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R-loops at centromeric chromatin contribute to defects in kinetochore integrity and chromosomal instability in budding yeast
R-loops, the byproduct of DNA–RNA hybridization and the displaced single-stranded DNA (ssDNA), have been identified in bacteria, yeasts, and other eukaryotic organisms. The persistent presence of R-loops contributes to defects in DNA replication and repair, gene expression, and genomic integrity. R-...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The American Society for Cell Biology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8098821/ https://www.ncbi.nlm.nih.gov/pubmed/33147102 http://dx.doi.org/10.1091/mbc.E20-06-0379 |
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author | Mishra, Prashant K. Chakraborty, Arijita Yeh, Elaine Feng, Wenyi Bloom, Kerry S. Basrai, Munira A. |
author_facet | Mishra, Prashant K. Chakraborty, Arijita Yeh, Elaine Feng, Wenyi Bloom, Kerry S. Basrai, Munira A. |
author_sort | Mishra, Prashant K. |
collection | PubMed |
description | R-loops, the byproduct of DNA–RNA hybridization and the displaced single-stranded DNA (ssDNA), have been identified in bacteria, yeasts, and other eukaryotic organisms. The persistent presence of R-loops contributes to defects in DNA replication and repair, gene expression, and genomic integrity. R-loops have not been detected at centromeric (CEN) chromatin in wild-type budding yeast. Here we used an hpr1∆ strain that accumulates R-loops to investigate the consequences of R-loops at CEN chromatin and chromosome segregation. We show that Hpr1 interacts with the CEN-histone H3 variant, Cse4, and prevents the accumulation of R-loops at CEN chromatin for chromosomal stability. DNA–RNA immunoprecipitation (DRIP) analysis showed an accumulation of R-loops at CEN chromatin that was reduced by overexpression of RNH1 in hpr1∆ strains. Increased levels of ssDNA, reduced levels of Cse4 and its assembly factor Scm3, and mislocalization of histone H3 at CEN chromatin were observed in hpr1∆ strains. We determined that accumulation of R-loops at CEN chromatin contributes to defects in kinetochore biorientation and chromosomal instability (CIN) and these phenotypes are suppressed by RNH1 overexpression in hpr1∆ strains. In summary, our studies provide mechanistic insights into how accumulation of R-loops at CEN contributes to defects in kinetochore integrity and CIN. |
format | Online Article Text |
id | pubmed-8098821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-80988212021-05-05 R-loops at centromeric chromatin contribute to defects in kinetochore integrity and chromosomal instability in budding yeast Mishra, Prashant K. Chakraborty, Arijita Yeh, Elaine Feng, Wenyi Bloom, Kerry S. Basrai, Munira A. Mol Biol Cell Articles R-loops, the byproduct of DNA–RNA hybridization and the displaced single-stranded DNA (ssDNA), have been identified in bacteria, yeasts, and other eukaryotic organisms. The persistent presence of R-loops contributes to defects in DNA replication and repair, gene expression, and genomic integrity. R-loops have not been detected at centromeric (CEN) chromatin in wild-type budding yeast. Here we used an hpr1∆ strain that accumulates R-loops to investigate the consequences of R-loops at CEN chromatin and chromosome segregation. We show that Hpr1 interacts with the CEN-histone H3 variant, Cse4, and prevents the accumulation of R-loops at CEN chromatin for chromosomal stability. DNA–RNA immunoprecipitation (DRIP) analysis showed an accumulation of R-loops at CEN chromatin that was reduced by overexpression of RNH1 in hpr1∆ strains. Increased levels of ssDNA, reduced levels of Cse4 and its assembly factor Scm3, and mislocalization of histone H3 at CEN chromatin were observed in hpr1∆ strains. We determined that accumulation of R-loops at CEN chromatin contributes to defects in kinetochore biorientation and chromosomal instability (CIN) and these phenotypes are suppressed by RNH1 overexpression in hpr1∆ strains. In summary, our studies provide mechanistic insights into how accumulation of R-loops at CEN contributes to defects in kinetochore integrity and CIN. The American Society for Cell Biology 2021-01-01 /pmc/articles/PMC8098821/ /pubmed/33147102 http://dx.doi.org/10.1091/mbc.E20-06-0379 Text en © 2021 Mishra et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/3.0/This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License. |
spellingShingle | Articles Mishra, Prashant K. Chakraborty, Arijita Yeh, Elaine Feng, Wenyi Bloom, Kerry S. Basrai, Munira A. R-loops at centromeric chromatin contribute to defects in kinetochore integrity and chromosomal instability in budding yeast |
title | R-loops at centromeric chromatin contribute to defects in kinetochore integrity and chromosomal instability in budding yeast |
title_full | R-loops at centromeric chromatin contribute to defects in kinetochore integrity and chromosomal instability in budding yeast |
title_fullStr | R-loops at centromeric chromatin contribute to defects in kinetochore integrity and chromosomal instability in budding yeast |
title_full_unstemmed | R-loops at centromeric chromatin contribute to defects in kinetochore integrity and chromosomal instability in budding yeast |
title_short | R-loops at centromeric chromatin contribute to defects in kinetochore integrity and chromosomal instability in budding yeast |
title_sort | r-loops at centromeric chromatin contribute to defects in kinetochore integrity and chromosomal instability in budding yeast |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8098821/ https://www.ncbi.nlm.nih.gov/pubmed/33147102 http://dx.doi.org/10.1091/mbc.E20-06-0379 |
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