Characterization of novel paternal ncRNAs at the Plagl1 locus, including Hymai, predicted to interact with regulators of active chromatin.

Genomic imprinting is a complex epigenetic mechanism of transcriptional control that utilizes DNA methylation and histone modifications to bring about parent-of-origin specific monoallelic expression in mammals. Genes subject to imprinting are often organised in clusters associated with large non-co...

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Main Authors: Isabel Iglesias-Platas, Alex Martin-Trujillo, Davide Cirillo, Franck Court, Amy Guillaumet-Adkins, Cristina Camprubi, Deborah Bourc'his, Kenichiro Hata, Robert Feil, Gian Tartaglia, Philippe Arnaud, David Monk
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0038907&type=printable
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author Isabel Iglesias-Platas
Alex Martin-Trujillo
Davide Cirillo
Franck Court
Amy Guillaumet-Adkins
Cristina Camprubi
Deborah Bourc'his
Kenichiro Hata
Robert Feil
Gian Tartaglia
Philippe Arnaud
David Monk
author_facet Isabel Iglesias-Platas
Alex Martin-Trujillo
Davide Cirillo
Franck Court
Amy Guillaumet-Adkins
Cristina Camprubi
Deborah Bourc'his
Kenichiro Hata
Robert Feil
Gian Tartaglia
Philippe Arnaud
David Monk
author_sort Isabel Iglesias-Platas
collection DOAJ
description Genomic imprinting is a complex epigenetic mechanism of transcriptional control that utilizes DNA methylation and histone modifications to bring about parent-of-origin specific monoallelic expression in mammals. Genes subject to imprinting are often organised in clusters associated with large non-coding RNAs (ncRNAs), some of which have cis-regulatory functions. Here we have undertaken a detailed allelic expression analysis of an imprinted domain on mouse proximal chromosome 10 comprising the paternally expressed Plagl1 gene. We identified three novel Plagl1 transcripts, only one of which contains protein-coding exons. In addition, we characterised two unspliced ncRNAs, Hymai, the mouse orthologue of HYMAI, and Plagl1it (Plagl1 intronic transcript), a transcript located in intron 5 of Plagl1. Imprinted expression of these novel ncRNAs requires DNMT3L-mediated maternal DNA methylation, which is also indispensable for establishing the correct chromatin profile at the Plagl1 DMR. Significantly, the two ncRNAs are retained in the nucleus, consistent with a potential regulatory function at the imprinted domain. Analysis with catRAPID, a protein-ncRNA association prediction algorithm, suggests that Hymai and Plagl1it RNAs both have potentially high affinity for Trithorax chromatin regulators. The two ncRNAs could therefore help to protect the paternal allele from DNA methylation by attracting Trithorax proteins that mediate H3 lysine-4 methylation.
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spelling doaj-art-75a973f630334971b059ce2ecb05af1d2025-08-20T02:30:51ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0176e3890710.1371/journal.pone.0038907Characterization of novel paternal ncRNAs at the Plagl1 locus, including Hymai, predicted to interact with regulators of active chromatin.Isabel Iglesias-PlatasAlex Martin-TrujilloDavide CirilloFranck CourtAmy Guillaumet-AdkinsCristina CamprubiDeborah Bourc'hisKenichiro HataRobert FeilGian TartagliaPhilippe ArnaudDavid MonkGenomic imprinting is a complex epigenetic mechanism of transcriptional control that utilizes DNA methylation and histone modifications to bring about parent-of-origin specific monoallelic expression in mammals. Genes subject to imprinting are often organised in clusters associated with large non-coding RNAs (ncRNAs), some of which have cis-regulatory functions. Here we have undertaken a detailed allelic expression analysis of an imprinted domain on mouse proximal chromosome 10 comprising the paternally expressed Plagl1 gene. We identified three novel Plagl1 transcripts, only one of which contains protein-coding exons. In addition, we characterised two unspliced ncRNAs, Hymai, the mouse orthologue of HYMAI, and Plagl1it (Plagl1 intronic transcript), a transcript located in intron 5 of Plagl1. Imprinted expression of these novel ncRNAs requires DNMT3L-mediated maternal DNA methylation, which is also indispensable for establishing the correct chromatin profile at the Plagl1 DMR. Significantly, the two ncRNAs are retained in the nucleus, consistent with a potential regulatory function at the imprinted domain. Analysis with catRAPID, a protein-ncRNA association prediction algorithm, suggests that Hymai and Plagl1it RNAs both have potentially high affinity for Trithorax chromatin regulators. The two ncRNAs could therefore help to protect the paternal allele from DNA methylation by attracting Trithorax proteins that mediate H3 lysine-4 methylation.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0038907&type=printable
spellingShingle Isabel Iglesias-Platas
Alex Martin-Trujillo
Davide Cirillo
Franck Court
Amy Guillaumet-Adkins
Cristina Camprubi
Deborah Bourc'his
Kenichiro Hata
Robert Feil
Gian Tartaglia
Philippe Arnaud
David Monk
Characterization of novel paternal ncRNAs at the Plagl1 locus, including Hymai, predicted to interact with regulators of active chromatin.
PLoS ONE
title Characterization of novel paternal ncRNAs at the Plagl1 locus, including Hymai, predicted to interact with regulators of active chromatin.
title_full Characterization of novel paternal ncRNAs at the Plagl1 locus, including Hymai, predicted to interact with regulators of active chromatin.
title_fullStr Characterization of novel paternal ncRNAs at the Plagl1 locus, including Hymai, predicted to interact with regulators of active chromatin.
title_full_unstemmed Characterization of novel paternal ncRNAs at the Plagl1 locus, including Hymai, predicted to interact with regulators of active chromatin.
title_short Characterization of novel paternal ncRNAs at the Plagl1 locus, including Hymai, predicted to interact with regulators of active chromatin.
title_sort characterization of novel paternal ncrnas at the plagl1 locus including hymai predicted to interact with regulators of active chromatin
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0038907&type=printable
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