Mitochondrial microRNAs: A Putative Role in Tissue Regeneration

The most famous role of mitochondria is to generate ATP through oxidative phosphorylation, a metabolic pathway that involves a chain of four protein complexes (the electron transport chain, ETC) that generates a proton-motive force that in turn drives the ATP synthesis by the Complex V (ATP synthase...

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Main Authors: Sílvia C. Rodrigues, Renato M. S. Cardoso, Filipe V. Duarte
Format: Article
Language:English
Published: MDPI AG 2020-12-01
Series:Biology
Subjects:
Online Access:https://www.mdpi.com/2079-7737/9/12/486
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spelling doaj-b4849318d0c5444e9859403c6735bafc2020-12-22T00:06:05ZengMDPI AGBiology2079-77372020-12-01948648610.3390/biology9120486Mitochondrial microRNAs: A Putative Role in Tissue RegenerationSílvia C. Rodrigues0Renato M. S. Cardoso1Filipe V. Duarte2Exogenus Therapeutics, 3060-197 Cantanhede, PortugalLaserLeap Technologies, 3025-307 Coimbra, PortugalCNC—Center for Neuroscience and Cell Biology, University of Coimbra, 3004-504 Coimbra, PortugalThe most famous role of mitochondria is to generate ATP through oxidative phosphorylation, a metabolic pathway that involves a chain of four protein complexes (the electron transport chain, ETC) that generates a proton-motive force that in turn drives the ATP synthesis by the Complex V (ATP synthase). An impressive number of more than 1000 mitochondrial proteins have been discovered. Since mitochondrial proteins have a dual genetic origin, it is predicted that ~99% of these proteins are nuclear-encoded and are synthesized in the cytoplasmatic compartment, being further imported through mitochondrial membrane transporters. The lasting 1% of mitochondrial proteins are encoded by the mitochondrial genome and synthesized by the mitochondrial ribosome (mitoribosome). As a result, an appropriate regulation of mitochondrial protein synthesis is absolutely required to achieve and maintain normal mitochondrial function. Regarding miRNAs in mitochondria, it is well-recognized nowadays that several cellular mechanisms involving mitochondria are regulated by many genetic players that originate from either nuclear- or mitochondrial-encoded small noncoding RNAs (sncRNAs). Growing evidence collected from whole genome and transcriptome sequencing highlight the role of distinct members of this class, from short interfering RNAs (siRNAs) to miRNAs and long noncoding RNAs (lncRNAs). Some of the mechanisms that have been shown to be modulated are the expression of mitochondrial proteins itself, as well as the more complex coordination of mitochondrial structure and dynamics with its function. We devote particular attention to the role of mitochondrial miRNAs and to their role in the modulation of several molecular processes that could ultimately contribute to tissue regeneration accomplishment.https://www.mdpi.com/2079-7737/9/12/486microRNAmitochondriamitomiRstissue regeneration
collection DOAJ
language English
format Article
sources DOAJ
author Sílvia C. Rodrigues
Renato M. S. Cardoso
Filipe V. Duarte
spellingShingle Sílvia C. Rodrigues
Renato M. S. Cardoso
Filipe V. Duarte
Mitochondrial microRNAs: A Putative Role in Tissue Regeneration
Biology
microRNA
mitochondria
mitomiRs
tissue regeneration
author_facet Sílvia C. Rodrigues
Renato M. S. Cardoso
Filipe V. Duarte
author_sort Sílvia C. Rodrigues
title Mitochondrial microRNAs: A Putative Role in Tissue Regeneration
title_short Mitochondrial microRNAs: A Putative Role in Tissue Regeneration
title_full Mitochondrial microRNAs: A Putative Role in Tissue Regeneration
title_fullStr Mitochondrial microRNAs: A Putative Role in Tissue Regeneration
title_full_unstemmed Mitochondrial microRNAs: A Putative Role in Tissue Regeneration
title_sort mitochondrial micrornas: a putative role in tissue regeneration
publisher MDPI AG
series Biology
issn 2079-7737
publishDate 2020-12-01
description The most famous role of mitochondria is to generate ATP through oxidative phosphorylation, a metabolic pathway that involves a chain of four protein complexes (the electron transport chain, ETC) that generates a proton-motive force that in turn drives the ATP synthesis by the Complex V (ATP synthase). An impressive number of more than 1000 mitochondrial proteins have been discovered. Since mitochondrial proteins have a dual genetic origin, it is predicted that ~99% of these proteins are nuclear-encoded and are synthesized in the cytoplasmatic compartment, being further imported through mitochondrial membrane transporters. The lasting 1% of mitochondrial proteins are encoded by the mitochondrial genome and synthesized by the mitochondrial ribosome (mitoribosome). As a result, an appropriate regulation of mitochondrial protein synthesis is absolutely required to achieve and maintain normal mitochondrial function. Regarding miRNAs in mitochondria, it is well-recognized nowadays that several cellular mechanisms involving mitochondria are regulated by many genetic players that originate from either nuclear- or mitochondrial-encoded small noncoding RNAs (sncRNAs). Growing evidence collected from whole genome and transcriptome sequencing highlight the role of distinct members of this class, from short interfering RNAs (siRNAs) to miRNAs and long noncoding RNAs (lncRNAs). Some of the mechanisms that have been shown to be modulated are the expression of mitochondrial proteins itself, as well as the more complex coordination of mitochondrial structure and dynamics with its function. We devote particular attention to the role of mitochondrial miRNAs and to their role in the modulation of several molecular processes that could ultimately contribute to tissue regeneration accomplishment.
topic microRNA
mitochondria
mitomiRs
tissue regeneration
url https://www.mdpi.com/2079-7737/9/12/486
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