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Asymmetric chromatin retention and nuclear envelopes separate chromosomes in fused cells in vivo
Hybrid cells derived through fertilization or somatic cell fusion recognize and separate chromosomes of different origins. The underlying mechanisms are unknown but could prevent aneuploidy and tumor formation. Here, we acutely induce fusion between Drosophila neural stem cells (neuroblasts; NBs) an...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9485224/ https://www.ncbi.nlm.nih.gov/pubmed/36123528 http://dx.doi.org/10.1038/s42003-022-03874-z |
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author | Sunchu, Bharath Lee, Nicole MynYi Taylor, Jennifer A. Segura, Roberto Carlos Roubinet, Chantal Cabernard, Clemens |
author_facet | Sunchu, Bharath Lee, Nicole MynYi Taylor, Jennifer A. Segura, Roberto Carlos Roubinet, Chantal Cabernard, Clemens |
author_sort | Sunchu, Bharath |
collection | PubMed |
description | Hybrid cells derived through fertilization or somatic cell fusion recognize and separate chromosomes of different origins. The underlying mechanisms are unknown but could prevent aneuploidy and tumor formation. Here, we acutely induce fusion between Drosophila neural stem cells (neuroblasts; NBs) and differentiating ganglion mother cells (GMCs) in vivo to define how epigenetically distinct chromatin is recognized and segregated. We find that NB-GMC hybrid cells align both endogenous (neuroblast-origin) and ectopic (GMC-origin) chromosomes at the metaphase plate through centrosome derived dual-spindles. Physical separation of endogenous and ectopic chromatin is achieved through asymmetric, microtubule-dependent chromatin retention in interphase and physical boundaries imposed by nuclear envelopes. The chromatin separation mechanisms described here could apply to the first zygotic division in insects, arthropods, and vertebrates or potentially inform biased chromatid segregation in stem cells. |
format | Online Article Text |
id | pubmed-9485224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-94852242022-09-21 Asymmetric chromatin retention and nuclear envelopes separate chromosomes in fused cells in vivo Sunchu, Bharath Lee, Nicole MynYi Taylor, Jennifer A. Segura, Roberto Carlos Roubinet, Chantal Cabernard, Clemens Commun Biol Article Hybrid cells derived through fertilization or somatic cell fusion recognize and separate chromosomes of different origins. The underlying mechanisms are unknown but could prevent aneuploidy and tumor formation. Here, we acutely induce fusion between Drosophila neural stem cells (neuroblasts; NBs) and differentiating ganglion mother cells (GMCs) in vivo to define how epigenetically distinct chromatin is recognized and segregated. We find that NB-GMC hybrid cells align both endogenous (neuroblast-origin) and ectopic (GMC-origin) chromosomes at the metaphase plate through centrosome derived dual-spindles. Physical separation of endogenous and ectopic chromatin is achieved through asymmetric, microtubule-dependent chromatin retention in interphase and physical boundaries imposed by nuclear envelopes. The chromatin separation mechanisms described here could apply to the first zygotic division in insects, arthropods, and vertebrates or potentially inform biased chromatid segregation in stem cells. Nature Publishing Group UK 2022-09-19 /pmc/articles/PMC9485224/ /pubmed/36123528 http://dx.doi.org/10.1038/s42003-022-03874-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Sunchu, Bharath Lee, Nicole MynYi Taylor, Jennifer A. Segura, Roberto Carlos Roubinet, Chantal Cabernard, Clemens Asymmetric chromatin retention and nuclear envelopes separate chromosomes in fused cells in vivo |
title | Asymmetric chromatin retention and nuclear envelopes separate chromosomes in fused cells in vivo |
title_full | Asymmetric chromatin retention and nuclear envelopes separate chromosomes in fused cells in vivo |
title_fullStr | Asymmetric chromatin retention and nuclear envelopes separate chromosomes in fused cells in vivo |
title_full_unstemmed | Asymmetric chromatin retention and nuclear envelopes separate chromosomes in fused cells in vivo |
title_short | Asymmetric chromatin retention and nuclear envelopes separate chromosomes in fused cells in vivo |
title_sort | asymmetric chromatin retention and nuclear envelopes separate chromosomes in fused cells in vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9485224/ https://www.ncbi.nlm.nih.gov/pubmed/36123528 http://dx.doi.org/10.1038/s42003-022-03874-z |
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