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High-resolution mapping of centromeric protein association using APEX-chromatin fibers
BACKGROUND: The centromere is a specialized chromosomal locus that forms the basis for the assembly of a multi-protein complex, the kinetochore and ensures faithful chromosome segregation during every cell division. The repetitive nature of the underlying centromeric sequence represents a major obst...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6238281/ https://www.ncbi.nlm.nih.gov/pubmed/30445992 http://dx.doi.org/10.1186/s13072-018-0237-6 |
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author | Kyriacou, Eftychia Heun, Patrick |
author_facet | Kyriacou, Eftychia Heun, Patrick |
author_sort | Kyriacou, Eftychia |
collection | PubMed |
description | BACKGROUND: The centromere is a specialized chromosomal locus that forms the basis for the assembly of a multi-protein complex, the kinetochore and ensures faithful chromosome segregation during every cell division. The repetitive nature of the underlying centromeric sequence represents a major obstacle for high-resolution mapping of protein binding using methods that rely on annotated genomes. Here, we present a novel microscopy-based approach called “APEX-chromatin fibers” for localizing protein binding over the repetitive centromeric sequences at kilobase resolution. RESULTS: By fusing centromere factors of interest to ascorbate peroxidase, we were able to label their binding profiles on extended chromatin fibers with biotin marks. We applied APEX-chromatin fibers to at least one member of each CCAN complex, most of which show a localization pattern different from CENP-A but within the CENP-A delineated centromeric domain. Interestingly, we describe here a novel characteristic of CENP-I and CENP-B that display extended localization beyond the CENP-A boundaries. CONCLUSIONS: Our approach was successfully applied for mapping protein association over centromeric chromatin, revealing previously undescribed localization patterns. In this study, we focused on centromeric factors, but we believe that this approach could be useful for mapping protein binding patterns in other repetitive regions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13072-018-0237-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6238281 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62382812018-11-23 High-resolution mapping of centromeric protein association using APEX-chromatin fibers Kyriacou, Eftychia Heun, Patrick Epigenetics Chromatin Methodology BACKGROUND: The centromere is a specialized chromosomal locus that forms the basis for the assembly of a multi-protein complex, the kinetochore and ensures faithful chromosome segregation during every cell division. The repetitive nature of the underlying centromeric sequence represents a major obstacle for high-resolution mapping of protein binding using methods that rely on annotated genomes. Here, we present a novel microscopy-based approach called “APEX-chromatin fibers” for localizing protein binding over the repetitive centromeric sequences at kilobase resolution. RESULTS: By fusing centromere factors of interest to ascorbate peroxidase, we were able to label their binding profiles on extended chromatin fibers with biotin marks. We applied APEX-chromatin fibers to at least one member of each CCAN complex, most of which show a localization pattern different from CENP-A but within the CENP-A delineated centromeric domain. Interestingly, we describe here a novel characteristic of CENP-I and CENP-B that display extended localization beyond the CENP-A boundaries. CONCLUSIONS: Our approach was successfully applied for mapping protein association over centromeric chromatin, revealing previously undescribed localization patterns. In this study, we focused on centromeric factors, but we believe that this approach could be useful for mapping protein binding patterns in other repetitive regions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13072-018-0237-6) contains supplementary material, which is available to authorized users. BioMed Central 2018-11-16 /pmc/articles/PMC6238281/ /pubmed/30445992 http://dx.doi.org/10.1186/s13072-018-0237-6 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Kyriacou, Eftychia Heun, Patrick High-resolution mapping of centromeric protein association using APEX-chromatin fibers |
title | High-resolution mapping of centromeric protein association using APEX-chromatin fibers |
title_full | High-resolution mapping of centromeric protein association using APEX-chromatin fibers |
title_fullStr | High-resolution mapping of centromeric protein association using APEX-chromatin fibers |
title_full_unstemmed | High-resolution mapping of centromeric protein association using APEX-chromatin fibers |
title_short | High-resolution mapping of centromeric protein association using APEX-chromatin fibers |
title_sort | high-resolution mapping of centromeric protein association using apex-chromatin fibers |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6238281/ https://www.ncbi.nlm.nih.gov/pubmed/30445992 http://dx.doi.org/10.1186/s13072-018-0237-6 |
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