4.3 Article

A Genetic Screen for Mutants with Supersized Lipid Droplets in Caenorhabditis elegans

Journal

G3-GENES GENOMES GENETICS
Volume 6, Issue 8, Pages 2407-2419

Publisher

GENETICS SOCIETY AMERICA
DOI: 10.1534/g3.116.030866

Keywords

C. elegans; lipid droplet; peroxisome; forward genetic screen; drop

Funding

  1. National Institutes of Health (NIH) Office of Research Infrastructure Programs [P40 OD010440]
  2. MITANI Laboratory through the National Bio-Resource Project of the MEXT, Japan
  3. International Exchange and Joint Training Grant of the Graduate School of Capital Normal University (CNU)
  4. CNU
  5. National Natural Science Foundation of China [31370820]
  6. Beijing Municipal Education Commission [KZ201410028032]

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To identify genes that regulate the dynamics of lipid droplet (LD) size, we have used the genetically tractable model organism Caenorhabditis elegans, whose wild-type LD population displays a steady state of size with an upper limit of 3 mu m in diameter. From a saturated forward genetic screen of 6.7 x 10(5) mutagenized haploid genomes, we isolated 118 mutants with supersized intestinal LDs often reaching 10 mu m. These mutants define nine novel complementation groups, in addition to four known genes (maoc-1, dhs-28, daf-22, and prx-10). The nine groups are named drop (lipid droplet abnormal) and categorized into four classes. Class I mutants drop-5 and drop-9, similar to prx-10, are up-regulated in ACS-22-DGAT-2-dependent LD growth, resistant to LD hydrolysis, and defective in peroxisome import. Class II mutants drop-2, drop-3, drop-6, and drop-7 are up-regulated in LD growth, are resistant to LD hydrolysis, but are not defective in peroxisome import. Class III mutants drop-1 and drop-8 are neither up-regulated in LD growth nor resistant to LD hydrolysis, but seemingly up-regulated in LD fusion. Class IV mutant drop-4 is cloned as sams-1 and, different to the other three classes, is ACS-22-independent and hydrolysis-resistant. These four classes of supersized LD mutants should be valuable for mechanistic studies of LD cellular processes including growth, hydrolysis, and fusion.

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