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Asymmetric histone inheritance via strand-specific incorporation and biased replication fork movement

Many stem cells undergo asymmetric division to produce a self-renewing stem cell and a differentiating daughter cell. Here we show that, similarly to H3, histone H4 is inherited asymmetrically in Drosophila melanogaster male germline stem cells undergoing asymmetric division. In contrast, both H2A a...

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Autores principales: Wooten, Matthew, Snedeker, Jonathan, Nizami, Zehra F., Yang, Xinxing, Ranjan, Rajesh, Urban, Elizabeth, Kim, Jee Min, Gall, Joseph, Xiao, Jie, Chen, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6684448/
https://www.ncbi.nlm.nih.gov/pubmed/31358945
http://dx.doi.org/10.1038/s41594-019-0269-z
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author Wooten, Matthew
Snedeker, Jonathan
Nizami, Zehra F.
Yang, Xinxing
Ranjan, Rajesh
Urban, Elizabeth
Kim, Jee Min
Gall, Joseph
Xiao, Jie
Chen, Xin
author_facet Wooten, Matthew
Snedeker, Jonathan
Nizami, Zehra F.
Yang, Xinxing
Ranjan, Rajesh
Urban, Elizabeth
Kim, Jee Min
Gall, Joseph
Xiao, Jie
Chen, Xin
author_sort Wooten, Matthew
collection PubMed
description Many stem cells undergo asymmetric division to produce a self-renewing stem cell and a differentiating daughter cell. Here we show that, similarly to H3, histone H4 is inherited asymmetrically in Drosophila melanogaster male germline stem cells undergoing asymmetric division. In contrast, both H2A and H2B are inherited symmetrically. By combining superresolution microscopy and chromatin fiber analyses with proximity ligation assays on intact nuclei, we find that old H3 is preferentially incorporated by the leading strand whereas newly synthesized H3 is enriched on the lagging strand. Using a sequential nucleoside analog incorporation assay, we detect a high incidence of unidirectional replication fork movement in testes-derived chromatin and DNA fibers. Biased fork movement coupled with a strand preference in histone incorporation would explain how asymmetric old and new H3 and H4 are established during replication. These results suggest a role for DNA replication in patterning epigenetic information in asymmetrically dividing cells in multicellular organisms.
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spelling pubmed-66844482020-01-29 Asymmetric histone inheritance via strand-specific incorporation and biased replication fork movement Wooten, Matthew Snedeker, Jonathan Nizami, Zehra F. Yang, Xinxing Ranjan, Rajesh Urban, Elizabeth Kim, Jee Min Gall, Joseph Xiao, Jie Chen, Xin Nat Struct Mol Biol Article Many stem cells undergo asymmetric division to produce a self-renewing stem cell and a differentiating daughter cell. Here we show that, similarly to H3, histone H4 is inherited asymmetrically in Drosophila melanogaster male germline stem cells undergoing asymmetric division. In contrast, both H2A and H2B are inherited symmetrically. By combining superresolution microscopy and chromatin fiber analyses with proximity ligation assays on intact nuclei, we find that old H3 is preferentially incorporated by the leading strand whereas newly synthesized H3 is enriched on the lagging strand. Using a sequential nucleoside analog incorporation assay, we detect a high incidence of unidirectional replication fork movement in testes-derived chromatin and DNA fibers. Biased fork movement coupled with a strand preference in histone incorporation would explain how asymmetric old and new H3 and H4 are established during replication. These results suggest a role for DNA replication in patterning epigenetic information in asymmetrically dividing cells in multicellular organisms. 2019-07-29 2019-08 /pmc/articles/PMC6684448/ /pubmed/31358945 http://dx.doi.org/10.1038/s41594-019-0269-z Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Wooten, Matthew
Snedeker, Jonathan
Nizami, Zehra F.
Yang, Xinxing
Ranjan, Rajesh
Urban, Elizabeth
Kim, Jee Min
Gall, Joseph
Xiao, Jie
Chen, Xin
Asymmetric histone inheritance via strand-specific incorporation and biased replication fork movement
title Asymmetric histone inheritance via strand-specific incorporation and biased replication fork movement
title_full Asymmetric histone inheritance via strand-specific incorporation and biased replication fork movement
title_fullStr Asymmetric histone inheritance via strand-specific incorporation and biased replication fork movement
title_full_unstemmed Asymmetric histone inheritance via strand-specific incorporation and biased replication fork movement
title_short Asymmetric histone inheritance via strand-specific incorporation and biased replication fork movement
title_sort asymmetric histone inheritance via strand-specific incorporation and biased replication fork movement
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6684448/
https://www.ncbi.nlm.nih.gov/pubmed/31358945
http://dx.doi.org/10.1038/s41594-019-0269-z
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