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Regulation of Mouse Retroelement MuERV-L/MERVL Expression by REX1 and Epigenetic Control of Stem Cell Potency

About half of the mammalian genome is occupied by DNA sequences that originate from transposable elements. Retrotransposons can modulate gene expression in different ways and, particularly retrotransposon-derived long terminal repeats, profoundly shape expression of both surrounding and distant geno...

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Autores principales: Schoorlemmer, Jon, Pérez-Palacios, Raquel, Climent, María, Guallar, Diana, Muniesa, Pedro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3915180/
https://www.ncbi.nlm.nih.gov/pubmed/24567914
http://dx.doi.org/10.3389/fonc.2014.00014
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author Schoorlemmer, Jon
Pérez-Palacios, Raquel
Climent, María
Guallar, Diana
Muniesa, Pedro
author_facet Schoorlemmer, Jon
Pérez-Palacios, Raquel
Climent, María
Guallar, Diana
Muniesa, Pedro
author_sort Schoorlemmer, Jon
collection PubMed
description About half of the mammalian genome is occupied by DNA sequences that originate from transposable elements. Retrotransposons can modulate gene expression in different ways and, particularly retrotransposon-derived long terminal repeats, profoundly shape expression of both surrounding and distant genomic loci. This is especially important in pre-implantation development, during which extensive reprograming of the genome takes place and cells pass through totipotent and pluripotent states. At this stage, the main mechanism responsible for retrotransposon silencing, i.e., DNA methylation, is inoperative. A particular retrotransposon called muERV-L/MERVL is expressed during pre-implantation stages and contributes to the plasticity of mouse embryonic stem cells. This review will focus on the role of MERVL-derived sequences as controlling elements of gene expression specific for pre-implantation development, two-cell stage-specific gene expression, and stem cell pluripotency, the epigenetic mechanisms that control their expression, and the contributions of the pluripotency marker REX1 and the related Yin Yang 1 family of transcription factors to this regulation process.
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spelling pubmed-39151802014-02-24 Regulation of Mouse Retroelement MuERV-L/MERVL Expression by REX1 and Epigenetic Control of Stem Cell Potency Schoorlemmer, Jon Pérez-Palacios, Raquel Climent, María Guallar, Diana Muniesa, Pedro Front Oncol Oncology About half of the mammalian genome is occupied by DNA sequences that originate from transposable elements. Retrotransposons can modulate gene expression in different ways and, particularly retrotransposon-derived long terminal repeats, profoundly shape expression of both surrounding and distant genomic loci. This is especially important in pre-implantation development, during which extensive reprograming of the genome takes place and cells pass through totipotent and pluripotent states. At this stage, the main mechanism responsible for retrotransposon silencing, i.e., DNA methylation, is inoperative. A particular retrotransposon called muERV-L/MERVL is expressed during pre-implantation stages and contributes to the plasticity of mouse embryonic stem cells. This review will focus on the role of MERVL-derived sequences as controlling elements of gene expression specific for pre-implantation development, two-cell stage-specific gene expression, and stem cell pluripotency, the epigenetic mechanisms that control their expression, and the contributions of the pluripotency marker REX1 and the related Yin Yang 1 family of transcription factors to this regulation process. Frontiers Media S.A. 2014-02-06 /pmc/articles/PMC3915180/ /pubmed/24567914 http://dx.doi.org/10.3389/fonc.2014.00014 Text en Copyright © 2014 Schoorlemmer, Pérez-Palacios, Climent, Guallar and Muniesa. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Schoorlemmer, Jon
Pérez-Palacios, Raquel
Climent, María
Guallar, Diana
Muniesa, Pedro
Regulation of Mouse Retroelement MuERV-L/MERVL Expression by REX1 and Epigenetic Control of Stem Cell Potency
title Regulation of Mouse Retroelement MuERV-L/MERVL Expression by REX1 and Epigenetic Control of Stem Cell Potency
title_full Regulation of Mouse Retroelement MuERV-L/MERVL Expression by REX1 and Epigenetic Control of Stem Cell Potency
title_fullStr Regulation of Mouse Retroelement MuERV-L/MERVL Expression by REX1 and Epigenetic Control of Stem Cell Potency
title_full_unstemmed Regulation of Mouse Retroelement MuERV-L/MERVL Expression by REX1 and Epigenetic Control of Stem Cell Potency
title_short Regulation of Mouse Retroelement MuERV-L/MERVL Expression by REX1 and Epigenetic Control of Stem Cell Potency
title_sort regulation of mouse retroelement muerv-l/mervl expression by rex1 and epigenetic control of stem cell potency
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3915180/
https://www.ncbi.nlm.nih.gov/pubmed/24567914
http://dx.doi.org/10.3389/fonc.2014.00014
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