Fld1p, a functional homologue of human seipin, regulates the size of lipid droplets in yeast

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Abstract
Lipid droplets (LDs) are emerging cellular organelles that are of crucial importance in cell biology and human diseases. In this study, we present our screen of 4,700 Saccharomyces cerevisiae mutants for abnormalities in the number and morphology of LDs; we identify 17 fld (few LDs) and 116 mld (many LDs) mutants. One of the fld mutants (fld1) is caused by the deletion of YLR404W, a previously uncharacterized open reading frame. Cells lacking FLD1 contain strikingly enlarged (supersized) LDs, and LDs from fld1 Delta cells demonstrate significantly enhanced fusion activities both in vivo and in vitro. Interestingly, the expression of human seipin, whose mutant forms are associated with Berardinelli-Seip congenital lipodystrophy and motoneuron disorders, rescues LD-associated defects in fld1 Delta cells. Lipid profiling reveals alterations in acyl chain compositions of major phospholipids in fld1 Delta cells. These results suggest that an evolutionally conserved function of seipin in phospholipid metabolism and LD formation may be functionally important in human adipogenesis.
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Author(s)
Fei, W
Shui, G
Gaeta, Bruno
Du, Xi
Kuerschner, L
Brown, Andrew
Wenk, M
Parton, R
Yang, Hyuk-Seung
Li, Peng
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Publication Year
2008
Resource Type
Journal Article
Degree Type
UNSW Faculty