Tissue-Autonomous Function of Drosophila Seipin in Preventing Ectopic Lipid Droplet Formation

• DOI: 10.1371/journal.pgen.1001364
• Publication Date: 2011-04-14T20:53:52Z
• Authors: Yuan Tian; Junfeng Bi; Guanghou Shui; Zhonghua Liu; Yanhui Xiang; Yuan Liu; Markus R. Wenk; Hongyuan Yang; Xun Huang
• Keywords: Male; 0301 basic medicine; 570; Lipogenesis; Fat Body; Genetic Vectors; Phosphatidic Acids; QH426-470; Lipids; Salivary Glands; Disease Models, Animal; 03 medical and health sciences; Phenotype; Lipodystrophy, Congenital Generalized; GTP-Binding Protein gamma Subunits; Larva; Mutation; Genetics; Animals; Drosophila; RNA Interference; Obesity; Cells, Cultured; Research Article

Obesity is characterized by accumulation of excess body fat, while lipodystrophy is characterized by loss or absence of body fat. Despite their opposite phenotypes, these two conditions both cause ectopic lipid storage in non-adipose tissues, leading to lipotoxicity, which has health-threatening consequences. The exact mechanisms underlying ectopic lipid storage remain elusive. Here we report the analysis of a Drosophila model of the most severe form of human lipodystrophy, Berardinelli-Seip Congenital Lipodystrophy 2, which is caused by mutations in the BSCL2/Seipin gene. In addition to reduced lipid storage in the fat body, dSeipin mutant flies accumulate ectopic lipid droplets in the salivary gland, a non-adipose tissue. This phenotype was suppressed by expressing dSeipin specifically within the salivary gland. dSeipin mutants display synergistic genetic interactions with lipogenic genes in the formation of ectopic lipid droplets. Our data suggest that dSeipin may participate in phosphatidic acid metabolism and subsequently down-regulate lipogenesis to prevent ectopic lipid droplet formation. In summary, we have demonstrated a tissue-autonomous role of dSeipin in ectopic lipid storage in lipodystrophy.