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Unraveling mitochondrial piRNAs in mouse embryonic gonadal cells
Although mitochondria are widely studied organelles, the recent interest in the role of mitochondrial small noncoding RNAs (sncRNAs), miRNAs, and more recently, piRNAs, is providing new functional perspectives in germ cell development and differentiation. piRNAs (PIWI-interacting RNAs) are single-st...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9232517/ https://www.ncbi.nlm.nih.gov/pubmed/35750721 http://dx.doi.org/10.1038/s41598-022-14414-4 |
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author | Barreñada, Odei Larriba, Eduardo Fernández-Pérez, Daniel Brieño-Enríquez, Miguel Ángel del Mazo Martínez, Jesús |
author_facet | Barreñada, Odei Larriba, Eduardo Fernández-Pérez, Daniel Brieño-Enríquez, Miguel Ángel del Mazo Martínez, Jesús |
author_sort | Barreñada, Odei |
collection | PubMed |
description | Although mitochondria are widely studied organelles, the recent interest in the role of mitochondrial small noncoding RNAs (sncRNAs), miRNAs, and more recently, piRNAs, is providing new functional perspectives in germ cell development and differentiation. piRNAs (PIWI-interacting RNAs) are single-stranded sncRNAs of mostly about 20–35 nucleotides, generated from the processing of pre-piRNAs. We leverage next-generation sequencing data obtained from mouse primordial germ cells and somatic cells purified from early-differentiating embryonic ovaries and testis from 11.5 to 13.5 days postcoitum. Using bioinformatic tools, we elucidate (i) the origins of piRNAs as transcribed from mitochondrial DNA fragments inserted in the nucleus or from the mitochondrial genome; (ii) their levels of expression; and (iii) their potential roles, as well as their association with genomic regions encoding other sncRNAs (such as tRNAs and rRNAs) and the mitochondrial regulatory region (D-loop). Finally, our results suggest how nucleo-mitochondrial communication, both anterograde and retrograde signaling, may be mediated by mitochondria-associated piRNAs. |
format | Online Article Text |
id | pubmed-9232517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-92325172022-06-26 Unraveling mitochondrial piRNAs in mouse embryonic gonadal cells Barreñada, Odei Larriba, Eduardo Fernández-Pérez, Daniel Brieño-Enríquez, Miguel Ángel del Mazo Martínez, Jesús Sci Rep Article Although mitochondria are widely studied organelles, the recent interest in the role of mitochondrial small noncoding RNAs (sncRNAs), miRNAs, and more recently, piRNAs, is providing new functional perspectives in germ cell development and differentiation. piRNAs (PIWI-interacting RNAs) are single-stranded sncRNAs of mostly about 20–35 nucleotides, generated from the processing of pre-piRNAs. We leverage next-generation sequencing data obtained from mouse primordial germ cells and somatic cells purified from early-differentiating embryonic ovaries and testis from 11.5 to 13.5 days postcoitum. Using bioinformatic tools, we elucidate (i) the origins of piRNAs as transcribed from mitochondrial DNA fragments inserted in the nucleus or from the mitochondrial genome; (ii) their levels of expression; and (iii) their potential roles, as well as their association with genomic regions encoding other sncRNAs (such as tRNAs and rRNAs) and the mitochondrial regulatory region (D-loop). Finally, our results suggest how nucleo-mitochondrial communication, both anterograde and retrograde signaling, may be mediated by mitochondria-associated piRNAs. Nature Publishing Group UK 2022-06-24 /pmc/articles/PMC9232517/ /pubmed/35750721 http://dx.doi.org/10.1038/s41598-022-14414-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Barreñada, Odei Larriba, Eduardo Fernández-Pérez, Daniel Brieño-Enríquez, Miguel Ángel del Mazo Martínez, Jesús Unraveling mitochondrial piRNAs in mouse embryonic gonadal cells |
title | Unraveling mitochondrial piRNAs in mouse embryonic gonadal cells |
title_full | Unraveling mitochondrial piRNAs in mouse embryonic gonadal cells |
title_fullStr | Unraveling mitochondrial piRNAs in mouse embryonic gonadal cells |
title_full_unstemmed | Unraveling mitochondrial piRNAs in mouse embryonic gonadal cells |
title_short | Unraveling mitochondrial piRNAs in mouse embryonic gonadal cells |
title_sort | unraveling mitochondrial pirnas in mouse embryonic gonadal cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9232517/ https://www.ncbi.nlm.nih.gov/pubmed/35750721 http://dx.doi.org/10.1038/s41598-022-14414-4 |
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