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Selection of references for quantitative real-time PCR analysis of microRNAs in Nile tilapia (Oreochromis niloticus) under osmotic stress

Bibliographic Details
Main Author: Martins, Amanda W.S.
Publication Date: 2024
Other Authors: Nunes, Leandro S., Blödorn, Eduardo B., Dellagostin, Eduardo N., Silveira, Tony L.R., Collares, Gilberto L., Domingues, William B., Pinhal, Danillo [UNESP], Remião, Mariana H., Campos, Vinicius F.
Format: Article
Language: eng
Source: Repositório Institucional da UNESP
Download full: http://dx.doi.org/10.1016/j.cbpb.2024.111010
https://hdl.handle.net/11449/301709
Summary: MicroRNAs play crucial regulatory roles in various aspects of development and physiology, including environmental adaptation and stress responses in teleosts. RT-qPCR is the most commonly used method for studying microRNA expression, with the accuracy and reliability of results depending on the use of an appropriate reference gene for normalization. This study aimed to evaluate seven miRNAs (U6, Let-7a, miR-23a, miR-25-3, miR-103, miR-99-5, and miR-455) expression stability in different tissues of Nile tilapia subjected to osmotic stress. Fish were divided into two groups: a control and an experimental group, raised in 0 and 12 ppt salinity water respectively. After 21 days, brain, gills, liver, and posterior intestine were collected for analysis. Different mathematical algorithms (geNorm, NormFinder, BestKeeper, and the comparative ΔCt method) were employed to identify the most suitable reference miRNAs. The results indicate that the miR-455/miR-23a combination is a robust reference for normalizing miRNA expression levels in studies of osmotic stress responses in Nile tilapia. The stability of miRNA expression can vary depending on specific stress conditions and biological processes, underscoring the necessity of selecting appropriate normalizing miRNAs for each experimental context. This study identifies reliable reference genes for future RT-qPCR analyses of miRNA expression, thereby enhancing our understanding of molecular responses in fish to environmental challenges. These insights are fundamental to the development of new technologies for the improved management and sustainability of aquaculture practices.
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spelling Selection of references for quantitative real-time PCR analysis of microRNAs in Nile tilapia (Oreochromis niloticus) under osmotic stressChronic stressGene expressionqPCRReference miRNASalinityMicroRNAs play crucial regulatory roles in various aspects of development and physiology, including environmental adaptation and stress responses in teleosts. RT-qPCR is the most commonly used method for studying microRNA expression, with the accuracy and reliability of results depending on the use of an appropriate reference gene for normalization. This study aimed to evaluate seven miRNAs (U6, Let-7a, miR-23a, miR-25-3, miR-103, miR-99-5, and miR-455) expression stability in different tissues of Nile tilapia subjected to osmotic stress. Fish were divided into two groups: a control and an experimental group, raised in 0 and 12 ppt salinity water respectively. After 21 days, brain, gills, liver, and posterior intestine were collected for analysis. Different mathematical algorithms (geNorm, NormFinder, BestKeeper, and the comparative ΔCt method) were employed to identify the most suitable reference miRNAs. The results indicate that the miR-455/miR-23a combination is a robust reference for normalizing miRNA expression levels in studies of osmotic stress responses in Nile tilapia. The stability of miRNA expression can vary depending on specific stress conditions and biological processes, underscoring the necessity of selecting appropriate normalizing miRNAs for each experimental context. This study identifies reliable reference genes for future RT-qPCR analyses of miRNA expression, thereby enhancing our understanding of molecular responses in fish to environmental challenges. These insights are fundamental to the development of new technologies for the improved management and sustainability of aquaculture practices.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado do Rio Grande do SulLaboratório de Genômica Estrutural Programa de Pós-Graduação em Biotecnologia Centro de Desenvolvimento Tecnológico Universidade Federal de Pelotas, RSInstituto de Biologia Universidade Federal de Pelotas, RSAgência de Desenvolvimento da Bacia da Lagoa Mirim Universidade Federal de Pelotas, RSLaboratório Genômica e Evolução Molecular Instituto de Biociências de Botucatu Departamento de Genética – Universidade Estadual Paulista, SPLaboratório Genômica e Evolução Molecular Instituto de Biociências de Botucatu Departamento de Genética – Universidade Estadual Paulista, SPUniversidade Federal de PelotasUniversidade Estadual Paulista (UNESP)Martins, Amanda W.S.Nunes, Leandro S.Blödorn, Eduardo B.Dellagostin, Eduardo N.Silveira, Tony L.R.Collares, Gilberto L.Domingues, William B.Pinhal, Danillo [UNESP]Remião, Mariana H.Campos, Vinicius F.2025-04-29T18:59:05Z2024-10-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1016/j.cbpb.2024.111010Comparative Biochemistry and Physiology Part - B: Biochemistry and Molecular Biology, v. 274.1879-11071096-4959https://hdl.handle.net/11449/30170910.1016/j.cbpb.2024.1110102-s2.0-85200122053Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengComparative Biochemistry and Physiology Part - B: Biochemistry and Molecular Biologyinfo:eu-repo/semantics/openAccess2025-10-23T14:24:12Zoai:repositorio.unesp.br:11449/301709Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-10-23T14:24:12Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Selection of references for quantitative real-time PCR analysis of microRNAs in Nile tilapia (Oreochromis niloticus) under osmotic stress
title Selection of references for quantitative real-time PCR analysis of microRNAs in Nile tilapia (Oreochromis niloticus) under osmotic stress
spellingShingle Selection of references for quantitative real-time PCR analysis of microRNAs in Nile tilapia (Oreochromis niloticus) under osmotic stress
Martins, Amanda W.S.
Chronic stress
Gene expression
qPCR
Reference miRNA
Salinity
title_short Selection of references for quantitative real-time PCR analysis of microRNAs in Nile tilapia (Oreochromis niloticus) under osmotic stress
title_full Selection of references for quantitative real-time PCR analysis of microRNAs in Nile tilapia (Oreochromis niloticus) under osmotic stress
title_fullStr Selection of references for quantitative real-time PCR analysis of microRNAs in Nile tilapia (Oreochromis niloticus) under osmotic stress
title_full_unstemmed Selection of references for quantitative real-time PCR analysis of microRNAs in Nile tilapia (Oreochromis niloticus) under osmotic stress
title_sort Selection of references for quantitative real-time PCR analysis of microRNAs in Nile tilapia (Oreochromis niloticus) under osmotic stress
author Martins, Amanda W.S.
author_facet Martins, Amanda W.S.
Nunes, Leandro S.
Blödorn, Eduardo B.
Dellagostin, Eduardo N.
Silveira, Tony L.R.
Collares, Gilberto L.
Domingues, William B.
Pinhal, Danillo [UNESP]
Remião, Mariana H.
Campos, Vinicius F.
author_role author
author2 Nunes, Leandro S.
Blödorn, Eduardo B.
Dellagostin, Eduardo N.
Silveira, Tony L.R.
Collares, Gilberto L.
Domingues, William B.
Pinhal, Danillo [UNESP]
Remião, Mariana H.
Campos, Vinicius F.
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de Pelotas
Universidade Estadual Paulista (UNESP)
dc.contributor.author.fl_str_mv Martins, Amanda W.S.
Nunes, Leandro S.
Blödorn, Eduardo B.
Dellagostin, Eduardo N.
Silveira, Tony L.R.
Collares, Gilberto L.
Domingues, William B.
Pinhal, Danillo [UNESP]
Remião, Mariana H.
Campos, Vinicius F.
dc.subject.por.fl_str_mv Chronic stress
Gene expression
qPCR
Reference miRNA
Salinity
topic Chronic stress
Gene expression
qPCR
Reference miRNA
Salinity
description MicroRNAs play crucial regulatory roles in various aspects of development and physiology, including environmental adaptation and stress responses in teleosts. RT-qPCR is the most commonly used method for studying microRNA expression, with the accuracy and reliability of results depending on the use of an appropriate reference gene for normalization. This study aimed to evaluate seven miRNAs (U6, Let-7a, miR-23a, miR-25-3, miR-103, miR-99-5, and miR-455) expression stability in different tissues of Nile tilapia subjected to osmotic stress. Fish were divided into two groups: a control and an experimental group, raised in 0 and 12 ppt salinity water respectively. After 21 days, brain, gills, liver, and posterior intestine were collected for analysis. Different mathematical algorithms (geNorm, NormFinder, BestKeeper, and the comparative ΔCt method) were employed to identify the most suitable reference miRNAs. The results indicate that the miR-455/miR-23a combination is a robust reference for normalizing miRNA expression levels in studies of osmotic stress responses in Nile tilapia. The stability of miRNA expression can vary depending on specific stress conditions and biological processes, underscoring the necessity of selecting appropriate normalizing miRNAs for each experimental context. This study identifies reliable reference genes for future RT-qPCR analyses of miRNA expression, thereby enhancing our understanding of molecular responses in fish to environmental challenges. These insights are fundamental to the development of new technologies for the improved management and sustainability of aquaculture practices.
publishDate 2024
dc.date.none.fl_str_mv 2024-10-01
2025-04-29T18:59:05Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.cbpb.2024.111010
Comparative Biochemistry and Physiology Part - B: Biochemistry and Molecular Biology, v. 274.
1879-1107
1096-4959
https://hdl.handle.net/11449/301709
10.1016/j.cbpb.2024.111010
2-s2.0-85200122053
url http://dx.doi.org/10.1016/j.cbpb.2024.111010
https://hdl.handle.net/11449/301709
identifier_str_mv Comparative Biochemistry and Physiology Part - B: Biochemistry and Molecular Biology, v. 274.
1879-1107
1096-4959
10.1016/j.cbpb.2024.111010
2-s2.0-85200122053
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Comparative Biochemistry and Physiology Part - B: Biochemistry and Molecular Biology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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