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Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR

BACKGROUND: Zrsr1 is a paternally expressed imprinted gene located in the first intron of Commd1, and the Zrsr1 promoter resides in a differentially methylated region (DMR) that is maternally methylated in the oocyte. However, a mechanism for the establishment of the methylation has remained obscure...

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Autores principales: Joh, Keiichiro, Matsuhisa, Fumikazu, Kitajima, Shuji, Nishioka, Kenichi, Higashimoto, Ken, Yatsuki, Hitomi, Kono, Tomohiro, Koseki, Haruhiko, Soejima, Hidenobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989421/
https://www.ncbi.nlm.nih.gov/pubmed/29875017
http://dx.doi.org/10.1186/s13072-018-0200-6
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author Joh, Keiichiro
Matsuhisa, Fumikazu
Kitajima, Shuji
Nishioka, Kenichi
Higashimoto, Ken
Yatsuki, Hitomi
Kono, Tomohiro
Koseki, Haruhiko
Soejima, Hidenobu
author_facet Joh, Keiichiro
Matsuhisa, Fumikazu
Kitajima, Shuji
Nishioka, Kenichi
Higashimoto, Ken
Yatsuki, Hitomi
Kono, Tomohiro
Koseki, Haruhiko
Soejima, Hidenobu
author_sort Joh, Keiichiro
collection PubMed
description BACKGROUND: Zrsr1 is a paternally expressed imprinted gene located in the first intron of Commd1, and the Zrsr1 promoter resides in a differentially methylated region (DMR) that is maternally methylated in the oocyte. However, a mechanism for the establishment of the methylation has remained obscure. Commd1 is transcribed in the opposite direction to Zrsr1 with predominant maternal expression, especially in the adult brain. RESULTS: We found Commed1 transcribed through the DMR in the growing oocyte. Zrsr1-DMR methylation was abolished by the prevention of Commd1 transcription. Furthermore, methylation did not occur at the artificially unmethylated maternal Zrsr1-DMR during embryonic development when transcription through the DMR was restored in the zygote. Loss of methylation at the maternal Zrsr1-DMR resulted in biallelic Zrsr1 expression and reduced the extent of the predominant maternal expression of Commd1. CONCLUSIONS: These results indicate that the establishment of methylation at Zrsr1-DMR occurs in a transcription-dependent and oocyte-specific manner and caused Zrsr1 imprinting by repressing maternal expression. The predominant maternal expression of Commd1 is likely caused by transcriptional interference by paternal Zrsr1 expression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13072-018-0200-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-59894212018-06-20 Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR Joh, Keiichiro Matsuhisa, Fumikazu Kitajima, Shuji Nishioka, Kenichi Higashimoto, Ken Yatsuki, Hitomi Kono, Tomohiro Koseki, Haruhiko Soejima, Hidenobu Epigenetics Chromatin Research BACKGROUND: Zrsr1 is a paternally expressed imprinted gene located in the first intron of Commd1, and the Zrsr1 promoter resides in a differentially methylated region (DMR) that is maternally methylated in the oocyte. However, a mechanism for the establishment of the methylation has remained obscure. Commd1 is transcribed in the opposite direction to Zrsr1 with predominant maternal expression, especially in the adult brain. RESULTS: We found Commed1 transcribed through the DMR in the growing oocyte. Zrsr1-DMR methylation was abolished by the prevention of Commd1 transcription. Furthermore, methylation did not occur at the artificially unmethylated maternal Zrsr1-DMR during embryonic development when transcription through the DMR was restored in the zygote. Loss of methylation at the maternal Zrsr1-DMR resulted in biallelic Zrsr1 expression and reduced the extent of the predominant maternal expression of Commd1. CONCLUSIONS: These results indicate that the establishment of methylation at Zrsr1-DMR occurs in a transcription-dependent and oocyte-specific manner and caused Zrsr1 imprinting by repressing maternal expression. The predominant maternal expression of Commd1 is likely caused by transcriptional interference by paternal Zrsr1 expression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13072-018-0200-6) contains supplementary material, which is available to authorized users. BioMed Central 2018-06-06 /pmc/articles/PMC5989421/ /pubmed/29875017 http://dx.doi.org/10.1186/s13072-018-0200-6 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Joh, Keiichiro
Matsuhisa, Fumikazu
Kitajima, Shuji
Nishioka, Kenichi
Higashimoto, Ken
Yatsuki, Hitomi
Kono, Tomohiro
Koseki, Haruhiko
Soejima, Hidenobu
Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR
title Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR
title_full Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR
title_fullStr Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR
title_full_unstemmed Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR
title_short Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR
title_sort growing oocyte-specific transcription-dependent de novo dna methylation at the imprinted zrsr1-dmr
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989421/
https://www.ncbi.nlm.nih.gov/pubmed/29875017
http://dx.doi.org/10.1186/s13072-018-0200-6
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