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Chromatin as self-returning walks: From population to single cell and back

With a growing understanding of the chromatin structure, many efforts remain focused on bridging the gap between what is suggested by population-averaged data and what is visualized for single cells. A popular approach to traversing these scales is to fit a polymer model to Hi-C contact data. Howeve...

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Autores principales: Shim, Anne R., Huang, Kai, Backman, Vadim, Szleifer, Igal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9680733/
https://www.ncbi.nlm.nih.gov/pubmed/36425085
http://dx.doi.org/10.1016/j.bpr.2021.100042
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author Shim, Anne R.
Huang, Kai
Backman, Vadim
Szleifer, Igal
author_facet Shim, Anne R.
Huang, Kai
Backman, Vadim
Szleifer, Igal
author_sort Shim, Anne R.
collection PubMed
description With a growing understanding of the chromatin structure, many efforts remain focused on bridging the gap between what is suggested by population-averaged data and what is visualized for single cells. A popular approach to traversing these scales is to fit a polymer model to Hi-C contact data. However, Hi-C is an average of millions to billions of cells, and each cell may not contain all population-averaged contacts. Therefore, we employ a novel approach of summing individual chromosome trajectories—determined by our Self-Returning Random Walk model—to create populations of cells. We allow single cells to consist of disparate structures and reproduce a variety of experimentally relevant contact maps. We show that the amount of shared topology between cells, and their mechanism of formation, changes the population-averaged structure. Therefore, we present a modeling technique that, with few constraints and little oversight, can be used to understand which single-cell chromatin structures underlie population-averaged behavior.
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spelling pubmed-96807332022-11-23 Chromatin as self-returning walks: From population to single cell and back Shim, Anne R. Huang, Kai Backman, Vadim Szleifer, Igal Biophys Rep (N Y) Letter With a growing understanding of the chromatin structure, many efforts remain focused on bridging the gap between what is suggested by population-averaged data and what is visualized for single cells. A popular approach to traversing these scales is to fit a polymer model to Hi-C contact data. However, Hi-C is an average of millions to billions of cells, and each cell may not contain all population-averaged contacts. Therefore, we employ a novel approach of summing individual chromosome trajectories—determined by our Self-Returning Random Walk model—to create populations of cells. We allow single cells to consist of disparate structures and reproduce a variety of experimentally relevant contact maps. We show that the amount of shared topology between cells, and their mechanism of formation, changes the population-averaged structure. Therefore, we present a modeling technique that, with few constraints and little oversight, can be used to understand which single-cell chromatin structures underlie population-averaged behavior. Elsevier 2021-12-10 /pmc/articles/PMC9680733/ /pubmed/36425085 http://dx.doi.org/10.1016/j.bpr.2021.100042 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Letter
Shim, Anne R.
Huang, Kai
Backman, Vadim
Szleifer, Igal
Chromatin as self-returning walks: From population to single cell and back
title Chromatin as self-returning walks: From population to single cell and back
title_full Chromatin as self-returning walks: From population to single cell and back
title_fullStr Chromatin as self-returning walks: From population to single cell and back
title_full_unstemmed Chromatin as self-returning walks: From population to single cell and back
title_short Chromatin as self-returning walks: From population to single cell and back
title_sort chromatin as self-returning walks: from population to single cell and back
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9680733/
https://www.ncbi.nlm.nih.gov/pubmed/36425085
http://dx.doi.org/10.1016/j.bpr.2021.100042
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