Yeast growth in raffinose results in resistance to acetic acid induced programmed cell death mostly due to the activation of the mitochondrial retrograde pathway
Open accessAbstract
In order to investigate whether and how a modification of mitochondrial metabolism can affect yeast sensitivity to programmed cell death (PCD) induced by acetic acid (AA-PCD), yeast cells were grown on raffinose, as a sole carbon source, which, differently from glucose, favours mitochondrial respiration. We found that, differently from glucose-grown cells, raffinose-grown cells were mostly resistant to AA-PCD and that this was due to the activation of mitochondrial retrograde (RTG) response, which increased with time, as revealed by the up-regulation of the peroxisomal isoform of citrate synthase and isocitrate dehydrogenase isoform 1, RTG pathway target genes. Accordingly, the deletion of RTG2 and RTG3, a positive regulator and a transcription factor of the RTG pathway, resulted in AA-PCD, as shown by TUNEL assay. Neither deletion in raffinose-grown cells of HAP4, encoding the positive regulatory subunit of the Hap2,3,4,5 complex nor constitutive activation of the RTG pathway in glucose-grown cells due to deletion of MKS1, a negative regulator of RTG pathway, had effect on yeast AA-PCD. The RTG pathway was found to be activated in yeast cells containing mitochondria, in which membrane potential was measured, capable to consume oxygen in a manner stimulated by the uncoupler CCCP and inhibited by the respiratory chain inhibitor antimycin A. AA-PCD resistance in raffinose-grown cells occurs with a decrease in both ROS production and cytochrome c release as compared to glucose-grown cells en route to AA-PCD.
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Guaragnella, N., Ždralević, M., Palková, Z., & Giannattasio, S. (2021) · Methods in molecular biology · doi:10.1007/978-1-0716-1266-8_6 · Cited by 3 · see citing works
Self-citationDynamic assembly of malate dehydrogenase–citrate synthase multienzyme complex in the mitochondriaPreprint
Omini, J. J., Krassovskaya, I., Dele-Osibanjo, T. A., Pedersen, C., & Obata, T. (2025) · eLife · doi:10.7554/elife.107953 · Cited by 3 · see citing works
Primavera, A., Laera, L., Castegna, A., Scarcia, P., Palmieri, L., Noia, M. A. D., & Guaragnella, N. (2025) · Biochemical Journal · doi:10.1042/bcj20253414 · Cited by 2 · see citing works
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Self-citationŁabędzka-Dmoch, K., Bui, T. H. D., Piątkowski, J., Dilling, M., Jagiełło, P., Kabza, W., & Golik, P. (2026) · Molecular Biology and Evolution · doi:10.1093/molbev/msag005 · Cited by 1 · see citing works
Druseikis, M. E., & Covo, S. (2024) · Yeast · doi:10.1002/yea.3975 · Cited by 1 · see citing works
Saputro, S. S. T., Wahyunita, K., Nurhasanah, A., Nugraha, Y., Faizal, I., Pambudi, S., & Pramono, A. P. (2023) · F1000Research · doi:10.12688/f1000research.123181.1 · Cited by 1 · see citing works
Druseikis, M. E., & Covo, S. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.21.481281
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Singh, M. K., Cavellini, L., Kunz, C., Lelek, M., Bomme, P., Belgareh‐Touzé, N., Mallet, A., Dietrich, L., Zimmer, C., & Cohen, M. M. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.03.21.582105
Saputro, S. S. T., Wahyunita, K., Nurhasanah, A., Nugraha, Y., Faizal, I., Pambudi, S., & Pramono, A. P. (2024) · F1000Research · doi:10.12688/f1000research.123181.2
Saputro, S. S. T., Wahyunita, K., Nurhasanah, A., Nugraha, Y., Faizal, I., Pambudi, S., Wibowo, S., & Pramono, A. P. (2024) · F1000Research · doi:10.12688/f1000research.123181.3
Dynamic assembly of malate dehydrogenase–citrate synthase multienzyme complex in the mitochondria
Omini, J. J., Krassovskaya, I., Dele-Osibanjo, T. A., Pedersen, C., & Obata, T. (2026) · eLife · doi:10.7554/elife.107953.3
Dynamic assembly of malate dehydrogenase-citrate synthase multienzyme complex in the mitochondriaPreprint
Omini, J. J., Krassovskaya, I., Dele-Osibanjo, T. A., Pedersen, C., & Obata, T. (2025) · eLife · doi:10.7554/elife.107953.1
Modeling premature aging in yeast via the expression of Progerin
Belak, Z. R., Ptak, C., Harris, R. E., Wozniak, R., Eskiw, C. H., & Harkness, T. A. A. (2026) · Aging · doi:10.18632/aging.206367
A 25+ Year Journey on Yeast-Regulated Cell Death Research
Sousa, M. J., Rego, A., Martins, V. M., Santos‐Pereira, C., Chaves, S. R., & Côrte‐Real, M. (2026) · Current topics in microbiology and immunology · doi:10.1007/82_2026_342
Druseikis, M., & Covo, S. (2026) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkag261
- Authors
- Guaragnella, N., Ždralević, M., Lattanzio, P., Marzulli, D., Pracheil, T., Liu, Z., Passarella, S., Marra, E., & Giannattasio, S.
- Affiliations
- Institute of Biomembranes, Bioenergetics and Molecular Biotechnologies (IT)
- LSU New Orleans (US)
- University of Molise (IT)
- Corresponding author
- Giannattasio, Sergio
- ORCID
- Venue
- Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
- Publisher
- Elsevier BV
- Published
- 2013-12
- Volume
- 1833
- Issue
- 12
- Pages
- 2765-2774
- ISSN
- 0167-4889 (ISSN-L)
- OpenAlex
- W2009721804
- Cited by
- 52
- References
- 62
- Citations by year
- 2026: 6 · 2025: 5 · 2024: 6 · 2023: 2 · 2022: 3 · 2021: 7 · 2019: 3 · 2018: 2 · 2017: 3 · 2016: 6 · 2015: 4 · 2014: 4 · 2013: 1
- FWCI
- 2.24
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Biochimica et Biophysica Acta (BBA) - Molecular Cell Research (publishedVersion)
- PubMed (publishedVersion)
- CINECA IRIS Institutional Research Information System (University of Bari Aldo Moro) (submittedVersion)
- Funders
- FIRB-MERIT RBNE08HWLZ
- Italian Ministry of Economy and Finance
- University of Salento
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Keywords
- raffinose, yeast, mitochondrial respiration, peroxisome biogenesis, citrate synthase, isocitrate dehydrogenase, HAP4, MKS1, reactive oxygen species, cytochrome c release, mitochondrial membrane potential, carbon source
- MeSH terms
- Glucose, Hydrogen-Ion Concentration, Mitochondria, Phosphorylation, Raffinose, Saccharomyces cerevisiae, Immunoblotting, Signal Transduction, Apoptosis, Gene Deletion, Reactive Oxygen Species, Acetic Acid, Saccharomyces cerevisiae Proteins, Intracellular Space, Cytochromes c, Membrane Potential, Mitochondrial
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