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DNA Replication Timing Enters the Single-Cell Era

In mammalian cells, DNA replication timing is controlled at the level of megabase (Mb)-sized chromosomal domains and correlates well with transcription, chromatin structure, and three-dimensional (3D) genome organization. Because of these properties, DNA replication timing is an excellent entry poin...

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Autores principales: Hiratani, Ichiro, Takahashi, Saori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470765/
https://www.ncbi.nlm.nih.gov/pubmed/30884743
http://dx.doi.org/10.3390/genes10030221
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author Hiratani, Ichiro
Takahashi, Saori
author_facet Hiratani, Ichiro
Takahashi, Saori
author_sort Hiratani, Ichiro
collection PubMed
description In mammalian cells, DNA replication timing is controlled at the level of megabase (Mb)-sized chromosomal domains and correlates well with transcription, chromatin structure, and three-dimensional (3D) genome organization. Because of these properties, DNA replication timing is an excellent entry point to explore genome regulation at various levels and a variety of studies have been carried out over the years. However, DNA replication timing studies traditionally required at least tens of thousands of cells, and it was unclear whether the replication domains detected by cell population analyses were preserved at the single-cell level. Recently, single-cell DNA replication profiling methods became available, which revealed that the Mb-sized replication domains detected by cell population analyses were actually well preserved in individual cells. In this article, we provide a brief overview of our current knowledge on DNA replication timing regulation in mammals based on cell population studies, outline the findings from single-cell DNA replication profiling, and discuss future directions and challenges.
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spelling pubmed-64707652019-04-27 DNA Replication Timing Enters the Single-Cell Era Hiratani, Ichiro Takahashi, Saori Genes (Basel) Review In mammalian cells, DNA replication timing is controlled at the level of megabase (Mb)-sized chromosomal domains and correlates well with transcription, chromatin structure, and three-dimensional (3D) genome organization. Because of these properties, DNA replication timing is an excellent entry point to explore genome regulation at various levels and a variety of studies have been carried out over the years. However, DNA replication timing studies traditionally required at least tens of thousands of cells, and it was unclear whether the replication domains detected by cell population analyses were preserved at the single-cell level. Recently, single-cell DNA replication profiling methods became available, which revealed that the Mb-sized replication domains detected by cell population analyses were actually well preserved in individual cells. In this article, we provide a brief overview of our current knowledge on DNA replication timing regulation in mammals based on cell population studies, outline the findings from single-cell DNA replication profiling, and discuss future directions and challenges. MDPI 2019-03-15 /pmc/articles/PMC6470765/ /pubmed/30884743 http://dx.doi.org/10.3390/genes10030221 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Hiratani, Ichiro
Takahashi, Saori
DNA Replication Timing Enters the Single-Cell Era
title DNA Replication Timing Enters the Single-Cell Era
title_full DNA Replication Timing Enters the Single-Cell Era
title_fullStr DNA Replication Timing Enters the Single-Cell Era
title_full_unstemmed DNA Replication Timing Enters the Single-Cell Era
title_short DNA Replication Timing Enters the Single-Cell Era
title_sort dna replication timing enters the single-cell era
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470765/
https://www.ncbi.nlm.nih.gov/pubmed/30884743
http://dx.doi.org/10.3390/genes10030221
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