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WDR76 Co-Localizes with Heterochromatin Related Proteins and Rapidly Responds to DNA Damage
Proteins that respond to DNA damage play critical roles in normal and diseased states in human biology. Studies have suggested that the S. cerevisiae protein CMR1/YDL156w is associated with histones and is possibly associated with DNA repair and replication processes. Through a quantitative proteomi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4889050/ https://www.ncbi.nlm.nih.gov/pubmed/27248496 http://dx.doi.org/10.1371/journal.pone.0155492 |
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author | Gilmore, Joshua M. Sardiu, Mihaela E. Groppe, Brad D. Thornton, Janet L. Liu, Xingyu Dayebgadoh, Gerald Banks, Charles A. Slaughter, Brian D. Unruh, Jay R. Workman, Jerry L. Florens, Laurence Washburn, Michael P. |
author_facet | Gilmore, Joshua M. Sardiu, Mihaela E. Groppe, Brad D. Thornton, Janet L. Liu, Xingyu Dayebgadoh, Gerald Banks, Charles A. Slaughter, Brian D. Unruh, Jay R. Workman, Jerry L. Florens, Laurence Washburn, Michael P. |
author_sort | Gilmore, Joshua M. |
collection | PubMed |
description | Proteins that respond to DNA damage play critical roles in normal and diseased states in human biology. Studies have suggested that the S. cerevisiae protein CMR1/YDL156w is associated with histones and is possibly associated with DNA repair and replication processes. Through a quantitative proteomic analysis of affinity purifications here we show that the human homologue of this protein, WDR76, shares multiple protein associations with the histones H2A, H2B, and H4. Furthermore, our quantitative proteomic analysis of WDR76 associated proteins demonstrated links to proteins in the DNA damage response like PARP1 and XRCC5 and heterochromatin related proteins like CBX1, CBX3, and CBX5. Co-immunoprecipitation studies validated these interactions. Next, quantitative imaging studies demonstrated that WDR76 was recruited to laser induced DNA damage immediately after induction, and we compared the recruitment of WDR76 to laser induced DNA damage to known DNA damage proteins like PARP1, XRCC5, and RPA1. In addition, WDR76 co-localizes to puncta with the heterochromatin proteins CBX1 and CBX5, which are also recruited to DNA damage but much less intensely than WDR76. This work demonstrates the chromatin and DNA damage protein associations of WDR76 and demonstrates the rapid response of WDR76 to laser induced DNA damage. |
format | Online Article Text |
id | pubmed-4889050 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-48890502016-06-10 WDR76 Co-Localizes with Heterochromatin Related Proteins and Rapidly Responds to DNA Damage Gilmore, Joshua M. Sardiu, Mihaela E. Groppe, Brad D. Thornton, Janet L. Liu, Xingyu Dayebgadoh, Gerald Banks, Charles A. Slaughter, Brian D. Unruh, Jay R. Workman, Jerry L. Florens, Laurence Washburn, Michael P. PLoS One Research Article Proteins that respond to DNA damage play critical roles in normal and diseased states in human biology. Studies have suggested that the S. cerevisiae protein CMR1/YDL156w is associated with histones and is possibly associated with DNA repair and replication processes. Through a quantitative proteomic analysis of affinity purifications here we show that the human homologue of this protein, WDR76, shares multiple protein associations with the histones H2A, H2B, and H4. Furthermore, our quantitative proteomic analysis of WDR76 associated proteins demonstrated links to proteins in the DNA damage response like PARP1 and XRCC5 and heterochromatin related proteins like CBX1, CBX3, and CBX5. Co-immunoprecipitation studies validated these interactions. Next, quantitative imaging studies demonstrated that WDR76 was recruited to laser induced DNA damage immediately after induction, and we compared the recruitment of WDR76 to laser induced DNA damage to known DNA damage proteins like PARP1, XRCC5, and RPA1. In addition, WDR76 co-localizes to puncta with the heterochromatin proteins CBX1 and CBX5, which are also recruited to DNA damage but much less intensely than WDR76. This work demonstrates the chromatin and DNA damage protein associations of WDR76 and demonstrates the rapid response of WDR76 to laser induced DNA damage. Public Library of Science 2016-06-01 /pmc/articles/PMC4889050/ /pubmed/27248496 http://dx.doi.org/10.1371/journal.pone.0155492 Text en © 2016 Gilmore 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 Gilmore, Joshua M. Sardiu, Mihaela E. Groppe, Brad D. Thornton, Janet L. Liu, Xingyu Dayebgadoh, Gerald Banks, Charles A. Slaughter, Brian D. Unruh, Jay R. Workman, Jerry L. Florens, Laurence Washburn, Michael P. WDR76 Co-Localizes with Heterochromatin Related Proteins and Rapidly Responds to DNA Damage |
title | WDR76 Co-Localizes with Heterochromatin Related Proteins and Rapidly Responds to DNA Damage |
title_full | WDR76 Co-Localizes with Heterochromatin Related Proteins and Rapidly Responds to DNA Damage |
title_fullStr | WDR76 Co-Localizes with Heterochromatin Related Proteins and Rapidly Responds to DNA Damage |
title_full_unstemmed | WDR76 Co-Localizes with Heterochromatin Related Proteins and Rapidly Responds to DNA Damage |
title_short | WDR76 Co-Localizes with Heterochromatin Related Proteins and Rapidly Responds to DNA Damage |
title_sort | wdr76 co-localizes with heterochromatin related proteins and rapidly responds to dna damage |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4889050/ https://www.ncbi.nlm.nih.gov/pubmed/27248496 http://dx.doi.org/10.1371/journal.pone.0155492 |
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