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The Chd1 chromatin remodeler can sense both entry and exit sides of the nucleosome

Chromatin remodelers are essential for establishing and maintaining the placement of nucleosomes along genomic DNA. Yet how chromatin remodelers recognize and respond to distinct chromatin environments surrounding nucleosomes is poorly understood. Here, we use Lac repressor as a tool to probe how a...

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Autores principales: Nodelman, Ilana M., Horvath, Kyle C., Levendosky, Robert F., Winger, Jessica, Ren, Ren, Patel, Ashok, Li, Ming, Wang, Michelle D., Roberts, Elijah, Bowman, Gregory D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5027475/
https://www.ncbi.nlm.nih.gov/pubmed/27174939
http://dx.doi.org/10.1093/nar/gkw406
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author Nodelman, Ilana M.
Horvath, Kyle C.
Levendosky, Robert F.
Winger, Jessica
Ren, Ren
Patel, Ashok
Li, Ming
Wang, Michelle D.
Roberts, Elijah
Bowman, Gregory D.
author_facet Nodelman, Ilana M.
Horvath, Kyle C.
Levendosky, Robert F.
Winger, Jessica
Ren, Ren
Patel, Ashok
Li, Ming
Wang, Michelle D.
Roberts, Elijah
Bowman, Gregory D.
author_sort Nodelman, Ilana M.
collection PubMed
description Chromatin remodelers are essential for establishing and maintaining the placement of nucleosomes along genomic DNA. Yet how chromatin remodelers recognize and respond to distinct chromatin environments surrounding nucleosomes is poorly understood. Here, we use Lac repressor as a tool to probe how a DNA-bound factor influences action of the Chd1 remodeler. We show that Chd1 preferentially shifts nucleosomes away from Lac repressor, demonstrating that a DNA-bound factor defines a barrier for nucleosome positioning. Rather than an absolute block in sliding, the barrier effect was achieved by altered rates of nucleosome sliding that biased redistribution of nucleosomes away from the bound Lac repressor site. Remarkably, in addition to slower sliding toward the LacO site, the presence of Lac repressor also stimulated sliding in the opposite direction. These experiments therefore demonstrate that Chd1 responds to the presence of a bound protein on both entry and exit sides of the nucleosome. This sensitivity to both sides of the nucleosome allows for a faster and sharper response than would be possible by responding to only the entry side, and we speculate that dual entry/exit sensitivity is also important for regularly spaced nucleosome arrays generated by Chd1 and the related ISWI remodelers.
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spelling pubmed-50274752016-09-21 The Chd1 chromatin remodeler can sense both entry and exit sides of the nucleosome Nodelman, Ilana M. Horvath, Kyle C. Levendosky, Robert F. Winger, Jessica Ren, Ren Patel, Ashok Li, Ming Wang, Michelle D. Roberts, Elijah Bowman, Gregory D. Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Chromatin remodelers are essential for establishing and maintaining the placement of nucleosomes along genomic DNA. Yet how chromatin remodelers recognize and respond to distinct chromatin environments surrounding nucleosomes is poorly understood. Here, we use Lac repressor as a tool to probe how a DNA-bound factor influences action of the Chd1 remodeler. We show that Chd1 preferentially shifts nucleosomes away from Lac repressor, demonstrating that a DNA-bound factor defines a barrier for nucleosome positioning. Rather than an absolute block in sliding, the barrier effect was achieved by altered rates of nucleosome sliding that biased redistribution of nucleosomes away from the bound Lac repressor site. Remarkably, in addition to slower sliding toward the LacO site, the presence of Lac repressor also stimulated sliding in the opposite direction. These experiments therefore demonstrate that Chd1 responds to the presence of a bound protein on both entry and exit sides of the nucleosome. This sensitivity to both sides of the nucleosome allows for a faster and sharper response than would be possible by responding to only the entry side, and we speculate that dual entry/exit sensitivity is also important for regularly spaced nucleosome arrays generated by Chd1 and the related ISWI remodelers. Oxford University Press 2016-09-19 2016-05-12 /pmc/articles/PMC5027475/ /pubmed/27174939 http://dx.doi.org/10.1093/nar/gkw406 Text en © The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Gene regulation, Chromatin and Epigenetics
Nodelman, Ilana M.
Horvath, Kyle C.
Levendosky, Robert F.
Winger, Jessica
Ren, Ren
Patel, Ashok
Li, Ming
Wang, Michelle D.
Roberts, Elijah
Bowman, Gregory D.
The Chd1 chromatin remodeler can sense both entry and exit sides of the nucleosome
title The Chd1 chromatin remodeler can sense both entry and exit sides of the nucleosome
title_full The Chd1 chromatin remodeler can sense both entry and exit sides of the nucleosome
title_fullStr The Chd1 chromatin remodeler can sense both entry and exit sides of the nucleosome
title_full_unstemmed The Chd1 chromatin remodeler can sense both entry and exit sides of the nucleosome
title_short The Chd1 chromatin remodeler can sense both entry and exit sides of the nucleosome
title_sort chd1 chromatin remodeler can sense both entry and exit sides of the nucleosome
topic Gene regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5027475/
https://www.ncbi.nlm.nih.gov/pubmed/27174939
http://dx.doi.org/10.1093/nar/gkw406
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