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miR-29a Is Downregulated in Progenies Derived from Chronically Stressed Males

Recent research has provided compelling evidence demonstrating that paternal exposure to different stressors can influence their offspring’s phenotypes. We hypothesized that paternal stress can negatively impact the progeny, altering different miRs and triggering different physiological alterations...

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Detalles Bibliográficos
Autores principales: Riesco, Marta F., Valcarce, David G., Sellés-Egea, Alba, Esteve-Codina, Anna, Herráez, María Paz, Robles, Vanesa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531283/
https://www.ncbi.nlm.nih.gov/pubmed/37762407
http://dx.doi.org/10.3390/ijms241814107
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author Riesco, Marta F.
Valcarce, David G.
Sellés-Egea, Alba
Esteve-Codina, Anna
Herráez, María Paz
Robles, Vanesa
author_facet Riesco, Marta F.
Valcarce, David G.
Sellés-Egea, Alba
Esteve-Codina, Anna
Herráez, María Paz
Robles, Vanesa
author_sort Riesco, Marta F.
collection PubMed
description Recent research has provided compelling evidence demonstrating that paternal exposure to different stressors can influence their offspring’s phenotypes. We hypothesized that paternal stress can negatively impact the progeny, altering different miRs and triggering different physiological alterations that could compromise offspring development. To investigate this, we exposed zebrafish male siblings to a chronic stress protocol for 21 days. We performed RNA-sequencing (RNA-seq) analyses to identify differentially expressed small noncoding RNAs in 7-day postfertilization (dpf) larvae derived from paternally stressed males crossed with control females compared with the control progeny. We found a single miRNA differentially expressed—miR-29a—which was validated in larva and was also tested in the sperm, testicles, and brain of the stressed progenitors. We observed a vertical transmission of chronic stress to the unexposed larvae, reporting novel consequences of paternally inherited chronic stress at a molecular level. The deregulation of mi-R29a in those larvae could affect relevant biological processes affecting development, morphogenesis, or neurogenesis, among others. Additionally, these disruptions were associated with reduced rates of survival and hatching in the affected offspring.
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spelling pubmed-105312832023-09-28 miR-29a Is Downregulated in Progenies Derived from Chronically Stressed Males Riesco, Marta F. Valcarce, David G. Sellés-Egea, Alba Esteve-Codina, Anna Herráez, María Paz Robles, Vanesa Int J Mol Sci Article Recent research has provided compelling evidence demonstrating that paternal exposure to different stressors can influence their offspring’s phenotypes. We hypothesized that paternal stress can negatively impact the progeny, altering different miRs and triggering different physiological alterations that could compromise offspring development. To investigate this, we exposed zebrafish male siblings to a chronic stress protocol for 21 days. We performed RNA-sequencing (RNA-seq) analyses to identify differentially expressed small noncoding RNAs in 7-day postfertilization (dpf) larvae derived from paternally stressed males crossed with control females compared with the control progeny. We found a single miRNA differentially expressed—miR-29a—which was validated in larva and was also tested in the sperm, testicles, and brain of the stressed progenitors. We observed a vertical transmission of chronic stress to the unexposed larvae, reporting novel consequences of paternally inherited chronic stress at a molecular level. The deregulation of mi-R29a in those larvae could affect relevant biological processes affecting development, morphogenesis, or neurogenesis, among others. Additionally, these disruptions were associated with reduced rates of survival and hatching in the affected offspring. MDPI 2023-09-14 /pmc/articles/PMC10531283/ /pubmed/37762407 http://dx.doi.org/10.3390/ijms241814107 Text en © 2023 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 Article
Riesco, Marta F.
Valcarce, David G.
Sellés-Egea, Alba
Esteve-Codina, Anna
Herráez, María Paz
Robles, Vanesa
miR-29a Is Downregulated in Progenies Derived from Chronically Stressed Males
title miR-29a Is Downregulated in Progenies Derived from Chronically Stressed Males
title_full miR-29a Is Downregulated in Progenies Derived from Chronically Stressed Males
title_fullStr miR-29a Is Downregulated in Progenies Derived from Chronically Stressed Males
title_full_unstemmed miR-29a Is Downregulated in Progenies Derived from Chronically Stressed Males
title_short miR-29a Is Downregulated in Progenies Derived from Chronically Stressed Males
title_sort mir-29a is downregulated in progenies derived from chronically stressed males
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531283/
https://www.ncbi.nlm.nih.gov/pubmed/37762407
http://dx.doi.org/10.3390/ijms241814107
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