Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Zhiming, Hua, Xu, Serra-Cardona, Albert, Xu, Xiaowei, Gan, Songlin, Zhou, Hui, Yang, Wen-Si, Chen, Chun-long, Xu, Rui-Ming, Zhang, Zhiguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
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
_version_ 1783574674037276672
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
work_keys_str_mv AT lizhiming dnapolymeraseainteractswithh3h4andfacilitatesthetransferofparentalhistonestolaggingstrands
AT huaxu dnapolymeraseainteractswithh3h4andfacilitatesthetransferofparentalhistonestolaggingstrands
AT serracardonaalbert dnapolymeraseainteractswithh3h4andfacilitatesthetransferofparentalhistonestolaggingstrands
AT xuxiaowei dnapolymeraseainteractswithh3h4andfacilitatesthetransferofparentalhistonestolaggingstrands
AT gansonglin dnapolymeraseainteractswithh3h4andfacilitatesthetransferofparentalhistonestolaggingstrands
AT zhouhui dnapolymeraseainteractswithh3h4andfacilitatesthetransferofparentalhistonestolaggingstrands
AT yangwensi dnapolymeraseainteractswithh3h4andfacilitatesthetransferofparentalhistonestolaggingstrands
AT chenchunlong dnapolymeraseainteractswithh3h4andfacilitatesthetransferofparentalhistonestolaggingstrands
AT xuruiming dnapolymeraseainteractswithh3h4andfacilitatesthetransferofparentalhistonestolaggingstrands
AT zhangzhiguo dnapolymeraseainteractswithh3h4andfacilitatesthetransferofparentalhistonestolaggingstrands