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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/35035
Ver los metadatos del registro completo
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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 |
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CONICET Digital (CONICET) |
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CONICET Digital (CONICET) |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
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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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13.13397 |