Mitochondria-cytosol-nucleus crosstalk: learning from Saccharomyces cerevisiae
Open accessAbstract
Mitochondria are key cell organelles with a prominent role in both energetic metabolism and the maintenance of cellular homeostasis. Since mitochondria harbor their own genome, which encodes a limited number of proteins critical for oxidative phosphorylation and protein translation, their function and biogenesis strictly depend upon nuclear control. The yeast Saccharomyces cerevisiae has been a unique model for understanding mitochondrial DNA organization and inheritance as well as for deciphering the process of assembly of mitochondrial components. In the last three decades, yeast also provided a powerful tool for unveiling the communication network that coordinates the functions of the nucleus, the cytosol and mitochondria. This crosstalk regulates how cells respond to extra- and intracellular changes either to maintain cellular homeostasis or to activate cell death. This review is focused on the key pathways that mediate nucleus-cytosol-mitochondria communications through both transcriptional regulation and proteostatic signaling. We aim to highlight yeast that likely continues to serve as a productive model organism for mitochondrial research in the years to come.
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Only two C. albicans Rtg targets, DIC1 and PEX11, were found to be upregulated in respiratory-deficient strains of S. cerevisiae, albeit in a manner that does not depend on the Rtg transcription factors.
“Yet, only two of them—DIC1 and PEX11 were found to be upregulated in respiratory-deficient strains of S. cerevisiae, albeit in a manner that does not depend on the Rtg transcription factors (Epstein et al. 2001; Guaragnella et al. 2018).”
From Mitochondrial retrograde control of transcription evolves with respiratory stress, metabolic adaptation, and virulence in budding yeasts (2026) · cites this paper as Guaragnella et al. 2018
The section on RTG-independent retrograde signaling describes upregulation of ATO3 in cells lacking mitochondrial DNA, while the section on mitochondria–nucleus communication describes broader transcriptional changes during respiratory deficiency. Neither passage identifies DIC1 or PEX11, establishes that they are C. albicans Rtg targets, or addresses whether their upregulation in S. cerevisiae is independent of Rtg transcription factors (searched: DIC1, PEX11, C. albicans Rtg targets). Page numbers were not available in our copy. (LLM, conf=0.72)
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- Authors
- Guaragnella, N., Coyne, L. P., Chen, X. J., & Giannattasio, S.
- Affiliations
- Institute of Biomembranes, Bioenergetics and Molecular Biotechnologies (IT)
- SUNY Upstate Medical University (US)
- Corresponding author
- Chen, Xin Jie
- Giannattasio, Sergio
- Venue
- FEMS Yeast Research
- Publisher
- Oxford University Press (OUP)
- Published
- 2018-08-03
- Volume
- 18
- Issue
- 8
- ISSN
- 1567-1356 (ISSN-L)
- 1567-1364
- PMC
- PMC6110143
- OpenAlex
- W2886049585
- Cited by
- 72
- References
- 169
- Citations by year
- 2026: 7 · 2025: 5 · 2024: 7 · 2023: 8 · 2022: 13 · 2021: 11 · 2020: 12 · 2019: 8 · 2018: 1
- FWCI
- 0.78
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- FEMS Yeast Research (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- CINECA IRIS Institutional Research Information System (University of Bari Aldo Moro) (submittedVersion)
- Funders
- National Institutes of Health (AG023731, AG047400)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
- Keywords
- mitochondrial DNA, Saccharomyces cerevisiae, mitochondrial biogenesis, oxidative phosphorylation, transcriptional regulation, cellular homeostasis, cell death, mitochondrial inheritance, organelle communication
- MeSH terms
- Cell Nucleus, Cytosol, Mitochondria, Saccharomyces cerevisiae, Stress, Physiological, Gene Regulatory Networks
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