BHLHE40, a third transcription factor required for insulin induction of SREBP-1c mRNA in rodent liver

被引:22
|
作者
Tian, Jing [1 ]
Wu, Jiaxi [2 ,3 ]
Chen, Xiang [2 ,3 ]
Guo, Tong [1 ]
Chen, Zhijian J. [2 ,3 ]
Goldstein, Joseph L. [1 ]
Brown, Michael S. [1 ]
机构
[1] Univ Texas Southwestern Med Ctr Dallas, Dept Mol Genet, Dallas, TX 75390 USA
[2] Univ Texas Southwestern Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA
[3] Univ Texas Southwestern Med Ctr Dallas, Howard Hughes Med Inst, Dallas, TX USA
来源
ELIFE | 2018年 / 7卷
基金
美国国家卫生研究院;
关键词
FATTY-ACID SYNTHESIS; X-RECEPTOR; GENE; STIMULATION; LIPOGENESIS; INHIBITION; RESISTANCE; PATHWAY; GLUCOSE; BETA;
D O I
10.7554/eLife.36826
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In obesity, elevated insulin causes fatty liver by activating the gene encoding SREBP-1c, a transcription factor that enhances fatty acid synthesis. Two transcription factors, LXR alpha and C/EBP beta, are necessary but not sufficient for insulin induction of hepatic SREBP-1c mRNA. Here, we show that a third transcription factor, BHLHE40, is required. Immunoprecipitation revealed that BHLHE40 binds to C/EBP beta and LXR alpha in livers of rats that had fasted and then refed. Hepatic BHLHE40 mRNA rises rapidly when fasted rats are refed and when rat hepatocytes are incubated with insulin. Preventing this rise by gene knockout in mice or siRNAs in hepatocytes reduces the insulin-induced rise in SREBP-1c mRNA. Although BHLHE40 is necessary for insulin induction of SREBP-1c, it is not sufficient as demonstrated by failure of lentiviral BHLHE40 overexpression to increase hepatocyte SREBP-1c mRNA in the absence of insulin. Thus, an additional event is required for insulin to increase SREBP-1c mRNA.
引用
收藏
页数:18
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