Cargando…

A simple model explains the cell cycle-dependent assembly of centromeric nucleosomes in holocentric species

Centromeres are essential for chromosome movement. In independent taxa, species with holocentric chromosomes exist. In contrast to monocentric species, where no obvious dispersion of centromeres occurs during interphase, the organization of holocentromeres differs between condensed and decondensed c...

Descripción completa

Detalles Bibliográficos
Autores principales: Câmara, Amanda Souza, Schubert, Veit, Mascher, Martin, Houben, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450114/
https://www.ncbi.nlm.nih.gov/pubmed/34352103
http://dx.doi.org/10.1093/nar/gkab648
_version_ 1784569559125065728
author Câmara, Amanda Souza
Schubert, Veit
Mascher, Martin
Houben, Andreas
author_facet Câmara, Amanda Souza
Schubert, Veit
Mascher, Martin
Houben, Andreas
author_sort Câmara, Amanda Souza
collection PubMed
description Centromeres are essential for chromosome movement. In independent taxa, species with holocentric chromosomes exist. In contrast to monocentric species, where no obvious dispersion of centromeres occurs during interphase, the organization of holocentromeres differs between condensed and decondensed chromosomes. During interphase, centromeres are dispersed into a large number of CENH3-positive nucleosome clusters in a number of holocentric species. With the onset of chromosome condensation, the centromeric nucleosomes join and form line-like holocentromeres. Using polymer simulations, we propose a mechanism relying on the interaction between centromeric nucleosomes and structural maintenance of chromosomes (SMC) proteins. Different sets of molecular dynamic simulations were evaluated by testing four parameters: (i) the concentration of Loop Extruders (LEs) corresponding to SMCs, (ii) the distribution and number of centromeric nucleosomes, (iii) the effect of centromeric nucleosomes on interacting LEs and (iv) the assembly of kinetochores bound to centromeric nucleosomes. We observed the formation of a line-like holocentromere, due to the aggregation of the centromeric nucleosomes when the chromosome was compacted into loops. A groove-like holocentromere structure formed after a kinetochore complex was simulated along the centromeric line. Similar mechanisms may also organize a monocentric chromosome constriction, and its regulation may cause different centromere types during evolution.
format Online
Article
Text
id pubmed-8450114
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-84501142021-09-20 A simple model explains the cell cycle-dependent assembly of centromeric nucleosomes in holocentric species Câmara, Amanda Souza Schubert, Veit Mascher, Martin Houben, Andreas Nucleic Acids Res Computational Biology Centromeres are essential for chromosome movement. In independent taxa, species with holocentric chromosomes exist. In contrast to monocentric species, where no obvious dispersion of centromeres occurs during interphase, the organization of holocentromeres differs between condensed and decondensed chromosomes. During interphase, centromeres are dispersed into a large number of CENH3-positive nucleosome clusters in a number of holocentric species. With the onset of chromosome condensation, the centromeric nucleosomes join and form line-like holocentromeres. Using polymer simulations, we propose a mechanism relying on the interaction between centromeric nucleosomes and structural maintenance of chromosomes (SMC) proteins. Different sets of molecular dynamic simulations were evaluated by testing four parameters: (i) the concentration of Loop Extruders (LEs) corresponding to SMCs, (ii) the distribution and number of centromeric nucleosomes, (iii) the effect of centromeric nucleosomes on interacting LEs and (iv) the assembly of kinetochores bound to centromeric nucleosomes. We observed the formation of a line-like holocentromere, due to the aggregation of the centromeric nucleosomes when the chromosome was compacted into loops. A groove-like holocentromere structure formed after a kinetochore complex was simulated along the centromeric line. Similar mechanisms may also organize a monocentric chromosome constriction, and its regulation may cause different centromere types during evolution. Oxford University Press 2021-08-05 /pmc/articles/PMC8450114/ /pubmed/34352103 http://dx.doi.org/10.1093/nar/gkab648 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Computational Biology
Câmara, Amanda Souza
Schubert, Veit
Mascher, Martin
Houben, Andreas
A simple model explains the cell cycle-dependent assembly of centromeric nucleosomes in holocentric species
title A simple model explains the cell cycle-dependent assembly of centromeric nucleosomes in holocentric species
title_full A simple model explains the cell cycle-dependent assembly of centromeric nucleosomes in holocentric species
title_fullStr A simple model explains the cell cycle-dependent assembly of centromeric nucleosomes in holocentric species
title_full_unstemmed A simple model explains the cell cycle-dependent assembly of centromeric nucleosomes in holocentric species
title_short A simple model explains the cell cycle-dependent assembly of centromeric nucleosomes in holocentric species
title_sort simple model explains the cell cycle-dependent assembly of centromeric nucleosomes in holocentric species
topic Computational Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450114/
https://www.ncbi.nlm.nih.gov/pubmed/34352103
http://dx.doi.org/10.1093/nar/gkab648
work_keys_str_mv AT camaraamandasouza asimplemodelexplainsthecellcycledependentassemblyofcentromericnucleosomesinholocentricspecies
AT schubertveit asimplemodelexplainsthecellcycledependentassemblyofcentromericnucleosomesinholocentricspecies
AT maschermartin asimplemodelexplainsthecellcycledependentassemblyofcentromericnucleosomesinholocentricspecies
AT houbenandreas asimplemodelexplainsthecellcycledependentassemblyofcentromericnucleosomesinholocentricspecies
AT camaraamandasouza simplemodelexplainsthecellcycledependentassemblyofcentromericnucleosomesinholocentricspecies
AT schubertveit simplemodelexplainsthecellcycledependentassemblyofcentromericnucleosomesinholocentricspecies
AT maschermartin simplemodelexplainsthecellcycledependentassemblyofcentromericnucleosomesinholocentricspecies
AT houbenandreas simplemodelexplainsthecellcycledependentassemblyofcentromericnucleosomesinholocentricspecies