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Epigenetic Modifications during Angiosperm Gametogenesis

Angiosperms do not contain a distinct germline, but rather develop gametes from gametophyte initials that undergo cell division. These gametes contain cells that give rise to an endosperm and the embryo. DNA methylation is decreased in the vegetative nucleus (VN) and central cell nuclei (CCN) result...

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Detalles Bibliográficos
Autores principales: Migicovsky, Zoë, Kovalchuk, Igor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3355800/
https://www.ncbi.nlm.nih.gov/pubmed/22645573
http://dx.doi.org/10.3389/fpls.2012.00020
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author Migicovsky, Zoë
Kovalchuk, Igor
author_facet Migicovsky, Zoë
Kovalchuk, Igor
author_sort Migicovsky, Zoë
collection PubMed
description Angiosperms do not contain a distinct germline, but rather develop gametes from gametophyte initials that undergo cell division. These gametes contain cells that give rise to an endosperm and the embryo. DNA methylation is decreased in the vegetative nucleus (VN) and central cell nuclei (CCN) resulting in expression of transposable elements (TEs). It is thought that the siRNAs produced in response to TE expression are able to travel to the sperm cells and egg cells (EC) from VN and CCN, respectively, in order to enforce silencing there. Demethylation during gametogenesis helps ensure that even newly integrated TEs are expressed and therefore silenced by the resulting siRNA production. A final form of epigenetic control is modification of histones, which includes accumulation of the H3 variant HTR10 in mature sperm that is then completely replaced following fertilization. In females, the histone isoforms present in the EC and CCN differ, potentially helping to differentiate the two components during gametogenesis.
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spelling pubmed-33558002012-05-29 Epigenetic Modifications during Angiosperm Gametogenesis Migicovsky, Zoë Kovalchuk, Igor Front Plant Sci Plant Science Angiosperms do not contain a distinct germline, but rather develop gametes from gametophyte initials that undergo cell division. These gametes contain cells that give rise to an endosperm and the embryo. DNA methylation is decreased in the vegetative nucleus (VN) and central cell nuclei (CCN) resulting in expression of transposable elements (TEs). It is thought that the siRNAs produced in response to TE expression are able to travel to the sperm cells and egg cells (EC) from VN and CCN, respectively, in order to enforce silencing there. Demethylation during gametogenesis helps ensure that even newly integrated TEs are expressed and therefore silenced by the resulting siRNA production. A final form of epigenetic control is modification of histones, which includes accumulation of the H3 variant HTR10 in mature sperm that is then completely replaced following fertilization. In females, the histone isoforms present in the EC and CCN differ, potentially helping to differentiate the two components during gametogenesis. Frontiers Research Foundation 2012-02-06 /pmc/articles/PMC3355800/ /pubmed/22645573 http://dx.doi.org/10.3389/fpls.2012.00020 Text en Copyright © 2012 Migicovsky and Kovalchuk. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
spellingShingle Plant Science
Migicovsky, Zoë
Kovalchuk, Igor
Epigenetic Modifications during Angiosperm Gametogenesis
title Epigenetic Modifications during Angiosperm Gametogenesis
title_full Epigenetic Modifications during Angiosperm Gametogenesis
title_fullStr Epigenetic Modifications during Angiosperm Gametogenesis
title_full_unstemmed Epigenetic Modifications during Angiosperm Gametogenesis
title_short Epigenetic Modifications during Angiosperm Gametogenesis
title_sort epigenetic modifications during angiosperm gametogenesis
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3355800/
https://www.ncbi.nlm.nih.gov/pubmed/22645573
http://dx.doi.org/10.3389/fpls.2012.00020
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