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Landscape transcriptomic analysis of bovine follicular cells during key phases of ovarian follicular development

dc.contributor.authorMogollón García, Henry David [UNESP]
dc.contributor.authorde Andrade Ferrazza, Rodrigo
dc.contributor.authorOchoa, Julian Camilo [UNESP]
dc.contributor.authorde Athayde, Flávia Florencio [UNESP]
dc.contributor.authorVidigal, Pedro Marcus Pereira
dc.contributor.authorWiltbank, Milo
dc.contributor.authorKastelic, John Patrick
dc.contributor.authorSartori, Roberto
dc.contributor.authorFerreira, João Carlos Pinheiro [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual de Londrina (UEL)
dc.contributor.institutionViçosa Federal University
dc.contributor.institutionUniversity of Wisconsin-Madison
dc.contributor.institutionUniversity of Calgary
dc.date.accessioned2025-04-29T18:41:37Z
dc.date.issued2024-12-01
dc.description.abstractBackground: There are many gaps in our understanding of the mechanisms involved in ovarian follicular development in cattle, particularly regarding follicular deviation, acquisition of ovulatory capacity, and preovulatory changes. Molecular evaluations of ovarian follicular cells during follicular development in cattle, especially serial transcriptomic analyses across key growth phases, have not been reported. This study aims to address this gap by analyzing gene expression using RNA-seq in granulosa and antral cells recovered from ovarian follicular fluid during critical phases of ovarian follicular development in Holstein cows. Results: Integrated analysis of gene ontology (GO), gene set enrichment (GSEA), protein–protein interaction (PPI), and gene topology identified that differentially expressed genes (DEGs) in the largest ovarian follicles at deviation (Dev) were primarily involved in FSH-negative feedback, steroidogenesis, cell proliferation, apoptosis, and the prevention of early follicle rupture. In contrast, DEGs in the second largest follicles (DevF2) were mainly related to loss of cell viability, apoptosis, and immune cell invasion. In the dominant (PostDev) and preovulatory (PreOv) follicles, DEGs were associated with vascular changes and inflammatory responses. Conclusions: The transcriptome of ovarian follicular fluid cells had a predominance of granulosa cells in the dominant follicle at deviation, with upregulation of genes involved in cell viability, steroidogenesis, and apoptosis prevention, whereas in the non-selected follicle there was upregulation of cell death-related transcripts. Immune cell transcripts increased significantly after deviation, particularly in preovulatory follicles, indicating strong intrafollicular chemotactic activity. We inferred that immune cell invasion occurred despite an intact basal lamina, contributing to follicular maturation. Graphical Abstract: (Figure presented.)en
dc.description.affiliationDepartment of Veterinary Surgery and Animal Reproduction School of Veterinary Medicine and Animal Science São Paulo State University (UNESP), Rua Prof. Doutor Walter Mauricio Correa, s/n, São Paulo
dc.description.affiliationDepartment of Genetic Evolution Microbiology and Immunology. Biology Institute Campinas State University, São Paulo
dc.description.affiliationComputational Systems Biology Laboratory (CSBL) Institut Pasteur University of São Paulo (USP)
dc.description.affiliationDepartment of Animal Science Londrina State University, Paraná
dc.description.affiliationDepartment of Animal Production and Health School of Veterinary Medicine São Paulo State University (UNESP), São Paulo
dc.description.affiliationCenter of Biological Sciences Viçosa Federal University, Minas Gerais
dc.description.affiliationDepartment of Animal & Dairy Sciences University of Wisconsin-Madison
dc.description.affiliationFaculty of Veterinary Medicine University of Calgary
dc.description.affiliationDepartment of Animal Science Luiz de Queiroz College of Agriculture (ESALQ) University of São Paulo, São Paulo
dc.description.affiliationUnespDepartment of Veterinary Surgery and Animal Reproduction School of Veterinary Medicine and Animal Science São Paulo State University (UNESP), Rua Prof. Doutor Walter Mauricio Correa, s/n, São Paulo
dc.description.affiliationUnespDepartment of Animal Production and Health School of Veterinary Medicine São Paulo State University (UNESP), São Paulo
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdCNPq: 190043/2017-2
dc.description.sponsorshipIdFAPESP: 2011/20449-7
dc.description.sponsorshipIdFAPESP: 2012/18297-7
dc.identifierhttp://dx.doi.org/10.1186/s40659-024-00558-2
dc.identifier.citationBiological Research, v. 57, n. 1, 2024.
dc.identifier.doi10.1186/s40659-024-00558-2
dc.identifier.issn0717-6287
dc.identifier.issn0716-9760
dc.identifier.scopus2-s2.0-85207815620
dc.identifier.urihttps://hdl.handle.net/11449/299186
dc.language.isoeng
dc.relation.ispartofBiological Research
dc.sourceScopus
dc.subjectDeviation
dc.subjectGenes
dc.subjectHolstein cows
dc.subjectSteroidogenesis
dc.titleLandscape transcriptomic analysis of bovine follicular cells during key phases of ovarian follicular developmenten
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication1f8041b8-563c-4766-90b9-4dd9c0101666
relation.isOrgUnitOfPublication9ca5a87b-0c83-43fa-b290-6f8a4202bf99
relation.isOrgUnitOfPublication.latestForDiscovery1f8041b8-563c-4766-90b9-4dd9c0101666
unesp.author.orcid0000-0002-7742-8254[9]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina Veterinária e Zootecnia, Botucatupt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina Veterinária, Araçatubapt

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