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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...

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Autores principales: Sunchu, Bharath, Lee, Nicole MynYi, Taylor, Jennifer A., Segura, Roberto Carlos, Roubinet, Chantal, Cabernard, Clemens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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.
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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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