Co-expression analysis of lncRNA and mRNA identifies potential adipogenesis regulatory non-coding RNAs involved in the transgenerational effects of tributyltin

Detalhes bibliográficos
Autor(a) principal: Lopes, Maria Fernanda da Silva [UNESP]
Data de Publicação: 2023
Outros Autores: Felix, Juliana de Souza [UNESP], Scaramele, Natália Francisco [UNESP], Almeida, Mariana Cordeiro [UNESP], Furlan, Amanda de Oliveira [UNESP], Troiano, Jéssica Antonini [UNESP], de Athayde, Flávia Regina Florêncio [UNESP], Lopes, Flávia Lombardi [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1371/journal.pone.0281240
http://hdl.handle.net/11449/246769
Resumo: The obesity epidemic is considered a global public health crisis, with an increase in caloric intake, sedentary lifestyles and/or genetic predispositions as contributing factors. Although the positive energy balance is one of the most significant causes of obesity, recent research has linked early exposure to Endocrine-Disrupting Chemicals (EDCs) such as the obesogen tributyltin (TBT) to the disease epidemic. In addition to their actions on the hormonal profile, EDCs can induce long-term changes in gene expression, possibly due to changes in epigenetic patterns. Long non-coding RNAs (lncRNAs) are epigenetic mediators that play important regulatory roles in several biological processes, through regulation of gene transcription and/or translation. In this study, we explored the differential expression of lncRNAs in gonadal white adipose tissue samples from adult male C57BL/6J F4 generation, female C57BL/6J offspring exposed (F0 generation) to 50 nM TBT or 0.1% DMSO (control of vehicle) via drinking water provided during pregnancy and lactation, analyzing RNA-seq data from a publicly available dataset (GSE105051). A total of 74 lncRNAs were differentially expressed (DE), 22 were up-regulated and 52 were down-regulated in the group whose F4 ancestor was exposed in utero to 50nM TBT when compared to those exposed to 0.1% DMSO (control). Regulation of DE lncRNAs and their potential partner genes in gonadal white adipose tissue of mice ancestrally exposed to EDC TBT may be related to the control of adipogenesis, as pathway enrichment analyses showed that these gene partners are mainly involved in the metabolism of lipids and glucose and in insulin-related pathways, which are essential for obesity onset and control.
id UNSP_0023bb8d90b6c5038dadfc08d673e4e8
oai_identifier_str oai:repositorio.unesp.br:11449/246769
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling Co-expression analysis of lncRNA and mRNA identifies potential adipogenesis regulatory non-coding RNAs involved in the transgenerational effects of tributyltinThe obesity epidemic is considered a global public health crisis, with an increase in caloric intake, sedentary lifestyles and/or genetic predispositions as contributing factors. Although the positive energy balance is one of the most significant causes of obesity, recent research has linked early exposure to Endocrine-Disrupting Chemicals (EDCs) such as the obesogen tributyltin (TBT) to the disease epidemic. In addition to their actions on the hormonal profile, EDCs can induce long-term changes in gene expression, possibly due to changes in epigenetic patterns. Long non-coding RNAs (lncRNAs) are epigenetic mediators that play important regulatory roles in several biological processes, through regulation of gene transcription and/or translation. In this study, we explored the differential expression of lncRNAs in gonadal white adipose tissue samples from adult male C57BL/6J F4 generation, female C57BL/6J offspring exposed (F0 generation) to 50 nM TBT or 0.1% DMSO (control of vehicle) via drinking water provided during pregnancy and lactation, analyzing RNA-seq data from a publicly available dataset (GSE105051). A total of 74 lncRNAs were differentially expressed (DE), 22 were up-regulated and 52 were down-regulated in the group whose F4 ancestor was exposed in utero to 50nM TBT when compared to those exposed to 0.1% DMSO (control). Regulation of DE lncRNAs and their potential partner genes in gonadal white adipose tissue of mice ancestrally exposed to EDC TBT may be related to the control of adipogenesis, as pathway enrichment analyses showed that these gene partners are mainly involved in the metabolism of lipids and glucose and in insulin-related pathways, which are essential for obesity onset and control.Department of Animal Production and Health School of Veterinary Medicine São Paulo State University Júlio de Mesquita Filho (Unesp)Faculdades de Dracena (UNIFADRA-Fundec)Department of Animal Production and Health School of Veterinary Medicine São Paulo State University Júlio de Mesquita Filho (Unesp)Universidade Estadual Paulista (UNESP)Faculdades de Dracena (UNIFADRA-Fundec)Lopes, Maria Fernanda da Silva [UNESP]Felix, Juliana de Souza [UNESP]Scaramele, Natália Francisco [UNESP]Almeida, Mariana Cordeiro [UNESP]Furlan, Amanda de Oliveira [UNESP]Troiano, Jéssica Antonini [UNESP]de Athayde, Flávia Regina Florêncio [UNESP]Lopes, Flávia Lombardi [UNESP]2023-07-29T12:50:03Z2023-07-29T12:50:03Z2023-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlee0281240http://dx.doi.org/10.1371/journal.pone.0281240PloS one, v. 18, n. 2, p. e0281240-, 2023.1932-6203http://hdl.handle.net/11449/24676910.1371/journal.pone.02812402-s2.0-85147457958Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPloS oneinfo:eu-repo/semantics/openAccess2023-07-29T12:50:03Zoai:repositorio.unesp.br:11449/246769Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-07-29T12:50:03Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Co-expression analysis of lncRNA and mRNA identifies potential adipogenesis regulatory non-coding RNAs involved in the transgenerational effects of tributyltin
title Co-expression analysis of lncRNA and mRNA identifies potential adipogenesis regulatory non-coding RNAs involved in the transgenerational effects of tributyltin
spellingShingle Co-expression analysis of lncRNA and mRNA identifies potential adipogenesis regulatory non-coding RNAs involved in the transgenerational effects of tributyltin
Lopes, Maria Fernanda da Silva [UNESP]
title_short Co-expression analysis of lncRNA and mRNA identifies potential adipogenesis regulatory non-coding RNAs involved in the transgenerational effects of tributyltin
title_full Co-expression analysis of lncRNA and mRNA identifies potential adipogenesis regulatory non-coding RNAs involved in the transgenerational effects of tributyltin
title_fullStr Co-expression analysis of lncRNA and mRNA identifies potential adipogenesis regulatory non-coding RNAs involved in the transgenerational effects of tributyltin
title_full_unstemmed Co-expression analysis of lncRNA and mRNA identifies potential adipogenesis regulatory non-coding RNAs involved in the transgenerational effects of tributyltin
title_sort Co-expression analysis of lncRNA and mRNA identifies potential adipogenesis regulatory non-coding RNAs involved in the transgenerational effects of tributyltin
author Lopes, Maria Fernanda da Silva [UNESP]
author_facet Lopes, Maria Fernanda da Silva [UNESP]
Felix, Juliana de Souza [UNESP]
Scaramele, Natália Francisco [UNESP]
Almeida, Mariana Cordeiro [UNESP]
Furlan, Amanda de Oliveira [UNESP]
Troiano, Jéssica Antonini [UNESP]
de Athayde, Flávia Regina Florêncio [UNESP]
Lopes, Flávia Lombardi [UNESP]
author_role author
author2 Felix, Juliana de Souza [UNESP]
Scaramele, Natália Francisco [UNESP]
Almeida, Mariana Cordeiro [UNESP]
Furlan, Amanda de Oliveira [UNESP]
Troiano, Jéssica Antonini [UNESP]
de Athayde, Flávia Regina Florêncio [UNESP]
Lopes, Flávia Lombardi [UNESP]
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
Faculdades de Dracena (UNIFADRA-Fundec)
dc.contributor.author.fl_str_mv Lopes, Maria Fernanda da Silva [UNESP]
Felix, Juliana de Souza [UNESP]
Scaramele, Natália Francisco [UNESP]
Almeida, Mariana Cordeiro [UNESP]
Furlan, Amanda de Oliveira [UNESP]
Troiano, Jéssica Antonini [UNESP]
de Athayde, Flávia Regina Florêncio [UNESP]
Lopes, Flávia Lombardi [UNESP]
description The obesity epidemic is considered a global public health crisis, with an increase in caloric intake, sedentary lifestyles and/or genetic predispositions as contributing factors. Although the positive energy balance is one of the most significant causes of obesity, recent research has linked early exposure to Endocrine-Disrupting Chemicals (EDCs) such as the obesogen tributyltin (TBT) to the disease epidemic. In addition to their actions on the hormonal profile, EDCs can induce long-term changes in gene expression, possibly due to changes in epigenetic patterns. Long non-coding RNAs (lncRNAs) are epigenetic mediators that play important regulatory roles in several biological processes, through regulation of gene transcription and/or translation. In this study, we explored the differential expression of lncRNAs in gonadal white adipose tissue samples from adult male C57BL/6J F4 generation, female C57BL/6J offspring exposed (F0 generation) to 50 nM TBT or 0.1% DMSO (control of vehicle) via drinking water provided during pregnancy and lactation, analyzing RNA-seq data from a publicly available dataset (GSE105051). A total of 74 lncRNAs were differentially expressed (DE), 22 were up-regulated and 52 were down-regulated in the group whose F4 ancestor was exposed in utero to 50nM TBT when compared to those exposed to 0.1% DMSO (control). Regulation of DE lncRNAs and their potential partner genes in gonadal white adipose tissue of mice ancestrally exposed to EDC TBT may be related to the control of adipogenesis, as pathway enrichment analyses showed that these gene partners are mainly involved in the metabolism of lipids and glucose and in insulin-related pathways, which are essential for obesity onset and control.
publishDate 2023
dc.date.none.fl_str_mv 2023-07-29T12:50:03Z
2023-07-29T12:50:03Z
2023-01-01
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/10.1371/journal.pone.0281240
PloS one, v. 18, n. 2, p. e0281240-, 2023.
1932-6203
http://hdl.handle.net/11449/246769
10.1371/journal.pone.0281240
2-s2.0-85147457958
url http://dx.doi.org/10.1371/journal.pone.0281240
http://hdl.handle.net/11449/246769
identifier_str_mv PloS one, v. 18, n. 2, p. e0281240-, 2023.
1932-6203
10.1371/journal.pone.0281240
2-s2.0-85147457958
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv PloS one
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv e0281240
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
_version_ 1803650138520944640