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Nuclear-Mitochondrial Interactions
Mitochondria, the cell’s major energy producers, also act as signaling hubs, interacting with other organelles both directly and indirectly. Despite having its own circular genome, the majority of mitochondrial proteins are encoded by nuclear DNA. To respond to changes in cell physiology, the mitoch...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8946195/ https://www.ncbi.nlm.nih.gov/pubmed/35327619 http://dx.doi.org/10.3390/biom12030427 |
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author | Walker, Brittni R. Moraes, Carlos T. |
author_facet | Walker, Brittni R. Moraes, Carlos T. |
author_sort | Walker, Brittni R. |
collection | PubMed |
description | Mitochondria, the cell’s major energy producers, also act as signaling hubs, interacting with other organelles both directly and indirectly. Despite having its own circular genome, the majority of mitochondrial proteins are encoded by nuclear DNA. To respond to changes in cell physiology, the mitochondria must send signals to the nucleus, which can, in turn, upregulate gene expression to alter metabolism or initiate a stress response. This is known as retrograde signaling. A variety of stimuli and pathways fall under the retrograde signaling umbrella. Mitochondrial dysfunction has already been shown to have severe implications for human health. Disruption of retrograde signaling, whether directly associated with mitochondrial dysfunction or cellular environmental changes, may also contribute to pathological deficits. In this review, we discuss known signaling pathways between the mitochondria and the nucleus, examine the possibility of direct contacts, and identify pathological consequences of an altered relationship. |
format | Online Article Text |
id | pubmed-8946195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89461952022-03-25 Nuclear-Mitochondrial Interactions Walker, Brittni R. Moraes, Carlos T. Biomolecules Review Mitochondria, the cell’s major energy producers, also act as signaling hubs, interacting with other organelles both directly and indirectly. Despite having its own circular genome, the majority of mitochondrial proteins are encoded by nuclear DNA. To respond to changes in cell physiology, the mitochondria must send signals to the nucleus, which can, in turn, upregulate gene expression to alter metabolism or initiate a stress response. This is known as retrograde signaling. A variety of stimuli and pathways fall under the retrograde signaling umbrella. Mitochondrial dysfunction has already been shown to have severe implications for human health. Disruption of retrograde signaling, whether directly associated with mitochondrial dysfunction or cellular environmental changes, may also contribute to pathological deficits. In this review, we discuss known signaling pathways between the mitochondria and the nucleus, examine the possibility of direct contacts, and identify pathological consequences of an altered relationship. MDPI 2022-03-10 /pmc/articles/PMC8946195/ /pubmed/35327619 http://dx.doi.org/10.3390/biom12030427 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Walker, Brittni R. Moraes, Carlos T. Nuclear-Mitochondrial Interactions |
title | Nuclear-Mitochondrial Interactions |
title_full | Nuclear-Mitochondrial Interactions |
title_fullStr | Nuclear-Mitochondrial Interactions |
title_full_unstemmed | Nuclear-Mitochondrial Interactions |
title_short | Nuclear-Mitochondrial Interactions |
title_sort | nuclear-mitochondrial interactions |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8946195/ https://www.ncbi.nlm.nih.gov/pubmed/35327619 http://dx.doi.org/10.3390/biom12030427 |
work_keys_str_mv | AT walkerbrittnir nuclearmitochondrialinteractions AT moraescarlost nuclearmitochondrialinteractions |