Genome Transfer Prevents Fragmentation and Restores Developmental Potential of Developmentally Compromised Postovulatory Aged Mouse Oocytes
Changes in oocyte quality can have great impact on the developmental potential of early embryos. Here we test whether nuclear genome transfer from a developmentally incompetent to a developmentally competent oocyte can restore developmental potential. Using in vitro oocyte aging as a model system we...
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doaj-196ae073f4de40b897d654a3993eb6072020-11-24T23:51:57ZengElsevierStem Cell Reports2213-67112017-03-018357658810.1016/j.stemcr.2017.01.020Genome Transfer Prevents Fragmentation and Restores Developmental Potential of Developmentally Compromised Postovulatory Aged Mouse OocytesMitsutoshi Yamada0Dieter Egli1The New York Stem Cell Foundation Research Institute, New York, NY 10032, USAThe New York Stem Cell Foundation Research Institute, New York, NY 10032, USAChanges in oocyte quality can have great impact on the developmental potential of early embryos. Here we test whether nuclear genome transfer from a developmentally incompetent to a developmentally competent oocyte can restore developmental potential. Using in vitro oocyte aging as a model system we performed nuclear transfer in mouse oocytes at metaphase II or at the first interphase, and observed that development to the blastocyst stage and to term was as efficient as in control embryos. The increased developmental potential is explained primarily by correction of abnormal cytokinesis at anaphase of meiosis and mitosis, by a reduction in chromosome segregation errors, and by normalization of the localization of chromosome passenger complex components survivin and cyclin B1. These observations demonstrate that developmental decline is primarily due to abnormal function of cytoplasmic factors involved in cytokinesis, while the genome remains developmentally fully competent.http://www.sciencedirect.com/science/article/pii/S221367111730036Xgenome exchangeoocyte agingmousefragmentation |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mitsutoshi Yamada Dieter Egli |
spellingShingle |
Mitsutoshi Yamada Dieter Egli Genome Transfer Prevents Fragmentation and Restores Developmental Potential of Developmentally Compromised Postovulatory Aged Mouse Oocytes Stem Cell Reports genome exchange oocyte aging mouse fragmentation |
author_facet |
Mitsutoshi Yamada Dieter Egli |
author_sort |
Mitsutoshi Yamada |
title |
Genome Transfer Prevents Fragmentation and Restores Developmental Potential of Developmentally Compromised Postovulatory Aged Mouse Oocytes |
title_short |
Genome Transfer Prevents Fragmentation and Restores Developmental Potential of Developmentally Compromised Postovulatory Aged Mouse Oocytes |
title_full |
Genome Transfer Prevents Fragmentation and Restores Developmental Potential of Developmentally Compromised Postovulatory Aged Mouse Oocytes |
title_fullStr |
Genome Transfer Prevents Fragmentation and Restores Developmental Potential of Developmentally Compromised Postovulatory Aged Mouse Oocytes |
title_full_unstemmed |
Genome Transfer Prevents Fragmentation and Restores Developmental Potential of Developmentally Compromised Postovulatory Aged Mouse Oocytes |
title_sort |
genome transfer prevents fragmentation and restores developmental potential of developmentally compromised postovulatory aged mouse oocytes |
publisher |
Elsevier |
series |
Stem Cell Reports |
issn |
2213-6711 |
publishDate |
2017-03-01 |
description |
Changes in oocyte quality can have great impact on the developmental potential of early embryos. Here we test whether nuclear genome transfer from a developmentally incompetent to a developmentally competent oocyte can restore developmental potential. Using in vitro oocyte aging as a model system we performed nuclear transfer in mouse oocytes at metaphase II or at the first interphase, and observed that development to the blastocyst stage and to term was as efficient as in control embryos. The increased developmental potential is explained primarily by correction of abnormal cytokinesis at anaphase of meiosis and mitosis, by a reduction in chromosome segregation errors, and by normalization of the localization of chromosome passenger complex components survivin and cyclin B1. These observations demonstrate that developmental decline is primarily due to abnormal function of cytoplasmic factors involved in cytokinesis, while the genome remains developmentally fully competent. |
topic |
genome exchange oocyte aging mouse fragmentation |
url |
http://www.sciencedirect.com/science/article/pii/S221367111730036X |
work_keys_str_mv |
AT mitsutoshiyamada genometransferpreventsfragmentationandrestoresdevelopmentalpotentialofdevelopmentallycompromisedpostovulatoryagedmouseoocytes AT dieteregli genometransferpreventsfragmentationandrestoresdevelopmentalpotentialofdevelopmentallycompromisedpostovulatoryagedmouseoocytes |
_version_ |
1725475385645203456 |