Department of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, United States.
Department of Molecular Biology and Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, United States.
Elife. 2018 Jun 27;7:e36826. doi: 10.7554/eLife.36826.
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, LXRα and C/EBPβ, 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/EBPβ and LXRα 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.
在肥胖症中,升高的胰岛素通过激活编码 SREBP-1c 的基因使脂肪肝,SREBP-1c 是一种增强脂肪酸合成的转录因子。两种转录因子,LXRα 和 C/EBPβ,对于胰岛素诱导肝脏 SREBP-1c mRNA 是必需但不充分的。在这里,我们表明第三个转录因子 BHLHE40 也是必需的。免疫沉淀显示,BHLHE40 在禁食后再喂食的大鼠肝脏中与 C/EBPβ 和 LXRα 结合。当禁食大鼠再喂食时,或当大鼠肝细胞用胰岛素孵育时,肝 BHLHE40 mRNA 迅速升高。通过在小鼠中基因敲除或在肝细胞中使用 siRNA 来阻止这种升高,可降低胰岛素诱导的 SREBP-1c mRNA 升高。尽管 BHLHE40 对于胰岛素诱导的 SREBP-1c 是必需的,但正如在没有胰岛素的情况下,慢病毒 BHLHE40 过表达未能增加肝细胞 SREBP-1c mRNA 所证明的那样,它并不充分。因此,胰岛素增加 SREBP-1c mRNA 需要额外的事件。