Transcriptomics of the late gestation ovine fetal brain: modeling the co-expression of immune marker genes

Autores
Rabaglino, Maria Belen; Keller Wood, Maureen; Wood, Charles E.
Año de publicación
2014
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Background: Major changes in gene expression occur in the fetal brain to modulate the function of this organ postnatally. Thus, factors can alter the genomics of the fetal brain, predisposing to neurological disorders later in life. We hypothesized that the physiological dynamics of the immune system transcriptome of the fetal brain during the last stage of gestation will reveal patterns of immune function and development in the developing brain. In this study we applied weighted gene co-expression analysis of microarrays performed on ovine fetal brain samples, to model the changes in gene expression throughout the second half of gestation. Results: Clusters of co-expressed genes that strongly increase in expression toward the first day of extra-uterine life are related to the hematopoietic lineage, while activation of immune pathways is induced after birth. Moreover, the pattern of gene expression suggests induction of tolerance mechanisms, probably necessary to protect highly produced proteins –such as myelin basic protein- from an autoimmune attack. Conclusions: This study provides insight into the dramatic changes in gene expression that take place in the brain during the fetal life, especially during the last stage of gestation, and suggests that the immune system may have an important role in maturation of the fetal brain, which if disrupted or altered, could have negative consequences in postnatal life.
Fil: Rabaglino, Maria Belen. Universidad Nacional de Río Cuarto. Facultad de Agronomía y Veterinaria; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina
Fil: Keller Wood, Maureen. University of Florida; Estados Unidos
Fil: Wood, Charles E.. University of Florida; Estados Unidos
Materia
FETAL BRAIN
MICROARRAY
HEMATOPOIESIS
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/35035

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network_name_str CONICET Digital (CONICET)
spelling Transcriptomics of the late gestation ovine fetal brain: modeling the co-expression of immune marker genesRabaglino, Maria BelenKeller Wood, MaureenWood, Charles E.FETAL BRAINMICROARRAYHEMATOPOIESIShttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Background: Major changes in gene expression occur in the fetal brain to modulate the function of this organ postnatally. Thus, factors can alter the genomics of the fetal brain, predisposing to neurological disorders later in life. We hypothesized that the physiological dynamics of the immune system transcriptome of the fetal brain during the last stage of gestation will reveal patterns of immune function and development in the developing brain. In this study we applied weighted gene co-expression analysis of microarrays performed on ovine fetal brain samples, to model the changes in gene expression throughout the second half of gestation. Results: Clusters of co-expressed genes that strongly increase in expression toward the first day of extra-uterine life are related to the hematopoietic lineage, while activation of immune pathways is induced after birth. Moreover, the pattern of gene expression suggests induction of tolerance mechanisms, probably necessary to protect highly produced proteins –such as myelin basic protein- from an autoimmune attack. Conclusions: This study provides insight into the dramatic changes in gene expression that take place in the brain during the fetal life, especially during the last stage of gestation, and suggests that the immune system may have an important role in maturation of the fetal brain, which if disrupted or altered, could have negative consequences in postnatal life.Fil: Rabaglino, Maria Belen. Universidad Nacional de Río Cuarto. Facultad de Agronomía y Veterinaria; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; ArgentinaFil: Keller Wood, Maureen. University of Florida; Estados UnidosFil: Wood, Charles E.. University of Florida; Estados UnidosBioMed Central2014-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/35035Rabaglino, Maria Belen; Keller Wood, Maureen; Wood, Charles E.; Transcriptomics of the late gestation ovine fetal brain: modeling the co-expression of immune marker genes; BioMed Central; BMC Genomics; 15; 11-2014; 1-91471-2164CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://bmcgenomics.biomedcentral.com/articles/10.1186/1471-2164-15-1001info:eu-repo/semantics/altIdentifier/doi/10.1186/1471-2164-15-1001info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:06:29Zoai:ri.conicet.gov.ar:11336/35035instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:06:29.314CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Transcriptomics of the late gestation ovine fetal brain: modeling the co-expression of immune marker genes
title Transcriptomics of the late gestation ovine fetal brain: modeling the co-expression of immune marker genes
spellingShingle Transcriptomics of the late gestation ovine fetal brain: modeling the co-expression of immune marker genes
Rabaglino, Maria Belen
FETAL BRAIN
MICROARRAY
HEMATOPOIESIS
title_short Transcriptomics of the late gestation ovine fetal brain: modeling the co-expression of immune marker genes
title_full Transcriptomics of the late gestation ovine fetal brain: modeling the co-expression of immune marker genes
title_fullStr Transcriptomics of the late gestation ovine fetal brain: modeling the co-expression of immune marker genes
title_full_unstemmed Transcriptomics of the late gestation ovine fetal brain: modeling the co-expression of immune marker genes
title_sort Transcriptomics of the late gestation ovine fetal brain: modeling the co-expression of immune marker genes
dc.creator.none.fl_str_mv Rabaglino, Maria Belen
Keller Wood, Maureen
Wood, Charles E.
author Rabaglino, Maria Belen
author_facet Rabaglino, Maria Belen
Keller Wood, Maureen
Wood, Charles E.
author_role author
author2 Keller Wood, Maureen
Wood, Charles E.
author2_role author
author
dc.subject.none.fl_str_mv FETAL BRAIN
MICROARRAY
HEMATOPOIESIS
topic FETAL BRAIN
MICROARRAY
HEMATOPOIESIS
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Background: Major changes in gene expression occur in the fetal brain to modulate the function of this organ postnatally. Thus, factors can alter the genomics of the fetal brain, predisposing to neurological disorders later in life. We hypothesized that the physiological dynamics of the immune system transcriptome of the fetal brain during the last stage of gestation will reveal patterns of immune function and development in the developing brain. In this study we applied weighted gene co-expression analysis of microarrays performed on ovine fetal brain samples, to model the changes in gene expression throughout the second half of gestation. Results: Clusters of co-expressed genes that strongly increase in expression toward the first day of extra-uterine life are related to the hematopoietic lineage, while activation of immune pathways is induced after birth. Moreover, the pattern of gene expression suggests induction of tolerance mechanisms, probably necessary to protect highly produced proteins –such as myelin basic protein- from an autoimmune attack. Conclusions: This study provides insight into the dramatic changes in gene expression that take place in the brain during the fetal life, especially during the last stage of gestation, and suggests that the immune system may have an important role in maturation of the fetal brain, which if disrupted or altered, could have negative consequences in postnatal life.
Fil: Rabaglino, Maria Belen. Universidad Nacional de Río Cuarto. Facultad de Agronomía y Veterinaria; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina
Fil: Keller Wood, Maureen. University of Florida; Estados Unidos
Fil: Wood, Charles E.. University of Florida; Estados Unidos
description Background: Major changes in gene expression occur in the fetal brain to modulate the function of this organ postnatally. Thus, factors can alter the genomics of the fetal brain, predisposing to neurological disorders later in life. We hypothesized that the physiological dynamics of the immune system transcriptome of the fetal brain during the last stage of gestation will reveal patterns of immune function and development in the developing brain. In this study we applied weighted gene co-expression analysis of microarrays performed on ovine fetal brain samples, to model the changes in gene expression throughout the second half of gestation. Results: Clusters of co-expressed genes that strongly increase in expression toward the first day of extra-uterine life are related to the hematopoietic lineage, while activation of immune pathways is induced after birth. Moreover, the pattern of gene expression suggests induction of tolerance mechanisms, probably necessary to protect highly produced proteins –such as myelin basic protein- from an autoimmune attack. Conclusions: This study provides insight into the dramatic changes in gene expression that take place in the brain during the fetal life, especially during the last stage of gestation, and suggests that the immune system may have an important role in maturation of the fetal brain, which if disrupted or altered, could have negative consequences in postnatal life.
publishDate 2014
dc.date.none.fl_str_mv 2014-11
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/35035
Rabaglino, Maria Belen; Keller Wood, Maureen; Wood, Charles E.; Transcriptomics of the late gestation ovine fetal brain: modeling the co-expression of immune marker genes; BioMed Central; BMC Genomics; 15; 11-2014; 1-9
1471-2164
CONICET Digital
CONICET
url http://hdl.handle.net/11336/35035
identifier_str_mv Rabaglino, Maria Belen; Keller Wood, Maureen; Wood, Charles E.; Transcriptomics of the late gestation ovine fetal brain: modeling the co-expression of immune marker genes; BioMed Central; BMC Genomics; 15; 11-2014; 1-9
1471-2164
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://bmcgenomics.biomedcentral.com/articles/10.1186/1471-2164-15-1001
info:eu-repo/semantics/altIdentifier/doi/10.1186/1471-2164-15-1001
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv BioMed Central
publisher.none.fl_str_mv BioMed Central
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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