Formation of giant ER sheets by pentadecanoic acid causes lipotoxicity in fission yeast

Y Yojiro Hoshikawa (Department of Biotechnology, Graduate School of Agricultural and Life Sciences, The University of Tokyo) N Natsuho Shirota (Food Science Program, School of Applied Biological Science, Hiroshima University) H Hiroshi Tsugawa (Department of Biotechnology and Life Science, Tokyo University of Agriculture and Technology) S Satoshi Kimura (Department of Laboratory Medicine and Central Clinical Laboratory) A Akihisa Matsuyama (Department of Biotechnology, Graduate School of Agricultural and Life Sciences, The University of Tokyo) Y Yoko Yashiroda (Molecular Ligand Target Research Team/Chemical Genomics Research Group, RIKEN Center for Sustainable Resource Science) H Hideaki Kakeya (Division of Medicinal Frontier Sciences, Graduate School of Pharmaceutical Sciences, Kyoto University) M Makoto Arita R Reiko Iizumi (Center for Marine Biotechnology and Biomedicine, Scripps Institution of Oceanography, University of California San Diego) M Minoru Yoshida (Department of Biotechnology, Graduate School of Agricultural and Life Sciences, The University of Tokyo) S Shinichi Nishimura (Department of Biotechnology, Graduate School of Agricultural and Life Sciences, The University of Tokyo)

Abstract

Excess amounts of saturated fatty acids (FAs) are toxic to organisms, a condition termed lipotoxicity, which is often accompanied by pleiotropic cellular and tissue dysfunction. Here, we show that pentadecanoic acid (C15:0) exerts toxicity on the fission yeast Schizosaccharomyces pombe by generating an aberrantly planar endoplasmic reticulum (ER) structure, which we named a “giant ER sheet.” Untargeted lipidomics revealed that C15:0 is incorporated into complex lipids depending on an acyl-CoA ligase Lcf1 and an acyl-CoA transferase Slc1, thereby increasing the saturation level of the acyl chains. The toxicity and giant ER sheet formation were abolished by deleting lcf1 or slc1 gene, indicating that the incorporation of C15:0 into glycerophospholipids causes giant ER sheet formation. The giant ER sheets disrupted the correct migration of Mid1, a protein determining the cell division site, and physically blocked septum formation, hindering correct cell separation. Our results suggest that the ER is the primary site targeted by saturated FAs, leading to lipotoxicity.

Article Details

Volume / Issue Vol. 122, Issue 22
Published June 03, 2025
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (11)

Y

Yojiro Hoshikawa

Department of Biotechnology, Graduate School of Agricultural and Life Sciences, The University of Tokyo

N

Natsuho Shirota

Food Science Program, School of Applied Biological Science, Hiroshima University

H

Hiroshi Tsugawa

Department of Biotechnology and Life Science, Tokyo University of Agriculture and Technology

S

Satoshi Kimura

Department of Laboratory Medicine and Central Clinical Laboratory

A

Akihisa Matsuyama

Department of Biotechnology, Graduate School of Agricultural and Life Sciences, The University of Tokyo

Y

Yoko Yashiroda

Molecular Ligand Target Research Team/Chemical Genomics Research Group, RIKEN Center for Sustainable Resource Science

H

Hideaki Kakeya

Division of Medicinal Frontier Sciences, Graduate School of Pharmaceutical Sciences, Kyoto University

M

Makoto Arita

R

Reiko Iizumi

Center for Marine Biotechnology and Biomedicine, Scripps Institution of Oceanography, University of California San Diego

M

Minoru Yoshida

Department of Biotechnology, Graduate School of Agricultural and Life Sciences, The University of Tokyo

S

Shinichi Nishimura

Department of Biotechnology, Graduate School of Agricultural and Life Sciences, The University of Tokyo