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Decoding the rosetta stone of mitonuclear communication
Open accessAbstract
Cellular homeostasis in eukaryotic cells requires synchronized coordination of multiple organelles. A key role in this stage is played by mitochondria, which have recently emerged as highly interconnected and multifunctional hubs that process and coordinate diverse cellular functions. Beyond producing ATP, mitochondria generate key metabolites and are central to apoptotic and metabolic signaling pathways. Because most mitochondrial proteins are encoded in the nuclear genome, the biogenesis of new mitochondria and the maintenance of mitochondrial functions and flexibility critically depend upon effective mitonuclear communication. This review addresses the complex network of signaling molecules and pathways allowing mitochondria-nuclear communication and coordinated regulation of their independent but interconnected genomes, and discusses the extent to which dynamic communication between the two organelles has evolved for mutual benefit and for the overall maintenance of cellular and organismal fitness.
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“The human homolog of Rtg3p is the microphthalmia-associated transcription factor (MITF) (Goding and Arnheiter 2019), which is not involved in mitonuclear signaling that in Metazoa evolved independently and uses different mechanisms (Butow and Avadhani 2004; Jazwinski 2014; English et al. 2020).”
From Mitochondrial retrograde control of transcription evolves with respiratory stress, metabolic adaptation, and virulence in budding yeasts (2026) · cites this paper as English et al. 2020
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“The human homolog of Rtg3p is the microphthalmia-associated transcription factor (MITF) (Goding and Arnheiter 2019), which is not involved in mitonuclear signaling that in Metazoa evolved independently and uses different mechanisms (Butow and Avadhani 2004; Jazwinski 2014; English et al. 2020).”
From Mitochondrial retrograde control of transcription evolves with respiratory stress, metabolic adaptation, and virulence in budding yeasts (2026) · cites this paper as English et al. 2020
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Mitochondrial retrograde signaling regulates neuronal function
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Role of transcription factor acetylation in the regulation of metabolic homeostasis
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Salubrinal protects against rotenone-induced SH-SY5Y cell death via ATF4-parkin pathway
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NAD+ Metabolism and NAD+-Dependent Enzymes: Promising Therapeutic Targets for Neurological Diseases
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Mitochondrial sirtuins and metabolic homeostasis
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Skeletal Muscle Nucleo-Mitochondrial Crosstalk in Obesity and Type 2 Diabetes
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SOD2 and the Mitochondrial UPR: Partners Regulating Cellular Phenotypic Transitions
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Mitochondrial UPR: A Double-Edged Sword
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SUMO-specific Protease 1 Regulates Mitochondrial Biogenesis through PGC-1α
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Mitochondrial retrograde signaling in the nervous system
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Effects of Mitochondrial-Derived Peptides (MDPs) on Mitochondrial and Cellular Health in AMD
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Exploring the In Vivo Role of the Mitochondrial Calcium Uniporter in Brown Fat Bioenergetics
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mtDNA, Metastasis, and the Mitochondrial Unfolded Protein Response (UPRmt)
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Rtg2 protein: At the nexus of yeast longevity and aging
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Mitochondrial-nuclear DNA mismatch matters
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Mitochondrial retrograde signalling in neurological disease
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A selection system for human apoptosis inhibitors using yeast
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Innate Immune Recognition of mtDNA—An Undercover Signal?
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Lysine-Specific Demethylase 2 Suppresses Lipid Influx and Metabolism in Hepatic Cells
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A single biochemical activity underlies the pleiotropy of the aging-related protein CLK-1
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FoxO1 localizes to mitochondria of adipose tissue and is affected by nutrient stress
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Sirtuins: potential therapeutic targets for regulating acute inflammatory response?
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Changes in specific lipids regulate BAX‐induced mitochondrial permeability transition
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A nuclear sensor of mitochondrial function
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Mitochondrial-to-nuclear communication in aging: an epigenetic perspective
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Cnm1 mediates nucleus–mitochondria contact site formation in response to phospholipid levels
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The molecular pathology of pathogenic mitochondrial tRNA variants
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Socialized mitochondria: mitonuclear crosstalk in stress
Kim, K. H., & Lee, C. B. (2024) · Experimental & Molecular Medicine · doi:10.1038/s12276-024-01211-4 · Cited by 62
Self-citationEmerging roles of mitochondrial functions and epigenetic changes in the modulation of stem cell fate
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Metadata
- Authors
- English, J., Son, J. M., Cardamone, M. D., Lee, C., & Perissi, V.
- Affiliations
- Boston University (US)
- University of Southern California (US)
- Corresponding author
- Perissi, Valentina
- Venue
- Pharmacological Research
- Publisher
- Elsevier BV
- Published
- 2020-11
- Volume
- 161
- Pages
- 105161
- ISSN
- 1043-6618 (ISSN-L)
- PMC
- PMC7755734
- OpenAlex
- W3081296598
- Cited by
- 55
- References
- 359
- Citations by year
- 2026: 10 · 2025: 7 · 2024: 17 · 2023: 8 · 2022: 4 · 2021: 8 · 2020: 1
- FWCI
- 0.50
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Pharmacological Research (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- NIH (R01GM127625, 5T32GM008541)
- VP, NIH (R01AG052258)
- AFAR fellowship
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- mitochondria, nuclear genome, mitochondrial biogenesis, cellular homeostasis, mitochondrial pathway, mitochondrial metabolism, apoptosis, organelle evolution
- MeSH terms
- Animals, Cell Communication, Cell Nucleus, Gene Expression Regulation, Humans, Mitochondria, Nuclear Proteins, Signal Transduction, Mitochondrial Proteins
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