Suh Jae Myoung, Zeve Daniel, McKay Renee, Seo Jin, Salo Zack, Li Robert, Wang Michael, Graff Jonathan M
Department of Developmental Biology, University of Texas Southwestern Medical Center, 6000 Harry Hines Boulevard, NB5.118, Dallas, TX 75390-9133, USA.
Cell Metab. 2007 Sep;6(3):195-207. doi: 10.1016/j.cmet.2007.08.001.
Adipose (Adp) is an evolutionarily conserved gene isolated from naturally occurring obese flies homozygous for an adp mutation. Here we show that the anti-obesity function of Adp (worm Y73E7A.9, fly adp, and murine Wdtc1) is conserved from worms to mammals. Further, Adp appears to inhibit fat formation in a dosage-sensitive manner. Adp heterozygous flies and Adp heterozygous mutant mice are obese and insulin resistant, as are mice that express a dominant negative form of Adp in fat cells. Conversely, fat-restricted Adp transgenic mice are lean and display improved metabolic profiles. A transient transgenic increase in Adp activity in adult fly fat tissues reduces fat accumulation, indicating therapeutic potential. ADP may elicit these anti-adipogenic functions by regulating chromatin dynamics and gene transcription, as it binds both histones and HDAC3 and inhibits PPARgamma activity. Thus Adp appears to be involved in an ancient pathway that regulates fat accumulation.
脂肪(Adp)是从因adp突变而纯合的天然肥胖果蝇中分离出的一个进化上保守的基因。我们在此表明,Adp(线虫Y73E7A.9、果蝇adp和小鼠Wdtc1)的抗肥胖功能从线虫到哺乳动物都是保守的。此外,Adp似乎以剂量敏感的方式抑制脂肪形成。Adp杂合果蝇和Adp杂合突变小鼠肥胖且具有胰岛素抵抗,在脂肪细胞中表达Adp显性负性形式的小鼠也是如此。相反,脂肪特异性Adp转基因小鼠体型瘦且代谢状况改善。成年果蝇脂肪组织中Adp活性的短暂转基因增加会减少脂肪积累,表明其具有治疗潜力。ADP可能通过调节染色质动态和基因转录来引发这些抗脂肪生成功能,因为它既能结合组蛋白又能结合HDAC3并抑制PPARγ活性。因此,Adp似乎参与了一条调节脂肪积累的古老途径。