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Spatially mapped single-cell chromatin accessibility
High-throughput single-cell epigenomic assays can resolve cell type heterogeneity in complex tissues, however, spatial orientation is lost. Here, we present single-cell combinatorial indexing on Microbiopsies Assigned to Positions for the Assay for Transposase Accessible Chromatin, or sciMAP-ATAC, a...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904839/ https://www.ncbi.nlm.nih.gov/pubmed/33627658 http://dx.doi.org/10.1038/s41467-021-21515-7 |
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author | Thornton, Casey A. Mulqueen, Ryan M. Torkenczy, Kristof A. Nishida, Andrew Lowenstein, Eve G. Fields, Andrew J. Steemers, Frank J. Zhang, Wenri McConnell, Heather L. Woltjer, Randy L. Mishra, Anusha Wright, Kevin M. Adey, Andrew C. |
author_facet | Thornton, Casey A. Mulqueen, Ryan M. Torkenczy, Kristof A. Nishida, Andrew Lowenstein, Eve G. Fields, Andrew J. Steemers, Frank J. Zhang, Wenri McConnell, Heather L. Woltjer, Randy L. Mishra, Anusha Wright, Kevin M. Adey, Andrew C. |
author_sort | Thornton, Casey A. |
collection | PubMed |
description | High-throughput single-cell epigenomic assays can resolve cell type heterogeneity in complex tissues, however, spatial orientation is lost. Here, we present single-cell combinatorial indexing on Microbiopsies Assigned to Positions for the Assay for Transposase Accessible Chromatin, or sciMAP-ATAC, as a method for highly scalable, spatially resolved, single-cell profiling of chromatin states. sciMAP-ATAC produces data of equivalent quality to non-spatial sci-ATAC and retains the positional information of each cell within a 214 micron cubic region, with up to hundreds of tracked positions in a single experiment. We apply sciMAP-ATAC to assess cortical lamination in the adult mouse primary somatosensory cortex and in the human primary visual cortex, where we produce spatial trajectories and integrate our data with non-spatial single-nucleus RNA and other chromatin accessibility single-cell datasets. Finally, we characterize the spatially progressive nature of cerebral ischemic infarction in the mouse brain using a model of transient middle cerebral artery occlusion. |
format | Online Article Text |
id | pubmed-7904839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79048392021-03-11 Spatially mapped single-cell chromatin accessibility Thornton, Casey A. Mulqueen, Ryan M. Torkenczy, Kristof A. Nishida, Andrew Lowenstein, Eve G. Fields, Andrew J. Steemers, Frank J. Zhang, Wenri McConnell, Heather L. Woltjer, Randy L. Mishra, Anusha Wright, Kevin M. Adey, Andrew C. Nat Commun Article High-throughput single-cell epigenomic assays can resolve cell type heterogeneity in complex tissues, however, spatial orientation is lost. Here, we present single-cell combinatorial indexing on Microbiopsies Assigned to Positions for the Assay for Transposase Accessible Chromatin, or sciMAP-ATAC, as a method for highly scalable, spatially resolved, single-cell profiling of chromatin states. sciMAP-ATAC produces data of equivalent quality to non-spatial sci-ATAC and retains the positional information of each cell within a 214 micron cubic region, with up to hundreds of tracked positions in a single experiment. We apply sciMAP-ATAC to assess cortical lamination in the adult mouse primary somatosensory cortex and in the human primary visual cortex, where we produce spatial trajectories and integrate our data with non-spatial single-nucleus RNA and other chromatin accessibility single-cell datasets. Finally, we characterize the spatially progressive nature of cerebral ischemic infarction in the mouse brain using a model of transient middle cerebral artery occlusion. Nature Publishing Group UK 2021-02-24 /pmc/articles/PMC7904839/ /pubmed/33627658 http://dx.doi.org/10.1038/s41467-021-21515-7 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 Thornton, Casey A. Mulqueen, Ryan M. Torkenczy, Kristof A. Nishida, Andrew Lowenstein, Eve G. Fields, Andrew J. Steemers, Frank J. Zhang, Wenri McConnell, Heather L. Woltjer, Randy L. Mishra, Anusha Wright, Kevin M. Adey, Andrew C. Spatially mapped single-cell chromatin accessibility |
title | Spatially mapped single-cell chromatin accessibility |
title_full | Spatially mapped single-cell chromatin accessibility |
title_fullStr | Spatially mapped single-cell chromatin accessibility |
title_full_unstemmed | Spatially mapped single-cell chromatin accessibility |
title_short | Spatially mapped single-cell chromatin accessibility |
title_sort | spatially mapped single-cell chromatin accessibility |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904839/ https://www.ncbi.nlm.nih.gov/pubmed/33627658 http://dx.doi.org/10.1038/s41467-021-21515-7 |
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