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Chromosomal coordination and differential structure of asynchronous replicating regions
Stochastic asynchronous replication timing (AS-RT) is a phenomenon in which the time of replication of each allele is different, and the identity of the early allele varies between cells. By taking advantage of stable clonal pre-B cell populations derived from C57BL6/Castaneous mice, we have mapped...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884787/ https://www.ncbi.nlm.nih.gov/pubmed/33589603 http://dx.doi.org/10.1038/s41467-021-21348-4 |
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author | Blumenfeld, Britny Masika, Hagit Farago, Marganit Yehuda, Yishai Halaseh, Lamia Vardi, Oriya Rapoport, Rachel Levin-Klein, Rena Cedar, Howard Bergman, Yehudit Simon, Itamar |
author_facet | Blumenfeld, Britny Masika, Hagit Farago, Marganit Yehuda, Yishai Halaseh, Lamia Vardi, Oriya Rapoport, Rachel Levin-Klein, Rena Cedar, Howard Bergman, Yehudit Simon, Itamar |
author_sort | Blumenfeld, Britny |
collection | PubMed |
description | Stochastic asynchronous replication timing (AS-RT) is a phenomenon in which the time of replication of each allele is different, and the identity of the early allele varies between cells. By taking advantage of stable clonal pre-B cell populations derived from C57BL6/Castaneous mice, we have mapped the genome-wide AS-RT loci, independently of genetic differences. These regions are characterized by differential chromatin accessibility, mono-allelic expression and include new gene families involved in specifying cell identity. By combining population level mapping with single cell FISH, our data reveal the existence of a novel regulatory program that coordinates a fixed relationship between AS-RT regions on any given chromosome, with some loci set to replicate in a parallel and others set in the anti-parallel orientation. Our results show that AS-RT is a highly regulated epigenetic mark established during early embryogenesis that may be used for facilitating the programming of mono-allelic choice throughout development. |
format | Online Article Text |
id | pubmed-7884787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78847872021-03-03 Chromosomal coordination and differential structure of asynchronous replicating regions Blumenfeld, Britny Masika, Hagit Farago, Marganit Yehuda, Yishai Halaseh, Lamia Vardi, Oriya Rapoport, Rachel Levin-Klein, Rena Cedar, Howard Bergman, Yehudit Simon, Itamar Nat Commun Article Stochastic asynchronous replication timing (AS-RT) is a phenomenon in which the time of replication of each allele is different, and the identity of the early allele varies between cells. By taking advantage of stable clonal pre-B cell populations derived from C57BL6/Castaneous mice, we have mapped the genome-wide AS-RT loci, independently of genetic differences. These regions are characterized by differential chromatin accessibility, mono-allelic expression and include new gene families involved in specifying cell identity. By combining population level mapping with single cell FISH, our data reveal the existence of a novel regulatory program that coordinates a fixed relationship between AS-RT regions on any given chromosome, with some loci set to replicate in a parallel and others set in the anti-parallel orientation. Our results show that AS-RT is a highly regulated epigenetic mark established during early embryogenesis that may be used for facilitating the programming of mono-allelic choice throughout development. Nature Publishing Group UK 2021-02-15 /pmc/articles/PMC7884787/ /pubmed/33589603 http://dx.doi.org/10.1038/s41467-021-21348-4 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Blumenfeld, Britny Masika, Hagit Farago, Marganit Yehuda, Yishai Halaseh, Lamia Vardi, Oriya Rapoport, Rachel Levin-Klein, Rena Cedar, Howard Bergman, Yehudit Simon, Itamar Chromosomal coordination and differential structure of asynchronous replicating regions |
title | Chromosomal coordination and differential structure of asynchronous replicating regions |
title_full | Chromosomal coordination and differential structure of asynchronous replicating regions |
title_fullStr | Chromosomal coordination and differential structure of asynchronous replicating regions |
title_full_unstemmed | Chromosomal coordination and differential structure of asynchronous replicating regions |
title_short | Chromosomal coordination and differential structure of asynchronous replicating regions |
title_sort | chromosomal coordination and differential structure of asynchronous replicating regions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884787/ https://www.ncbi.nlm.nih.gov/pubmed/33589603 http://dx.doi.org/10.1038/s41467-021-21348-4 |
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