Functional genomic screen reveals genes involved in lipid-droplet formation and utilization

Nature. 2008 May 29;453(7195):657-61. doi: 10.1038/nature06928. Epub 2008 Apr 13.


Eukaryotic cells store neutral lipids in cytoplasmic lipid droplets enclosed in a monolayer of phospholipids and associated proteins. These dynamic organelles serve as the principal reservoirs for storing cellular energy and for the building blocks for membrane lipids. Excessive lipid accumulation in cells is a central feature of obesity, diabetes and atherosclerosis, yet remarkably little is known about lipid-droplet cell biology. Here we show, by means of a genome-wide RNA interference (RNAi) screen in Drosophila S2 cells that about 1.5% of all genes function in lipid-droplet formation and regulation. The phenotypes of the gene knockdowns sorted into five distinct phenotypic classes. Genes encoding enzymes of phospholipid biosynthesis proved to be determinants of lipid-droplet size and number, suggesting that the phospholipid composition of the monolayer profoundly affects droplet morphology and lipid utilization. A subset of the Arf1-COPI vesicular transport proteins also regulated droplet morphology and lipid utilization, thereby identifying a previously unrecognized function for this machinery. These phenotypes are conserved in mammalian cells, suggesting that insights from these studies are likely to be central to our understanding of human diseases involving excessive lipid storage.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADP-Ribosylation Factors / metabolism
  • Animals
  • Cell Line
  • Coat Protein Complex I / metabolism
  • Drosophila Proteins / genetics*
  • Drosophila melanogaster / cytology*
  • Drosophila melanogaster / genetics*
  • Genes, Insect / genetics*
  • Genome, Insect / genetics*
  • Genomics*
  • Lipid Metabolism / genetics*
  • Lipolysis
  • Phenotype
  • Phosphatidylcholines / metabolism
  • RNA Interference


  • Coat Protein Complex I
  • Drosophila Proteins
  • Phosphatidylcholines
  • ADP-Ribosylation Factors