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Asynchronous Replication Timing: A Mechanism for Monoallelic Choice During Development
Developmental programming is carried out by a sequence of molecular choices that epigenetically mark the genome to generate the stable cell types which make up the total organism. A number of important processes, such as genomic imprinting, selection of immune or olfactory receptors, and X-chromosom...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8517340/ https://www.ncbi.nlm.nih.gov/pubmed/34660595 http://dx.doi.org/10.3389/fcell.2021.737681 |
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author | Bergman, Yehudit Simon, Itamar Cedar, Howard |
author_facet | Bergman, Yehudit Simon, Itamar Cedar, Howard |
author_sort | Bergman, Yehudit |
collection | PubMed |
description | Developmental programming is carried out by a sequence of molecular choices that epigenetically mark the genome to generate the stable cell types which make up the total organism. A number of important processes, such as genomic imprinting, selection of immune or olfactory receptors, and X-chromosome inactivation in females are dependent on the ability to stably choose one single allele in each cell. In this perspective, we propose that asynchronous replication timing (ASRT) serves as the basis for a sophisticated universal mechanism for mediating and maintaining these decisions. |
format | Online Article Text |
id | pubmed-8517340 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85173402021-10-16 Asynchronous Replication Timing: A Mechanism for Monoallelic Choice During Development Bergman, Yehudit Simon, Itamar Cedar, Howard Front Cell Dev Biol Cell and Developmental Biology Developmental programming is carried out by a sequence of molecular choices that epigenetically mark the genome to generate the stable cell types which make up the total organism. A number of important processes, such as genomic imprinting, selection of immune or olfactory receptors, and X-chromosome inactivation in females are dependent on the ability to stably choose one single allele in each cell. In this perspective, we propose that asynchronous replication timing (ASRT) serves as the basis for a sophisticated universal mechanism for mediating and maintaining these decisions. Frontiers Media S.A. 2021-10-01 /pmc/articles/PMC8517340/ /pubmed/34660595 http://dx.doi.org/10.3389/fcell.2021.737681 Text en Copyright © 2021 Bergman, Simon and Cedar. https://creativecommons.org/licenses/by/4.0/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) and the copyright owner(s) 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 | Cell and Developmental Biology Bergman, Yehudit Simon, Itamar Cedar, Howard Asynchronous Replication Timing: A Mechanism for Monoallelic Choice During Development |
title | Asynchronous Replication Timing: A Mechanism for Monoallelic Choice During Development |
title_full | Asynchronous Replication Timing: A Mechanism for Monoallelic Choice During Development |
title_fullStr | Asynchronous Replication Timing: A Mechanism for Monoallelic Choice During Development |
title_full_unstemmed | Asynchronous Replication Timing: A Mechanism for Monoallelic Choice During Development |
title_short | Asynchronous Replication Timing: A Mechanism for Monoallelic Choice During Development |
title_sort | asynchronous replication timing: a mechanism for monoallelic choice during development |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8517340/ https://www.ncbi.nlm.nih.gov/pubmed/34660595 http://dx.doi.org/10.3389/fcell.2021.737681 |
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