SLC25A39 is necessary for mitochondrial glutathione import in mammalian cells Journal Article


Authors: Wang, Y.; Yen, F. S.; Zhu, X. G.; Timson, R. C.; Weber, R.; Xing, C.; Liu, Y.; Allwein, B.; Luo, H.; Yeh, H. W.; Heissel, S.; Unlu, G.; Gamazon, E. R.; Kharas, M. G.; Hite, R.; Birsoy, K.
Article Title: SLC25A39 is necessary for mitochondrial glutathione import in mammalian cells
Abstract: Glutathione (GSH) is a small-molecule thiol that is abundant in all eukaryotes and has key roles in oxidative metabolism1. Mitochondria, as the major site of oxidative reactions, must maintain sufficient levels of GSH to perform protective and biosynthetic functions2. GSH is synthesized exclusively in the cytosol, yet the molecular machinery involved in mitochondrial GSH import remains unknown. Here, using organellar proteomics and metabolomics approaches, we identify SLC25A39, a mitochondrial membrane carrier of unknown function, as a regulator of GSH transport into mitochondria. Loss of SLC25A39 reduces mitochondrial GSH import and abundance without affecting cellular GSH levels. Cells lacking both SLC25A39 and its paralogue SLC25A40 exhibit defects in the activity and stability of proteins containing iron–sulfur clusters. We find that mitochondrial GSH import is necessary for cell proliferation in vitro and red blood cell development in mice. Heterologous expression of an engineered bifunctional bacterial GSH biosynthetic enzyme (GshF) in mitochondria enables mitochondrial GSH production and ameliorates the metabolic and proliferative defects caused by its depletion. Finally, GSH availability negatively regulates SLC25A39 protein abundance, coupling redox homeostasis to mitochondrial GSH import in mammalian cells. Our work identifies SLC25A39 as an essential and regulated component of the mitochondrial GSH-import machinery. © 2021, The Author(s), under exclusive licence to Springer Nature Limited.
Keywords: mammalia; bacteria (microorganisms); eukaryota; homeostasis; mitochondrion; machinery; membrane; coupling; abundance
Journal Title: Nature
Volume: 599
ISSN: 0028-0836
Publisher: Nature Publishing Group  
Date Published: 2021-11-04
Start Page: 136
End Page: 140
Language: English
DOI: 10.1038/s41586-021-04025-w
PROVIDER: scopus
PUBMED: 34707288
PMCID: PMC10981497
DOI/URL:
Notes: Article -- Export Date: 1 December 2021 -- Source: Scopus
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors
  1. Michael Kharas
    96 Kharas
  2. Richard Kevin Hite
    25 Hite
  3. Hanzhi Luo
    22 Luo
  4. Changrui Xing
    1 Xing