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Genetic Landscape of Open Chromatin in Yeast
Chromatin regulation underlies a variety of DNA metabolism processes, including transcription, recombination, repair, and replication. To perform a quantitative genetic analysis of chromatin accessibility, we obtained open chromatin profiles across 96 genetically different yeast strains by FAIRE (fo...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3567132/ https://www.ncbi.nlm.nih.gov/pubmed/23408895 http://dx.doi.org/10.1371/journal.pgen.1003229 |
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author | Lee, Kibaick Kim, Sang Cheol Jung, Inkyung Kim, Kwoneel Seo, Jungmin Lee, Heun-Sik Bogu, Gireesh K. Kim, Dongsup Lee, Sanghyuk Lee, Byungwook Choi, Jung Kyoon |
author_facet | Lee, Kibaick Kim, Sang Cheol Jung, Inkyung Kim, Kwoneel Seo, Jungmin Lee, Heun-Sik Bogu, Gireesh K. Kim, Dongsup Lee, Sanghyuk Lee, Byungwook Choi, Jung Kyoon |
author_sort | Lee, Kibaick |
collection | PubMed |
description | Chromatin regulation underlies a variety of DNA metabolism processes, including transcription, recombination, repair, and replication. To perform a quantitative genetic analysis of chromatin accessibility, we obtained open chromatin profiles across 96 genetically different yeast strains by FAIRE (formaldehyde-assisted isolation of regulatory elements) assay followed by sequencing. While 5∼10% of open chromatin region (OCRs) were significantly affected by variations in their underlying DNA sequences, subtelomeric areas as well as gene-rich and gene-poor regions displayed high levels of sequence-independent variation. We performed quantitative trait loci (QTL) mapping using the FAIRE signal for each OCR as a quantitative trait. While individual OCRs were associated with a handful of specific genetic markers, gene expression levels were associated with many regulatory loci. We found multi-target trans-loci responsible for a very large number of OCRs, which seemed to reflect the widespread influence of certain chromatin regulators. Such regulatory hotspots were enriched for known regulatory functions, such as recombinational DNA repair, telomere replication, and general transcription control. The OCRs associated with these multi-target trans-loci coincided with recombination hotspots, telomeres, and gene-rich regions according to the function of the associated regulators. Our findings provide a global quantitative picture of the genetic architecture of chromatin regulation. |
format | Online Article Text |
id | pubmed-3567132 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35671322013-02-13 Genetic Landscape of Open Chromatin in Yeast Lee, Kibaick Kim, Sang Cheol Jung, Inkyung Kim, Kwoneel Seo, Jungmin Lee, Heun-Sik Bogu, Gireesh K. Kim, Dongsup Lee, Sanghyuk Lee, Byungwook Choi, Jung Kyoon PLoS Genet Research Article Chromatin regulation underlies a variety of DNA metabolism processes, including transcription, recombination, repair, and replication. To perform a quantitative genetic analysis of chromatin accessibility, we obtained open chromatin profiles across 96 genetically different yeast strains by FAIRE (formaldehyde-assisted isolation of regulatory elements) assay followed by sequencing. While 5∼10% of open chromatin region (OCRs) were significantly affected by variations in their underlying DNA sequences, subtelomeric areas as well as gene-rich and gene-poor regions displayed high levels of sequence-independent variation. We performed quantitative trait loci (QTL) mapping using the FAIRE signal for each OCR as a quantitative trait. While individual OCRs were associated with a handful of specific genetic markers, gene expression levels were associated with many regulatory loci. We found multi-target trans-loci responsible for a very large number of OCRs, which seemed to reflect the widespread influence of certain chromatin regulators. Such regulatory hotspots were enriched for known regulatory functions, such as recombinational DNA repair, telomere replication, and general transcription control. The OCRs associated with these multi-target trans-loci coincided with recombination hotspots, telomeres, and gene-rich regions according to the function of the associated regulators. Our findings provide a global quantitative picture of the genetic architecture of chromatin regulation. Public Library of Science 2013-02-07 /pmc/articles/PMC3567132/ /pubmed/23408895 http://dx.doi.org/10.1371/journal.pgen.1003229 Text en © 2013 Lee 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Lee, Kibaick Kim, Sang Cheol Jung, Inkyung Kim, Kwoneel Seo, Jungmin Lee, Heun-Sik Bogu, Gireesh K. Kim, Dongsup Lee, Sanghyuk Lee, Byungwook Choi, Jung Kyoon Genetic Landscape of Open Chromatin in Yeast |
title | Genetic Landscape of Open Chromatin in Yeast |
title_full | Genetic Landscape of Open Chromatin in Yeast |
title_fullStr | Genetic Landscape of Open Chromatin in Yeast |
title_full_unstemmed | Genetic Landscape of Open Chromatin in Yeast |
title_short | Genetic Landscape of Open Chromatin in Yeast |
title_sort | genetic landscape of open chromatin in yeast |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3567132/ https://www.ncbi.nlm.nih.gov/pubmed/23408895 http://dx.doi.org/10.1371/journal.pgen.1003229 |
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