Dempersmier Jon, Sambeat Audrey, Gulyaeva Olga, Paul Sarah M, Hudak Carolyn S S, Raposo Helena F, Kwan Hiu-Yee, Kang Chulho, Wong Roger H F, Sul Hei Sook
Department of Nutritional Science & Toxicology, University of California, Berkeley, Berkeley, CA 94720, USA; Comparative Biochemistry Program, University of California, Berkeley, Berkeley, CA 94720, USA.
Department of Nutritional Science & Toxicology, University of California, Berkeley, Berkeley, CA 94720, USA.
Mol Cell. 2015 Jan 22;57(2):235-46. doi: 10.1016/j.molcel.2014.12.005. Epub 2015 Jan 8.
Uncoupling protein 1 (UCP1) mediates nonshivering thermogenesis and, upon cold exposure, is induced in brown adipose tissue (BAT) and subcutaneous white adipose tissue (iWAT). Here, by high-throughput screening using the UCP1 promoter, we identify Zfp516 as a transcriptional activator of UCP1 as well as PGC1α, thereby promoting a BAT program. Zfp516 itself is induced by cold and sympathetic stimulation through the cAMP-CREB/ATF2 pathway. Zfp516 directly binds to the proximal region of the UCP1 promoter, not to the enhancer region where other transcription factors bind, and interacts with PRDM16 to activate the UCP1 promoter. Although ablation of Zfp516 causes embryonic lethality, knockout embryos still show drastically reduced BAT mass. Overexpression of Zfp516 in adipose tissue promotes browning of iWAT even at room temperature, increasing body temperature and energy expenditure and preventing diet-induced obesity. Zfp516 may represent a future target for obesity therapeutics.
解偶联蛋白1(UCP1)介导非颤抖性产热,在冷暴露时,它在棕色脂肪组织(BAT)和皮下白色脂肪组织(iWAT)中被诱导表达。在此,通过使用UCP1启动子的高通量筛选,我们鉴定出Zfp516是UCP1以及PGC1α的转录激活因子,从而促进棕色脂肪组织程序。Zfp516自身通过cAMP-CREB/ATF2途径被寒冷和交感神经刺激诱导。Zfp516直接结合到UCP1启动子的近端区域,而非其他转录因子结合的增强子区域,并与PRDM16相互作用以激活UCP1启动子。尽管Zfp516的缺失会导致胚胎致死,但敲除胚胎的棕色脂肪组织质量仍显著降低。Zfp516在脂肪组织中的过表达即使在室温下也能促进iWAT的褐变,提高体温和能量消耗,并预防饮食诱导的肥胖。Zfp516可能成为肥胖治疗的未来靶点。