The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing

Primary ovarian insufficiency (POI) is a frequently occurring pathology, leading to infertility. Genetic anomalies have been described in POI and mutations in numerous genes have been definitively related to the pathogenesis of the disease. Some studies based on next generation sequencing (NGS) have...

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Tipo de recurso:
Fecha de publicación:
2018
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/22605
Acceso en línea:
https://doi.org/10.1016/j.mce.2017.07.021
https://repository.urosario.edu.co/handle/10336/22605
Palabra clave:
Gene expression
Gene mutation
Human
Massively parallel sequencing
Meiosis
Next generation sequencing
Nonhuman
Ovary follicle development
Ovulation
Pathogenesis
Premature ovarian failure
Priority journal
Review
Sequence analysis
Sex determination
Female
Genetics
High throughput sequencing
Metabolism
Ovary follicle
Premature ovarian failure
Procedures
Sex determination process
Female
High-throughput nucleotide sequencing
Humans
Meiosis
Ovarian follicle
Ovulation
Primary ovarian insufficiency
Sex determination processes
Female infertility
Molecular aetiology
Next generation sequencing
Primary ovarian insufficiency
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spelling f27097fd-56db-4d27-91ed-7ffc57f6a046-12020-05-25T23:57:06Z2020-05-25T23:57:06Z2018Primary ovarian insufficiency (POI) is a frequently occurring pathology, leading to infertility. Genetic anomalies have been described in POI and mutations in numerous genes have been definitively related to the pathogenesis of the disease. Some studies based on next generation sequencing (NGS) have been successfully undertaken as they have led to identify new mutations associated with POI aetiology. The purpose of this review is to present the most relevant molecules involved in diverse complex pathways, which may contribute towards POI. The main genes participating in bipotential gonad formation, sex determination, meiosis, folliculogenesis and ovulation are described to enable understanding how they may be considered putative candidates involved in POI. Considerations regarding NGS technical aspects such as design and data interpretation are mentioned. Successful NGS initiatives used for POI studying and future challenges are also discussed. © 2017 Elsevier B.V.application/pdfhttps://doi.org/10.1016/j.mce.2017.07.0213037207https://repository.urosario.edu.co/handle/10336/22605engElsevier Ireland Ltd180170Molecular and Cellular EndocrinologyVol. 460Molecular and Cellular Endocrinology, ISSN:3037207, Vol.460,(2018); pp. 170-180https://www.scopus.com/inward/record.uri?eid=2-s2.0-85025838278&doi=10.1016%2fj.mce.2017.07.021&partnerID=40&md5=279ced63f83ca6e682a36982b5fda24cAbierto (Texto Completo)http://purl.org/coar/access_right/c_abf2instname:Universidad del Rosarioreponame:Repositorio Institucional EdocURGene expressionGene mutationHumanMassively parallel sequencingMeiosisNext generation sequencingNonhumanOvary follicle developmentOvulationPathogenesisPremature ovarian failurePriority journalReviewSequence analysisSex determinationFemaleGeneticsHigh throughput sequencingMetabolismOvary folliclePremature ovarian failureProceduresSex determination processFemaleHigh-throughput nucleotide sequencingHumansMeiosisOvarian follicleOvulationPrimary ovarian insufficiencySex determination processesFemale infertilityMolecular aetiologyNext generation sequencingPrimary ovarian insufficiencyThe molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencingarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Laissue P.ORIGINAL1-s2-0-S0303720717303945-main.pdfapplication/pdf387692https://repository.urosario.edu.co/bitstreams/972fea9b-d7de-437f-aa40-b218386d499c/download0e16da5a587ee305a7e202903256247aMD51TEXT1-s2-0-S0303720717303945-main.pdf.txt1-s2-0-S0303720717303945-main.pdf.txtExtracted texttext/plain91190https://repository.urosario.edu.co/bitstreams/d711bbd0-51d8-44ba-9c96-fd1ed79dfdc7/download780e17cedcee739a674b0b70e9d21bc4MD52THUMBNAIL1-s2-0-S0303720717303945-main.pdf.jpg1-s2-0-S0303720717303945-main.pdf.jpgGenerated Thumbnailimage/jpeg4414https://repository.urosario.edu.co/bitstreams/4b0feacc-70a6-412e-9ba6-515fe6e82eb9/download8b63d7050eef581a60ba9ad8986e5dc5MD5310336/22605oai:repository.urosario.edu.co:10336/226052022-05-02 07:37:20.558081https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co
dc.title.spa.fl_str_mv The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing
title The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing
spellingShingle The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing
Gene expression
Gene mutation
Human
Massively parallel sequencing
Meiosis
Next generation sequencing
Nonhuman
Ovary follicle development
Ovulation
Pathogenesis
Premature ovarian failure
Priority journal
Review
Sequence analysis
Sex determination
Female
Genetics
High throughput sequencing
Metabolism
Ovary follicle
Premature ovarian failure
Procedures
Sex determination process
Female
High-throughput nucleotide sequencing
Humans
Meiosis
Ovarian follicle
Ovulation
Primary ovarian insufficiency
Sex determination processes
Female infertility
Molecular aetiology
Next generation sequencing
Primary ovarian insufficiency
title_short The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing
title_full The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing
title_fullStr The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing
title_full_unstemmed The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing
title_sort The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing
dc.subject.keyword.spa.fl_str_mv Gene expression
Gene mutation
Human
Massively parallel sequencing
Meiosis
Next generation sequencing
Nonhuman
Ovary follicle development
Ovulation
Pathogenesis
Premature ovarian failure
Priority journal
Review
Sequence analysis
Sex determination
Female
Genetics
High throughput sequencing
Metabolism
Ovary follicle
Premature ovarian failure
Procedures
Sex determination process
Female
High-throughput nucleotide sequencing
Humans
Meiosis
Ovarian follicle
Ovulation
Primary ovarian insufficiency
Sex determination processes
Female infertility
Molecular aetiology
Next generation sequencing
Primary ovarian insufficiency
topic Gene expression
Gene mutation
Human
Massively parallel sequencing
Meiosis
Next generation sequencing
Nonhuman
Ovary follicle development
Ovulation
Pathogenesis
Premature ovarian failure
Priority journal
Review
Sequence analysis
Sex determination
Female
Genetics
High throughput sequencing
Metabolism
Ovary follicle
Premature ovarian failure
Procedures
Sex determination process
Female
High-throughput nucleotide sequencing
Humans
Meiosis
Ovarian follicle
Ovulation
Primary ovarian insufficiency
Sex determination processes
Female infertility
Molecular aetiology
Next generation sequencing
Primary ovarian insufficiency
description Primary ovarian insufficiency (POI) is a frequently occurring pathology, leading to infertility. Genetic anomalies have been described in POI and mutations in numerous genes have been definitively related to the pathogenesis of the disease. Some studies based on next generation sequencing (NGS) have been successfully undertaken as they have led to identify new mutations associated with POI aetiology. The purpose of this review is to present the most relevant molecules involved in diverse complex pathways, which may contribute towards POI. The main genes participating in bipotential gonad formation, sex determination, meiosis, folliculogenesis and ovulation are described to enable understanding how they may be considered putative candidates involved in POI. Considerations regarding NGS technical aspects such as design and data interpretation are mentioned. Successful NGS initiatives used for POI studying and future challenges are also discussed. © 2017 Elsevier B.V.
publishDate 2018
dc.date.created.spa.fl_str_mv 2018
dc.date.accessioned.none.fl_str_mv 2020-05-25T23:57:06Z
dc.date.available.none.fl_str_mv 2020-05-25T23:57:06Z
dc.type.eng.fl_str_mv article
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dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1016/j.mce.2017.07.021
dc.identifier.issn.none.fl_str_mv 3037207
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/22605
url https://doi.org/10.1016/j.mce.2017.07.021
https://repository.urosario.edu.co/handle/10336/22605
identifier_str_mv 3037207
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationEndPage.none.fl_str_mv 180
dc.relation.citationStartPage.none.fl_str_mv 170
dc.relation.citationTitle.none.fl_str_mv Molecular and Cellular Endocrinology
dc.relation.citationVolume.none.fl_str_mv Vol. 460
dc.relation.ispartof.spa.fl_str_mv Molecular and Cellular Endocrinology, ISSN:3037207, Vol.460,(2018); pp. 170-180
dc.relation.uri.spa.fl_str_mv https://www.scopus.com/inward/record.uri?eid=2-s2.0-85025838278&doi=10.1016%2fj.mce.2017.07.021&partnerID=40&md5=279ced63f83ca6e682a36982b5fda24c
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rights_invalid_str_mv Abierto (Texto Completo)
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dc.publisher.spa.fl_str_mv Elsevier Ireland Ltd
institution Universidad del Rosario
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