Non-meiotic chromosome instability in human immature oocytes
Aneuploidy has been a major issue in human gametes and is closely related to fertility problems, as it is known to be present in cleavage stage embryos and gestational losses. Pre-meiotic chromosome abnormalities in women have been previously described. The aim of this study is to assess the whole-c...
| Autores: | , , , , , , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2014 |
| País: | España |
| Institución: | Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau) |
| Repositorio: | r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau |
| OAI Identifier: | oai:iibsantpau.fundanetsuite.com:p9017 |
| Acceso en línea: | https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=9017 |
| Access Level: | acceso abierto |
| Palabra clave: | premeiotic instability immature oocytes aneuploidy segmental imbalances germline mitotic abnormalities |
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Non-meiotic chromosome instability in human immature oocytesDaina, GRamos, LRius, MObradors, Adel Rey, JGiralt, MCampillo, MVelilla, EPujol, AMartinez-Pasarell, OBenet, FNavarro, Jpremeiotic instabilityimmature oocytesaneuploidysegmental imbalancesgermline mitotic abnormalitiesAneuploidy has been a major issue in human gametes and is closely related to fertility problems, as it is known to be present in cleavage stage embryos and gestational losses. Pre-meiotic chromosome abnormalities in women have been previously described. The aim of this study is to assess the whole-chromosome complement in immature oocytes to find those abnormalities caused by mitotic instability. For this purpose, a total of 157 oocytes at the germinal vesicle or metaphase I stage, and discarded from IVF cycles, were analysed by CGH. Fifty-six women, between 18 and 45 years old (mean 32.5 years), including 32 IVF patients (25-45 years of age) and 24 IVF oocyte donors (18-33 years of age), were included in the study. A total of 25/157 (15.9%) of the oocytes analysed, obtained from three IVF clinics, contained chromosome abnormalities, including both aneuploidy (24/157) and structural aberrations (9/157). Independently of the maternal age, the incidence of abnormal oocytes which originated before meiosis is 15.9%, and these imbalances were found in 33.9% of the females studied. This work sheds light on the relevance of mitotic instability responsible for the generation of the abnormalities present in human oocytes.NATURE PUBLISHING GROUP2014info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttps://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=9017EUROPEAN JOURNAL OF HUMAN GENETICSISSN: 10184813ISSNe: 14765438reponame:r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pauinstname:Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau)Inglésinfo:eu-repo/semantics/openAccessoai:iibsantpau.fundanetsuite.com:p90172026-06-14T12:41:47Z |
| dc.title.none.fl_str_mv |
Non-meiotic chromosome instability in human immature oocytes |
| title |
Non-meiotic chromosome instability in human immature oocytes |
| spellingShingle |
Non-meiotic chromosome instability in human immature oocytes Daina, G premeiotic instability immature oocytes aneuploidy segmental imbalances germline mitotic abnormalities |
| title_short |
Non-meiotic chromosome instability in human immature oocytes |
| title_full |
Non-meiotic chromosome instability in human immature oocytes |
| title_fullStr |
Non-meiotic chromosome instability in human immature oocytes |
| title_full_unstemmed |
Non-meiotic chromosome instability in human immature oocytes |
| title_sort |
Non-meiotic chromosome instability in human immature oocytes |
| dc.creator.none.fl_str_mv |
Daina, G Ramos, L Rius, M Obradors, A del Rey, J Giralt, M Campillo, M Velilla, E Pujol, A Martinez-Pasarell, O Benet, F Navarro, J |
| author |
Daina, G |
| author_facet |
Daina, G Ramos, L Rius, M Obradors, A del Rey, J Giralt, M Campillo, M Velilla, E Pujol, A Martinez-Pasarell, O Benet, F Navarro, J |
| author_role |
author |
| author2 |
Ramos, L Rius, M Obradors, A del Rey, J Giralt, M Campillo, M Velilla, E Pujol, A Martinez-Pasarell, O Benet, F Navarro, J |
| author2_role |
author author author author author author author author author author author |
| dc.subject.none.fl_str_mv |
premeiotic instability immature oocytes aneuploidy segmental imbalances germline mitotic abnormalities |
| topic |
premeiotic instability immature oocytes aneuploidy segmental imbalances germline mitotic abnormalities |
| description |
Aneuploidy has been a major issue in human gametes and is closely related to fertility problems, as it is known to be present in cleavage stage embryos and gestational losses. Pre-meiotic chromosome abnormalities in women have been previously described. The aim of this study is to assess the whole-chromosome complement in immature oocytes to find those abnormalities caused by mitotic instability. For this purpose, a total of 157 oocytes at the germinal vesicle or metaphase I stage, and discarded from IVF cycles, were analysed by CGH. Fifty-six women, between 18 and 45 years old (mean 32.5 years), including 32 IVF patients (25-45 years of age) and 24 IVF oocyte donors (18-33 years of age), were included in the study. A total of 25/157 (15.9%) of the oocytes analysed, obtained from three IVF clinics, contained chromosome abnormalities, including both aneuploidy (24/157) and structural aberrations (9/157). Independently of the maternal age, the incidence of abnormal oocytes which originated before meiosis is 15.9%, and these imbalances were found in 33.9% of the females studied. This work sheds light on the relevance of mitotic instability responsible for the generation of the abnormalities present in human oocytes. |
| publishDate |
2014 |
| dc.date.none.fl_str_mv |
2014 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=9017 |
| url |
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=9017 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess |
| eu_rights_str_mv |
openAccess |
| dc.publisher.none.fl_str_mv |
NATURE PUBLISHING GROUP |
| publisher.none.fl_str_mv |
NATURE PUBLISHING GROUP |
| dc.source.none.fl_str_mv |
EUROPEAN JOURNAL OF HUMAN GENETICS ISSN: 10184813 ISSNe: 14765438 reponame:r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau instname:Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau) |
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Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau) |
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r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau |
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r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau |
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15,811543 |