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DNA polymerase α interacts with H3-H4 and facilitates the transfer of parental histones to lagging strands
How parental histones, the carriers of epigenetic modifications, are deposited onto replicating DNA remains poorly understood. Here, we describe the eSPAN method (enrichment and sequencing of protein-associated nascent DNA) in mouse embryonic stem (ES) cells and use it to detect histone deposition o...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7449674/ https://www.ncbi.nlm.nih.gov/pubmed/32923642 http://dx.doi.org/10.1126/sciadv.abb5820 |
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author | Li, Zhiming Hua, Xu Serra-Cardona, Albert Xu, Xiaowei Gan, Songlin Zhou, Hui Yang, Wen-Si Chen, Chun-long Xu, Rui-Ming Zhang, Zhiguo |
author_facet | Li, Zhiming Hua, Xu Serra-Cardona, Albert Xu, Xiaowei Gan, Songlin Zhou, Hui Yang, Wen-Si Chen, Chun-long Xu, Rui-Ming Zhang, Zhiguo |
author_sort | Li, Zhiming |
collection | PubMed |
description | How parental histones, the carriers of epigenetic modifications, are deposited onto replicating DNA remains poorly understood. Here, we describe the eSPAN method (enrichment and sequencing of protein-associated nascent DNA) in mouse embryonic stem (ES) cells and use it to detect histone deposition onto replicating DNA strands with a relatively small number of cells. We show that DNA polymerase α (Pol α), which synthesizes short primers for DNA synthesis, binds histone H3-H4 preferentially. A Pol α mutant defective in histone binding in vitro impairs the transfer of parental H3-H4 to lagging strands in both yeast and mouse ES cells. Last, dysregulation of both coding genes and noncoding endogenous retroviruses is detected in mutant ES cells defective in parental histone transfer. Together, we report an efficient eSPAN method for analysis of DNA replication–linked processes in mouse ES cells and reveal the mechanism of Pol α in parental histone transfer. |
format | Online Article Text |
id | pubmed-7449674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-74496742020-09-11 DNA polymerase α interacts with H3-H4 and facilitates the transfer of parental histones to lagging strands Li, Zhiming Hua, Xu Serra-Cardona, Albert Xu, Xiaowei Gan, Songlin Zhou, Hui Yang, Wen-Si Chen, Chun-long Xu, Rui-Ming Zhang, Zhiguo Sci Adv Research Articles How parental histones, the carriers of epigenetic modifications, are deposited onto replicating DNA remains poorly understood. Here, we describe the eSPAN method (enrichment and sequencing of protein-associated nascent DNA) in mouse embryonic stem (ES) cells and use it to detect histone deposition onto replicating DNA strands with a relatively small number of cells. We show that DNA polymerase α (Pol α), which synthesizes short primers for DNA synthesis, binds histone H3-H4 preferentially. A Pol α mutant defective in histone binding in vitro impairs the transfer of parental H3-H4 to lagging strands in both yeast and mouse ES cells. Last, dysregulation of both coding genes and noncoding endogenous retroviruses is detected in mutant ES cells defective in parental histone transfer. Together, we report an efficient eSPAN method for analysis of DNA replication–linked processes in mouse ES cells and reveal the mechanism of Pol α in parental histone transfer. American Association for the Advancement of Science 2020-08-26 /pmc/articles/PMC7449674/ /pubmed/32923642 http://dx.doi.org/10.1126/sciadv.abb5820 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Li, Zhiming Hua, Xu Serra-Cardona, Albert Xu, Xiaowei Gan, Songlin Zhou, Hui Yang, Wen-Si Chen, Chun-long Xu, Rui-Ming Zhang, Zhiguo DNA polymerase α interacts with H3-H4 and facilitates the transfer of parental histones to lagging strands |
title | DNA polymerase α interacts with H3-H4 and facilitates the transfer of parental histones to lagging strands |
title_full | DNA polymerase α interacts with H3-H4 and facilitates the transfer of parental histones to lagging strands |
title_fullStr | DNA polymerase α interacts with H3-H4 and facilitates the transfer of parental histones to lagging strands |
title_full_unstemmed | DNA polymerase α interacts with H3-H4 and facilitates the transfer of parental histones to lagging strands |
title_short | DNA polymerase α interacts with H3-H4 and facilitates the transfer of parental histones to lagging strands |
title_sort | dna polymerase α interacts with h3-h4 and facilitates the transfer of parental histones to lagging strands |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7449674/ https://www.ncbi.nlm.nih.gov/pubmed/32923642 http://dx.doi.org/10.1126/sciadv.abb5820 |
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