Cited by 57Mitochondrial Function and PathologyAutophagy in Disease and TherapyMetabolism, Diabetes, and Cancer

The DOI matches its Crossref record; 355 of the 359 references it cites were found in a registry or an index.

Decoding the rosetta stone of mitonuclear communication

Open access

Abstract

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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Crossref · 10.1016/j.phrs.2020.105161

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  1. Muller, 1942, Isolating mechanisms, evolution, and temperature, Biol. Symp., 71

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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)
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
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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