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Behavior of dicentric chromosomes in budding yeast
DNA double-strand breaks arise in vivo when a dicentric chromosome (two centromeres on one chromosome) goes through mitosis with the two centromeres attached to opposite spindle pole bodies. Repair of the DSBs generates phenotypic diversity due to the range of monocentric derivative chromosomes that...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8009378/ https://www.ncbi.nlm.nih.gov/pubmed/33735169 http://dx.doi.org/10.1371/journal.pgen.1009442 |
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author | Cook, Diana Long, Sarah Stanton, John Cusick, Patrick Lawrimore, Colleen Yeh, Elaine Grant, Sarah Bloom, Kerry |
author_facet | Cook, Diana Long, Sarah Stanton, John Cusick, Patrick Lawrimore, Colleen Yeh, Elaine Grant, Sarah Bloom, Kerry |
author_sort | Cook, Diana |
collection | PubMed |
description | DNA double-strand breaks arise in vivo when a dicentric chromosome (two centromeres on one chromosome) goes through mitosis with the two centromeres attached to opposite spindle pole bodies. Repair of the DSBs generates phenotypic diversity due to the range of monocentric derivative chromosomes that arise. To explore whether DSBs may be differentially repaired as a function of their spatial position in the chromosome, we have examined the structure of monocentric derivative chromosomes from cells containing a suite of dicentric chromosomes in which the distance between the two centromeres ranges from 6.5 kb to 57.7 kb. Two major classes of repair products, homology-based (homologous recombination (HR) and single-strand annealing (SSA)) and end-joining (non-homologous (NHEJ) and micro-homology mediated (MMEJ)) were identified. The distribution of repair products varies as a function of distance between the two centromeres. Genetic dependencies on double strand break repair (Rad52), DNA ligase (Lif1), and S phase checkpoint (Mrc1) are indicative of distinct repair pathway choices for DNA breaks in the pericentromeric chromatin versus the arms. |
format | Online Article Text |
id | pubmed-8009378 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-80093782021-04-07 Behavior of dicentric chromosomes in budding yeast Cook, Diana Long, Sarah Stanton, John Cusick, Patrick Lawrimore, Colleen Yeh, Elaine Grant, Sarah Bloom, Kerry PLoS Genet Research Article DNA double-strand breaks arise in vivo when a dicentric chromosome (two centromeres on one chromosome) goes through mitosis with the two centromeres attached to opposite spindle pole bodies. Repair of the DSBs generates phenotypic diversity due to the range of monocentric derivative chromosomes that arise. To explore whether DSBs may be differentially repaired as a function of their spatial position in the chromosome, we have examined the structure of monocentric derivative chromosomes from cells containing a suite of dicentric chromosomes in which the distance between the two centromeres ranges from 6.5 kb to 57.7 kb. Two major classes of repair products, homology-based (homologous recombination (HR) and single-strand annealing (SSA)) and end-joining (non-homologous (NHEJ) and micro-homology mediated (MMEJ)) were identified. The distribution of repair products varies as a function of distance between the two centromeres. Genetic dependencies on double strand break repair (Rad52), DNA ligase (Lif1), and S phase checkpoint (Mrc1) are indicative of distinct repair pathway choices for DNA breaks in the pericentromeric chromatin versus the arms. Public Library of Science 2021-03-18 /pmc/articles/PMC8009378/ /pubmed/33735169 http://dx.doi.org/10.1371/journal.pgen.1009442 Text en © 2021 Cook et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Cook, Diana Long, Sarah Stanton, John Cusick, Patrick Lawrimore, Colleen Yeh, Elaine Grant, Sarah Bloom, Kerry Behavior of dicentric chromosomes in budding yeast |
title | Behavior of dicentric chromosomes in budding yeast |
title_full | Behavior of dicentric chromosomes in budding yeast |
title_fullStr | Behavior of dicentric chromosomes in budding yeast |
title_full_unstemmed | Behavior of dicentric chromosomes in budding yeast |
title_short | Behavior of dicentric chromosomes in budding yeast |
title_sort | behavior of dicentric chromosomes in budding yeast |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8009378/ https://www.ncbi.nlm.nih.gov/pubmed/33735169 http://dx.doi.org/10.1371/journal.pgen.1009442 |
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