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Cohesin in Oocytes—Tough Enough for Mammalian Meiosis?

Sister chromatid cohesion is essential for cell division. During meiosis, it is also required for proper synapsis of pairs of sister chromatids and for chiasma formation and maintenance. Since mammalian oocytes remain arrested in late prophase for a very long period—up to five decades in humans—the...

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Detalles Bibliográficos
Autores principales: Revenkova, Ekaterina, Adelfalk, Caroline, Jessberger, Rolf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3966221/
https://www.ncbi.nlm.nih.gov/pubmed/24710099
http://dx.doi.org/10.3390/genes1030495
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author Revenkova, Ekaterina
Adelfalk, Caroline
Jessberger, Rolf
author_facet Revenkova, Ekaterina
Adelfalk, Caroline
Jessberger, Rolf
author_sort Revenkova, Ekaterina
collection PubMed
description Sister chromatid cohesion is essential for cell division. During meiosis, it is also required for proper synapsis of pairs of sister chromatids and for chiasma formation and maintenance. Since mammalian oocytes remain arrested in late prophase for a very long period—up to five decades in humans—the preservation of cohesion throughout this period is a formidable challenge. Mouse models with cohesin deficiencies and aging wild-type mice showed that this challenge is not fully met: cohesion weakens and deteriorates with increasing age. These recent findings have highly significant implications for our comprehension of the genesis of aneuploidies.
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spelling pubmed-39662212014-03-26 Cohesin in Oocytes—Tough Enough for Mammalian Meiosis? Revenkova, Ekaterina Adelfalk, Caroline Jessberger, Rolf Genes (Basel) Review Sister chromatid cohesion is essential for cell division. During meiosis, it is also required for proper synapsis of pairs of sister chromatids and for chiasma formation and maintenance. Since mammalian oocytes remain arrested in late prophase for a very long period—up to five decades in humans—the preservation of cohesion throughout this period is a formidable challenge. Mouse models with cohesin deficiencies and aging wild-type mice showed that this challenge is not fully met: cohesion weakens and deteriorates with increasing age. These recent findings have highly significant implications for our comprehension of the genesis of aneuploidies. MDPI 2010-12-13 /pmc/articles/PMC3966221/ /pubmed/24710099 http://dx.doi.org/10.3390/genes1030495 Text en © 2010 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Revenkova, Ekaterina
Adelfalk, Caroline
Jessberger, Rolf
Cohesin in Oocytes—Tough Enough for Mammalian Meiosis?
title Cohesin in Oocytes—Tough Enough for Mammalian Meiosis?
title_full Cohesin in Oocytes—Tough Enough for Mammalian Meiosis?
title_fullStr Cohesin in Oocytes—Tough Enough for Mammalian Meiosis?
title_full_unstemmed Cohesin in Oocytes—Tough Enough for Mammalian Meiosis?
title_short Cohesin in Oocytes—Tough Enough for Mammalian Meiosis?
title_sort cohesin in oocytes—tough enough for mammalian meiosis?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3966221/
https://www.ncbi.nlm.nih.gov/pubmed/24710099
http://dx.doi.org/10.3390/genes1030495
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