Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans

Recurrent spontaneous abortion (RSA) is a common cause of infertility, but previous attempts at identifying RSA causative genes have been relatively unsuccessful. Such failure to describe RSA aetiological genes might be explained by the fact that reproductive phenotypes should be considered as quant...

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Autores:
Tipo de recurso:
Fecha de publicación:
2016
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/21963
Acceso en línea:
https://doi.org/10.1098/rsob.160109
https://repository.urosario.edu.co/handle/10336/21963
Palabra clave:
Evolución & genética
Ginecología & otras especialidades médicas
Developmental biology
Genetics
Genomics
FOXD1 protein
Embryo death
Recurrent spontaneous abortion
Interspecific recombinant congenic mice
DNA microarray
Forkhead transcription factor
Chlorocebus aethiops
C57BL mouse
CV-1 cell line
Rights
License
Abierto (Texto Completo)
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oai_identifier_str oai:repository.urosario.edu.co:10336/21963
network_acronym_str EDOCUR2
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repository_id_str
dc.title.spa.fl_str_mv Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans
title Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans
spellingShingle Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans
Evolución & genética
Ginecología & otras especialidades médicas
Developmental biology
Genetics
Genomics
FOXD1 protein
Embryo death
Recurrent spontaneous abortion
Interspecific recombinant congenic mice
DNA microarray
Forkhead transcription factor
Chlorocebus aethiops
C57BL mouse
CV-1 cell line
title_short Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans
title_full Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans
title_fullStr Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans
title_full_unstemmed Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans
title_sort Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans
dc.subject.ddc.spa.fl_str_mv Evolución & genética
Ginecología & otras especialidades médicas
topic Evolución & genética
Ginecología & otras especialidades médicas
Developmental biology
Genetics
Genomics
FOXD1 protein
Embryo death
Recurrent spontaneous abortion
Interspecific recombinant congenic mice
DNA microarray
Forkhead transcription factor
Chlorocebus aethiops
C57BL mouse
CV-1 cell line
dc.subject.keyword.spa.fl_str_mv Developmental biology
Genetics
Genomics
FOXD1 protein
Embryo death
Recurrent spontaneous abortion
Interspecific recombinant congenic mice
DNA microarray
Forkhead transcription factor
Chlorocebus aethiops
C57BL mouse
CV-1 cell line
description Recurrent spontaneous abortion (RSA) is a common cause of infertility, but previous attempts at identifying RSA causative genes have been relatively unsuccessful. Such failure to describe RSA aetiological genes might be explained by the fact that reproductive phenotypes should be considered as quantitative traits resulting from the intricate interaction of numerous genetic, epigenetic and environmental factors. Here, we studied an interspecific recombinant congenic strain (IRCS) of Mus musculus from the C57BL6/J strain of mice harbouring an approximate 5 Mb DNA fragment from chromosome 13 from Mus spretus mice (66H-MMU13 strain), with a high rate of embryonic resorption (ER). Transcriptome analyses of endometrial and placental tissues from these mice showed a deregulation of many genes associated with the coagulation and inflammatory response pathways. Bioinformatics approaches led us to select Foxd1 as a candidate gene potentially related to ER and RSA. Sequencing analysis of Foxd1 in the 66H-MMU13 strain, and in 556 women affected by RSA and 271 controls revealed non-synonymous sequence variants. In vitro assays revealed that some led to perturbations in FOXD1 transactivation properties on promoters of genes having key roles during implantation/placentation, suggesting a role of this gene in mammalian implantation processes. © 2016 The Authors.
publishDate 2016
dc.date.created.none.fl_str_mv 2016-10-01
dc.date.issued.none.fl_str_mv 2016
dc.date.accessioned.none.fl_str_mv 2020-05-12T00:22:30Z
dc.date.available.none.fl_str_mv 2020-05-12T00:22:30Z
dc.type.eng.fl_str_mv article
dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.coar.fl_str_mv http://purl.org/coar/resource_type/c_6501
dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1098/rsob.160109
dc.identifier.issn.none.fl_str_mv 2046-2441
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/21963
url https://doi.org/10.1098/rsob.160109
https://repository.urosario.edu.co/handle/10336/21963
identifier_str_mv 2046-2441
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationIssue.none.fl_str_mv No. 10
dc.relation.citationTitle.none.fl_str_mv Open biology
dc.relation.citationVolume.none.fl_str_mv Vol. 6
dc.relation.ispartof.spa.fl_str_mv Open biology, ISSN: 2046-2441 Vol. 6, No. 10 (Septiembre 2016); 13 pp.
dc.relation.uri.spa.fl_str_mv https://royalsocietypublishing.org/doi/10.1098/rsob.160109
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institution Universidad del Rosario
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dc.source.reponame.none.fl_str_mv reponame:Repositorio Institucional EdocUR
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spelling 7978277060013d26a6f-0fb5-4e62-9bac-7dda0221bf3c600196c31ed-c46c-4cc7-9455-7a3f30d448be60088556bf3-6f30-4d7f-a7c2-ef57eaf554bd600e25a6e77-c935-4581-9685-a82a589af5926008641dbbb-db7e-4786-9685-229ba16950a660038531971-4d0c-401a-a536-e31139669f3c600cf38c850-8bfd-45db-ba50-02f6d3ff3778600f522fd44-dc61-46de-bd5e-12fa58e25203600117e3fc6-ba19-4674-a294-35f244bb13f1600615fb687-62e1-4144-bb3a-2adaab3be144600d8bf62ee-00a4-4aaa-a59a-8427acc60f1560034f3b8e0-0fca-45c9-8e17-0784a98d734960064824866-9c7d-41a7-85bf-1e3f4f61e67460092db8eae-5c21-462f-8472-a03490645880600f28d10b9-5542-4581-813f-9c55fbd801fe6006c92e4d5-791e-4d4e-b620-0ccf615a0a4d6008c04e2c5-11d7-4123-9d4a-5dff54e26fd7600060cd606-a1b2-4ff3-8204-0b5b56af77506002020-05-12T00:22:30Z2020-05-12T00:22:30Z2016-10-012016Recurrent spontaneous abortion (RSA) is a common cause of infertility, but previous attempts at identifying RSA causative genes have been relatively unsuccessful. Such failure to describe RSA aetiological genes might be explained by the fact that reproductive phenotypes should be considered as quantitative traits resulting from the intricate interaction of numerous genetic, epigenetic and environmental factors. Here, we studied an interspecific recombinant congenic strain (IRCS) of Mus musculus from the C57BL6/J strain of mice harbouring an approximate 5 Mb DNA fragment from chromosome 13 from Mus spretus mice (66H-MMU13 strain), with a high rate of embryonic resorption (ER). Transcriptome analyses of endometrial and placental tissues from these mice showed a deregulation of many genes associated with the coagulation and inflammatory response pathways. Bioinformatics approaches led us to select Foxd1 as a candidate gene potentially related to ER and RSA. Sequencing analysis of Foxd1 in the 66H-MMU13 strain, and in 556 women affected by RSA and 271 controls revealed non-synonymous sequence variants. In vitro assays revealed that some led to perturbations in FOXD1 transactivation properties on promoters of genes having key roles during implantation/placentation, suggesting a role of this gene in mammalian implantation processes. © 2016 The Authors.application/pdfhttps://doi.org/10.1098/rsob.1601092046-2441https://repository.urosario.edu.co/handle/10336/21963engNo. 10Open biologyVol. 6Open biology, ISSN: 2046-2441 Vol. 6, No. 10 (Septiembre 2016); 13 pp.https://royalsocietypublishing.org/doi/10.1098/rsob.160109Abierto (Texto Completo)http://purl.org/coar/access_right/c_abf2instname:Universidad del Rosarioreponame:Repositorio Institucional EdocUREvolución & genética575600Ginecología & otras especialidades médicas618600Developmental biologyGeneticsGenomicsFOXD1 proteinEmbryo deathRecurrent spontaneous abortionInterspecific recombinant congenic miceDNA microarrayForkhead transcription factorChlorocebus aethiopsC57BL mouseCV-1 cell lineAssociation of FOXD1 variants with adverse pregnancy outcomes in mice and humansarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Laissue, PaulLakha, BesmaVatin, MagalieBatista, FrankBurgio, GaetanMercier, EricDos Santos, EstherBuffat, ChristopheSierra Diaz, Diana CarolinaRenault, GillesMontagutelli, XavierSalmon, JaneMonget, PhilippeVeitia, ReinerMeháts, CélineFellous, MarcGris, Jean-ChristopheCocquet, JulieVaiman, DanielLaissue, P.Lakhal, B.Vatin, M.Batista, F.Burgio, G.Mercier, E.Santos, E.D.Buffat, C.Sierra-Diaz, D.C.Renault, G.Montagutelli, X.Salmon, J.Monget, P.Veitia, R.A.Méhats, C.Fellous, M.Gris, J.-C.Cocquet, J.Vaiman, D.ORIGINALAssociation_of_FOXD1_variants_with_adverse_pregnancy_outcomes_in_mice_and_humans.pdfapplication/pdf1170689https://repository.urosario.edu.co/bitstreams/a5abf7b0-b74b-4aa6-9a57-b6b81ab58199/download898e2dfd76462314935be67a13bfe037MD51TEXTAssociation_of_FOXD1_variants_with_adverse_pregnancy_outcomes_in_mice_and_humans.pdf.txtAssociation_of_FOXD1_variants_with_adverse_pregnancy_outcomes_in_mice_and_humans.pdf.txtExtracted texttext/plain67406https://repository.urosario.edu.co/bitstreams/a65a018e-f932-4138-8813-a2b379d68bf2/downloadcac50adf1fe0c0222ece0d29e3f5f9f0MD52THUMBNAILAssociation_of_FOXD1_variants_with_adverse_pregnancy_outcomes_in_mice_and_humans.pdf.jpgAssociation_of_FOXD1_variants_with_adverse_pregnancy_outcomes_in_mice_and_humans.pdf.jpgGenerated Thumbnailimage/jpeg4702https://repository.urosario.edu.co/bitstreams/679b3a37-43dd-4d22-a625-7a69f0f725e3/download2345fcab82b8d26c44e0bb768866d89aMD5310336/21963oai:repository.urosario.edu.co:10336/219632020-05-13 14:49:50.23https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co