4.6 Article

Promethin Is a Conserved Seipin Partner Protein

Journal

CELLS
Volume 8, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/cells8030268

Keywords

promethin; TMEM159; seipin; BSCL2; SPG17; lipid droplet; LD; lipodystrophy; LDO; adipogenesis

Categories

Funding

  1. Deutsche Forschungsgemeinschaft (DFG), Cells-in-Motion Cluster of Excellence, University of Munster, Germany [EXC 1003-CiM]
  2. DFG [SFB1190]
  3. Volkswagen Stiftung Life Grant [93092]
  4. Medical Research Council [MR/L002620/1]
  5. Biotechnology and Biological Sciences Research Council [BB/K017772/1]
  6. EMBO Long-term Fellowship [ALTF-580-2017]
  7. Azrieli Foundation
  8. BBSRC [BB/K017772/1] Funding Source: UKRI
  9. MRC [MR/L002620/1] Funding Source: UKRI

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Seipin (BSCL2/SPG17) is a key factor in lipid droplet (LD) biology, and its dysfunction results in severe pathologies, including the fat storage disease Berardinelli-Seip congenital lipodystrophy type 2, as well as several neurological seipinopathies. Despite its importance for human health, the molecular role of seipin is still enigmatic. Seipin is evolutionarily conserved from yeast to humans. In yeast, seipin was recently found to cooperate with the lipid droplet organization (LDO) proteins, Ldo16 and Ldo45, two structurally-related proteins involved in LD function and identity that display remote homology to the human protein promethin/TMEM159. In this study, we show that promethin is indeed an LD-associated protein that forms a complex with seipin, and its localization to the LD surface can be modulated by seipin expression levels. We thus identify promethin as a novel seipin partner protein.

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