YY1’s role in the Peg3 imprinted domain

Abstract The ICR (Imprinting Control Region) of the Peg3 (Paternally Expressed Gene 3) domain contains an unusual cluster of YY1 binding sites. In the current study, these YY1 binding sites were mutated to characterize the unknown roles in the mouse Peg3 domain. According to the results, paternal an...

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Autores principales: Hongzhi He, An Ye, Bambarendage P. U. Perera, Joomyeong Kim
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/aae8f4d347f64f8a9dcf9bb197d0dc36
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spelling oai:doaj.org-article:aae8f4d347f64f8a9dcf9bb197d0dc362021-12-02T16:07:46ZYY1’s role in the Peg3 imprinted domain10.1038/s41598-017-06817-52045-2322https://doaj.org/article/aae8f4d347f64f8a9dcf9bb197d0dc362017-07-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-06817-5https://doaj.org/toc/2045-2322Abstract The ICR (Imprinting Control Region) of the Peg3 (Paternally Expressed Gene 3) domain contains an unusual cluster of YY1 binding sites. In the current study, these YY1 binding sites were mutated to characterize the unknown roles in the mouse Peg3 domain. According to the results, paternal and maternal transmission of the mutant allele did not cause any major effect on the survival of the pups. In the mutants, the maternal-specific DNA methylation on the ICR was properly established and maintained, causing no major effect on the imprinting of the domain. In contrast, the paternal transmission resulted in changes in the expression levels of several genes: down-regulation of Peg3 and Usp29 and up-regulation of Zim1. These changes were more pronounced during the neonatal stage than during the adult stage. In the case of Peg3 and Zim1, the levels of the observed changes were also different between males and females, suggesting the different degrees of YY1 involvement between two sexes. Overall, the results indicated that YY1 is mainly involved in controlling the transcriptional levels, but not the DNA methylation, of the Peg3 domain.Hongzhi HeAn YeBambarendage P. U. PereraJoomyeong KimNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-11 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Hongzhi He
An Ye
Bambarendage P. U. Perera
Joomyeong Kim
YY1’s role in the Peg3 imprinted domain
description Abstract The ICR (Imprinting Control Region) of the Peg3 (Paternally Expressed Gene 3) domain contains an unusual cluster of YY1 binding sites. In the current study, these YY1 binding sites were mutated to characterize the unknown roles in the mouse Peg3 domain. According to the results, paternal and maternal transmission of the mutant allele did not cause any major effect on the survival of the pups. In the mutants, the maternal-specific DNA methylation on the ICR was properly established and maintained, causing no major effect on the imprinting of the domain. In contrast, the paternal transmission resulted in changes in the expression levels of several genes: down-regulation of Peg3 and Usp29 and up-regulation of Zim1. These changes were more pronounced during the neonatal stage than during the adult stage. In the case of Peg3 and Zim1, the levels of the observed changes were also different between males and females, suggesting the different degrees of YY1 involvement between two sexes. Overall, the results indicated that YY1 is mainly involved in controlling the transcriptional levels, but not the DNA methylation, of the Peg3 domain.
format article
author Hongzhi He
An Ye
Bambarendage P. U. Perera
Joomyeong Kim
author_facet Hongzhi He
An Ye
Bambarendage P. U. Perera
Joomyeong Kim
author_sort Hongzhi He
title YY1’s role in the Peg3 imprinted domain
title_short YY1’s role in the Peg3 imprinted domain
title_full YY1’s role in the Peg3 imprinted domain
title_fullStr YY1’s role in the Peg3 imprinted domain
title_full_unstemmed YY1’s role in the Peg3 imprinted domain
title_sort yy1’s role in the peg3 imprinted domain
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/aae8f4d347f64f8a9dcf9bb197d0dc36
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