Author
Listed:
- Ayenachew Bezawork-Geleta
(Griffith University
Queensland Brain Institute, University of Queensland)
- He Wen
(Shenzhen University School of Medicine
Natural Product Research Institute, Seoul National University)
- LanFeng Dong
(Griffith University)
- Bing Yan
(Griffith University)
- Jelena Vider
(Griffith University)
- Stepana Boukalova
(Czech Academy of Sciences)
- Linda Krobova
(Czech Academy of Sciences)
- Katerina Vanova
(Czech Academy of Sciences)
- Renata Zobalova
(Czech Academy of Sciences)
- Margarita Sobol
(Czech Academy of Sciences)
- Pavel Hozak
(Czech Academy of Sciences)
- Silvia Magalhaes Novais
(Czech Academy of Sciences)
- Veronika Caisova
(Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health
University of South Bohemia)
- Pavel Abaffy
(Czech Academy of Sciences)
- Ravindra Naraine
(Czech Academy of Sciences)
- Ying Pang
(Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health)
- Thiri Zaw
(Macquarie University)
- Ping Zhang
(Griffith University)
- Radek Sindelka
(Czech Academy of Sciences)
- Mikael Kubista
(Czech Academy of Sciences
TATAA Biocenter)
- Steven Zuryn
(Queensland Brain Institute, University of Queensland)
- Mark P. Molloy
(Macquarie University)
- Michael V. Berridge
(Malaghan Institute of Medical Research)
- Karel Pacak
(Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health)
- Jakub Rohlena
(Czech Academy of Sciences)
- Sunghyouk Park
(Natural Product Research Institute, Seoul National University)
- Jiri Neuzil
(Griffith University
Czech Academy of Sciences)
Abstract
Cell growth and survival depend on a delicate balance between energy production and synthesis of metabolites. Here, we provide evidence that an alternative mitochondrial complex II (CII) assembly, designated as CIIlow, serves as a checkpoint for metabolite biosynthesis under bioenergetic stress, with cells suppressing their energy utilization by modulating DNA synthesis and cell cycle progression. Depletion of CIIlow leads to an imbalance in energy utilization and metabolite synthesis, as evidenced by recovery of the de novo pyrimidine pathway and unlocking cell cycle arrest from the S-phase. In vitro experiments are further corroborated by analysis of paraganglioma tissues from patients with sporadic, SDHA and SDHB mutations. These findings suggest that CIIlow is a core complex inside mitochondria that provides homeostatic control of cellular metabolism depending on the availability of energy.
Suggested Citation
Ayenachew Bezawork-Geleta & He Wen & LanFeng Dong & Bing Yan & Jelena Vider & Stepana Boukalova & Linda Krobova & Katerina Vanova & Renata Zobalova & Margarita Sobol & Pavel Hozak & Silvia Magalhaes N, 2018.
"Alternative assembly of respiratory complex II connects energy stress to metabolic checkpoints,"
Nature Communications, Nature, vol. 9(1), pages 1-17, December.
Handle:
RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-04603-z
DOI: 10.1038/s41467-018-04603-z
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