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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Main Authors: Mitsutoshi Yamada, Dieter Egli
Format: Article
Language:English
Published: Elsevier 2017-03-01
Series:Stem Cell Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S221367111730036X
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spelling 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
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AT dieteregli genometransferpreventsfragmentationandrestoresdevelopmentalpotentialofdevelopmentallycompromisedpostovulatoryagedmouseoocytes
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