.1016/j.bbagrm.2016.07.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Activating transcription factor 4 (ATF4), which is highly expressed in 313-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. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:1459 / 1469
页数:11
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