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Regulation of zygotic gene activation by chromatin structure and epigenetic factors

After fertilization, the genomes derived from an oocyte and spermatozoon are in a transcriptionally silent state before becoming activated at a species-specific time. In mice, the initiation of transcription occurs at the mid-one-cell stage, which represents the start of the gene expression program....

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Detalles Bibliográficos
Autores principales: FUNAYA, Satoshi, AOKI, Fugaku
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Society for Reproduction and Development 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593087/
https://www.ncbi.nlm.nih.gov/pubmed/28579579
http://dx.doi.org/10.1262/jrd.2017-058
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author FUNAYA, Satoshi
AOKI, Fugaku
author_facet FUNAYA, Satoshi
AOKI, Fugaku
author_sort FUNAYA, Satoshi
collection PubMed
description After fertilization, the genomes derived from an oocyte and spermatozoon are in a transcriptionally silent state before becoming activated at a species-specific time. In mice, the initiation of transcription occurs at the mid-one-cell stage, which represents the start of the gene expression program. A recent RNA sequencing analysis revealed that the gene expression pattern of one-cell embryos is unique and changes dramatically at the two-cell stage. However, the mechanism regulating this alteration has not yet been elucidated. It has been shown that chromatin structure and epigenetic factors change dynamically between the one- and two-cell stages. In this article, we review the characteristics of transcription, chromatin structure, and epigenetic factors in one- and two-cell mouse embryos and discuss the involvement of chromatin structure and epigenetic factors in the alteration of transcription that occurs between these stages.
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spelling pubmed-55930872017-09-18 Regulation of zygotic gene activation by chromatin structure and epigenetic factors FUNAYA, Satoshi AOKI, Fugaku J Reprod Dev Review After fertilization, the genomes derived from an oocyte and spermatozoon are in a transcriptionally silent state before becoming activated at a species-specific time. In mice, the initiation of transcription occurs at the mid-one-cell stage, which represents the start of the gene expression program. A recent RNA sequencing analysis revealed that the gene expression pattern of one-cell embryos is unique and changes dramatically at the two-cell stage. However, the mechanism regulating this alteration has not yet been elucidated. It has been shown that chromatin structure and epigenetic factors change dynamically between the one- and two-cell stages. In this article, we review the characteristics of transcription, chromatin structure, and epigenetic factors in one- and two-cell mouse embryos and discuss the involvement of chromatin structure and epigenetic factors in the alteration of transcription that occurs between these stages. The Society for Reproduction and Development 2017-06-03 2017-08 /pmc/articles/PMC5593087/ /pubmed/28579579 http://dx.doi.org/10.1262/jrd.2017-058 Text en ©2017 Society for Reproduction and Development This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Review
FUNAYA, Satoshi
AOKI, Fugaku
Regulation of zygotic gene activation by chromatin structure and epigenetic factors
title Regulation of zygotic gene activation by chromatin structure and epigenetic factors
title_full Regulation of zygotic gene activation by chromatin structure and epigenetic factors
title_fullStr Regulation of zygotic gene activation by chromatin structure and epigenetic factors
title_full_unstemmed Regulation of zygotic gene activation by chromatin structure and epigenetic factors
title_short Regulation of zygotic gene activation by chromatin structure and epigenetic factors
title_sort regulation of zygotic gene activation by chromatin structure and epigenetic factors
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593087/
https://www.ncbi.nlm.nih.gov/pubmed/28579579
http://dx.doi.org/10.1262/jrd.2017-058
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