Allele-specific expression analysis reveals conserved and unique features of preimplantation development in equine ICSI embryos

Autores
Goszczynski, Daniel Estanislao; Tinetti, P. S.; Choi, Y. H.; Ross, Pablo Juan; Hinrichs, K.
Año de publicación
2021
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Embryonic genome activation and dosage compensation are major genetic events in early development. Combined analysis of single embryo RNA-seq data and parental genome sequencing was used to evaluate parental contributions to early development and investigate X-chromosome dynamics. In addition, we evaluated dimorphism in gene expression between male and female embryos. Evaluation of parent-specific gene expression revealed a minor increase in paternal expression at the 4-cell stage that increased at the 8-cell stage. We also detected eight genes with allelic expression bias that may have an important role in early development, notably NANOGNB. The main actor in X-chromosome inactivation, XIST, was significantly upregulated at the 8-cell, morula, and blastocyst stages in female embryos, with high expression at the latter. Sexual dimorphism in gene expression was identified at all stages, with strong representation of the X-chromosome in females from the 16-cell to the blastocyst stage. Female embryos showed biparental X-chromosome expression at all stages after the 4-cell stage, demonstrating the absence of imprinted X-inactivation at the embryo level. The analysis of gene dosage showed incomplete dosage compensation (0.5 < X:A < 1) in MII oocytes and embryos up to the 4-cell stage, an increase of the X:A ratio at the 16-cell and morula stages after genome activation, and a decrease of the X:A ratio at the blastocyst stage, which might be associated with the beginning of X-chromosome inactivation. This study represents the first critical analysis of parent- and sex-specific gene expression in early equine embryos produced in vitro.
Fil: Goszczynski, Daniel Estanislao. University of California at Davis; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico CONICET- La Plata. Instituto de Genética Veterinaria "Ing. Fernando Noel Dulout". Universidad Nacional de La Plata. Facultad de Ciencias Veterinarias. Instituto de Genética Veterinaria; Argentina
Fil: Tinetti, P. S.. Texas A&M University; Estados Unidos
Fil: Choi, Y. H.. Texas A&M University; Estados Unidos
Fil: Ross, Pablo Juan. University of California at Davis; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Hinrichs, K.. Texas A&M University; Estados Unidos
Materia
HORSE GENOME ACTIVATION
DOSAGE COMPENSATION
X-CHROMOSOME INACTIVATION
ALLELIC BIAS
ICSI
SEXUAL DIMORPHISM
GENE EXPRESSION
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:11336/158083

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network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Allele-specific expression analysis reveals conserved and unique features of preimplantation development in equine ICSI embryosGoszczynski, Daniel EstanislaoTinetti, P. S.Choi, Y. H.Ross, Pablo JuanHinrichs, K.HORSE GENOME ACTIVATIONDOSAGE COMPENSATIONX-CHROMOSOME INACTIVATIONALLELIC BIASICSISEXUAL DIMORPHISMGENE EXPRESSIONhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Embryonic genome activation and dosage compensation are major genetic events in early development. Combined analysis of single embryo RNA-seq data and parental genome sequencing was used to evaluate parental contributions to early development and investigate X-chromosome dynamics. In addition, we evaluated dimorphism in gene expression between male and female embryos. Evaluation of parent-specific gene expression revealed a minor increase in paternal expression at the 4-cell stage that increased at the 8-cell stage. We also detected eight genes with allelic expression bias that may have an important role in early development, notably NANOGNB. The main actor in X-chromosome inactivation, XIST, was significantly upregulated at the 8-cell, morula, and blastocyst stages in female embryos, with high expression at the latter. Sexual dimorphism in gene expression was identified at all stages, with strong representation of the X-chromosome in females from the 16-cell to the blastocyst stage. Female embryos showed biparental X-chromosome expression at all stages after the 4-cell stage, demonstrating the absence of imprinted X-inactivation at the embryo level. The analysis of gene dosage showed incomplete dosage compensation (0.5 < X:A < 1) in MII oocytes and embryos up to the 4-cell stage, an increase of the X:A ratio at the 16-cell and morula stages after genome activation, and a decrease of the X:A ratio at the blastocyst stage, which might be associated with the beginning of X-chromosome inactivation. This study represents the first critical analysis of parent- and sex-specific gene expression in early equine embryos produced in vitro.Fil: Goszczynski, Daniel Estanislao. University of California at Davis; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico CONICET- La Plata. Instituto de Genética Veterinaria "Ing. Fernando Noel Dulout". Universidad Nacional de La Plata. Facultad de Ciencias Veterinarias. Instituto de Genética Veterinaria; ArgentinaFil: Tinetti, P. S.. Texas A&M University; Estados UnidosFil: Choi, Y. H.. Texas A&M University; Estados UnidosFil: Ross, Pablo Juan. University of California at Davis; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Hinrichs, K.. Texas A&M University; Estados UnidosSociety for the Study of Reproduction2021-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/158083Goszczynski, Daniel Estanislao; Tinetti, P. S.; Choi, Y. H.; Ross, Pablo Juan; Hinrichs, K.; Allele-specific expression analysis reveals conserved and unique features of preimplantation development in equine ICSI embryos; Society for the Study of Reproduction; Biology of Reproduction; 105; 6; 9-2021; 1416-14260006-3363CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://academic.oup.com/biolreprod/advance-article/doi/10.1093/biolre/ioab174/6369341info:eu-repo/semantics/altIdentifier/doi/10.1093/biolre/ioab174info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:49:58Zoai:ri.conicet.gov.ar:11336/158083instacron: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:34982025-09-29 09:49:58.996CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Allele-specific expression analysis reveals conserved and unique features of preimplantation development in equine ICSI embryos
title Allele-specific expression analysis reveals conserved and unique features of preimplantation development in equine ICSI embryos
spellingShingle Allele-specific expression analysis reveals conserved and unique features of preimplantation development in equine ICSI embryos
Goszczynski, Daniel Estanislao
HORSE GENOME ACTIVATION
DOSAGE COMPENSATION
X-CHROMOSOME INACTIVATION
ALLELIC BIAS
ICSI
SEXUAL DIMORPHISM
GENE EXPRESSION
title_short Allele-specific expression analysis reveals conserved and unique features of preimplantation development in equine ICSI embryos
title_full Allele-specific expression analysis reveals conserved and unique features of preimplantation development in equine ICSI embryos
title_fullStr Allele-specific expression analysis reveals conserved and unique features of preimplantation development in equine ICSI embryos
title_full_unstemmed Allele-specific expression analysis reveals conserved and unique features of preimplantation development in equine ICSI embryos
title_sort Allele-specific expression analysis reveals conserved and unique features of preimplantation development in equine ICSI embryos
dc.creator.none.fl_str_mv Goszczynski, Daniel Estanislao
Tinetti, P. S.
Choi, Y. H.
Ross, Pablo Juan
Hinrichs, K.
author Goszczynski, Daniel Estanislao
author_facet Goszczynski, Daniel Estanislao
Tinetti, P. S.
Choi, Y. H.
Ross, Pablo Juan
Hinrichs, K.
author_role author
author2 Tinetti, P. S.
Choi, Y. H.
Ross, Pablo Juan
Hinrichs, K.
author2_role author
author
author
author
dc.subject.none.fl_str_mv HORSE GENOME ACTIVATION
DOSAGE COMPENSATION
X-CHROMOSOME INACTIVATION
ALLELIC BIAS
ICSI
SEXUAL DIMORPHISM
GENE EXPRESSION
topic HORSE GENOME ACTIVATION
DOSAGE COMPENSATION
X-CHROMOSOME INACTIVATION
ALLELIC BIAS
ICSI
SEXUAL DIMORPHISM
GENE EXPRESSION
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Embryonic genome activation and dosage compensation are major genetic events in early development. Combined analysis of single embryo RNA-seq data and parental genome sequencing was used to evaluate parental contributions to early development and investigate X-chromosome dynamics. In addition, we evaluated dimorphism in gene expression between male and female embryos. Evaluation of parent-specific gene expression revealed a minor increase in paternal expression at the 4-cell stage that increased at the 8-cell stage. We also detected eight genes with allelic expression bias that may have an important role in early development, notably NANOGNB. The main actor in X-chromosome inactivation, XIST, was significantly upregulated at the 8-cell, morula, and blastocyst stages in female embryos, with high expression at the latter. Sexual dimorphism in gene expression was identified at all stages, with strong representation of the X-chromosome in females from the 16-cell to the blastocyst stage. Female embryos showed biparental X-chromosome expression at all stages after the 4-cell stage, demonstrating the absence of imprinted X-inactivation at the embryo level. The analysis of gene dosage showed incomplete dosage compensation (0.5 < X:A < 1) in MII oocytes and embryos up to the 4-cell stage, an increase of the X:A ratio at the 16-cell and morula stages after genome activation, and a decrease of the X:A ratio at the blastocyst stage, which might be associated with the beginning of X-chromosome inactivation. This study represents the first critical analysis of parent- and sex-specific gene expression in early equine embryos produced in vitro.
Fil: Goszczynski, Daniel Estanislao. University of California at Davis; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico CONICET- La Plata. Instituto de Genética Veterinaria "Ing. Fernando Noel Dulout". Universidad Nacional de La Plata. Facultad de Ciencias Veterinarias. Instituto de Genética Veterinaria; Argentina
Fil: Tinetti, P. S.. Texas A&M University; Estados Unidos
Fil: Choi, Y. H.. Texas A&M University; Estados Unidos
Fil: Ross, Pablo Juan. University of California at Davis; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Hinrichs, K.. Texas A&M University; Estados Unidos
description Embryonic genome activation and dosage compensation are major genetic events in early development. Combined analysis of single embryo RNA-seq data and parental genome sequencing was used to evaluate parental contributions to early development and investigate X-chromosome dynamics. In addition, we evaluated dimorphism in gene expression between male and female embryos. Evaluation of parent-specific gene expression revealed a minor increase in paternal expression at the 4-cell stage that increased at the 8-cell stage. We also detected eight genes with allelic expression bias that may have an important role in early development, notably NANOGNB. The main actor in X-chromosome inactivation, XIST, was significantly upregulated at the 8-cell, morula, and blastocyst stages in female embryos, with high expression at the latter. Sexual dimorphism in gene expression was identified at all stages, with strong representation of the X-chromosome in females from the 16-cell to the blastocyst stage. Female embryos showed biparental X-chromosome expression at all stages after the 4-cell stage, demonstrating the absence of imprinted X-inactivation at the embryo level. The analysis of gene dosage showed incomplete dosage compensation (0.5 < X:A < 1) in MII oocytes and embryos up to the 4-cell stage, an increase of the X:A ratio at the 16-cell and morula stages after genome activation, and a decrease of the X:A ratio at the blastocyst stage, which might be associated with the beginning of X-chromosome inactivation. This study represents the first critical analysis of parent- and sex-specific gene expression in early equine embryos produced in vitro.
publishDate 2021
dc.date.none.fl_str_mv 2021-09
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/11336/158083
Goszczynski, Daniel Estanislao; Tinetti, P. S.; Choi, Y. H.; Ross, Pablo Juan; Hinrichs, K.; Allele-specific expression analysis reveals conserved and unique features of preimplantation development in equine ICSI embryos; Society for the Study of Reproduction; Biology of Reproduction; 105; 6; 9-2021; 1416-1426
0006-3363
CONICET Digital
CONICET
url http://hdl.handle.net/11336/158083
identifier_str_mv Goszczynski, Daniel Estanislao; Tinetti, P. S.; Choi, Y. H.; Ross, Pablo Juan; Hinrichs, K.; Allele-specific expression analysis reveals conserved and unique features of preimplantation development in equine ICSI embryos; Society for the Study of Reproduction; Biology of Reproduction; 105; 6; 9-2021; 1416-1426
0006-3363
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://academic.oup.com/biolreprod/advance-article/doi/10.1093/biolre/ioab174/6369341
info:eu-repo/semantics/altIdentifier/doi/10.1093/biolre/ioab174
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
application/pdf
dc.publisher.none.fl_str_mv Society for the Study of Reproduction
publisher.none.fl_str_mv Society for the Study of Reproduction
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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