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Learning the distribution of single-cell chromosome conformations in bacteria reveals emergent order across genomic scales

The order and variability of bacterial chromosome organization, contained within the distribution of chromosome conformations, are unclear. Here, we develop a fully data-driven maximum entropy approach to extract single-cell 3D chromosome conformations from Hi–C experiments on the model organism Cau...

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Autores principales: Messelink, Joris J. B., van Teeseling, Muriel C. F., Janssen, Jacqueline, Thanbichler, Martin, Broedersz, Chase P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8010069/
https://www.ncbi.nlm.nih.gov/pubmed/33785756
http://dx.doi.org/10.1038/s41467-021-22189-x
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author Messelink, Joris J. B.
van Teeseling, Muriel C. F.
Janssen, Jacqueline
Thanbichler, Martin
Broedersz, Chase P.
author_facet Messelink, Joris J. B.
van Teeseling, Muriel C. F.
Janssen, Jacqueline
Thanbichler, Martin
Broedersz, Chase P.
author_sort Messelink, Joris J. B.
collection PubMed
description The order and variability of bacterial chromosome organization, contained within the distribution of chromosome conformations, are unclear. Here, we develop a fully data-driven maximum entropy approach to extract single-cell 3D chromosome conformations from Hi–C experiments on the model organism Caulobacter crescentus. The predictive power of our model is validated by independent experiments. We find that on large genomic scales, organizational features are predominantly present along the long cell axis: chromosomal loci exhibit striking long-ranged two-point axial correlations, indicating emergent order. This organization is associated with large genomic clusters we term Super Domains (SuDs), whose existence we support with super-resolution microscopy. On smaller genomic scales, our model reveals chromosome extensions that correlate with transcriptional and loop extrusion activity. Finally, we quantify the information contained in chromosome organization that may guide cellular processes. Our approach can be extended to other species, providing a general strategy to resolve variability in single-cell chromosomal organization.
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spelling pubmed-80100692021-04-16 Learning the distribution of single-cell chromosome conformations in bacteria reveals emergent order across genomic scales Messelink, Joris J. B. van Teeseling, Muriel C. F. Janssen, Jacqueline Thanbichler, Martin Broedersz, Chase P. Nat Commun Article The order and variability of bacterial chromosome organization, contained within the distribution of chromosome conformations, are unclear. Here, we develop a fully data-driven maximum entropy approach to extract single-cell 3D chromosome conformations from Hi–C experiments on the model organism Caulobacter crescentus. The predictive power of our model is validated by independent experiments. We find that on large genomic scales, organizational features are predominantly present along the long cell axis: chromosomal loci exhibit striking long-ranged two-point axial correlations, indicating emergent order. This organization is associated with large genomic clusters we term Super Domains (SuDs), whose existence we support with super-resolution microscopy. On smaller genomic scales, our model reveals chromosome extensions that correlate with transcriptional and loop extrusion activity. Finally, we quantify the information contained in chromosome organization that may guide cellular processes. Our approach can be extended to other species, providing a general strategy to resolve variability in single-cell chromosomal organization. Nature Publishing Group UK 2021-03-30 /pmc/articles/PMC8010069/ /pubmed/33785756 http://dx.doi.org/10.1038/s41467-021-22189-x Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Messelink, Joris J. B.
van Teeseling, Muriel C. F.
Janssen, Jacqueline
Thanbichler, Martin
Broedersz, Chase P.
Learning the distribution of single-cell chromosome conformations in bacteria reveals emergent order across genomic scales
title Learning the distribution of single-cell chromosome conformations in bacteria reveals emergent order across genomic scales
title_full Learning the distribution of single-cell chromosome conformations in bacteria reveals emergent order across genomic scales
title_fullStr Learning the distribution of single-cell chromosome conformations in bacteria reveals emergent order across genomic scales
title_full_unstemmed Learning the distribution of single-cell chromosome conformations in bacteria reveals emergent order across genomic scales
title_short Learning the distribution of single-cell chromosome conformations in bacteria reveals emergent order across genomic scales
title_sort learning the distribution of single-cell chromosome conformations in bacteria reveals emergent order across genomic scales
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8010069/
https://www.ncbi.nlm.nih.gov/pubmed/33785756
http://dx.doi.org/10.1038/s41467-021-22189-x
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