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Monitoring Histone Methylation (H3K9me3) Changes in Live Cells
[Image: see text] H3K9me3 (methylation of lysine 9 of histone H3) is an epigenetic modification that acts as a repressor mark. Several diseases, including cancers and neurological disorders, have been associated with aberrant changes in H3K9me3 levels. Different tools have been developed to enable d...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6705211/ https://www.ncbi.nlm.nih.gov/pubmed/31460452 http://dx.doi.org/10.1021/acsomega.9b01413 |
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author | Sánchez, Oscar F. Mendonca, Agnes Min, Alan Liu, Jichang Yuan, Chongli |
author_facet | Sánchez, Oscar F. Mendonca, Agnes Min, Alan Liu, Jichang Yuan, Chongli |
author_sort | Sánchez, Oscar F. |
collection | PubMed |
description | [Image: see text] H3K9me3 (methylation of lysine 9 of histone H3) is an epigenetic modification that acts as a repressor mark. Several diseases, including cancers and neurological disorders, have been associated with aberrant changes in H3K9me3 levels. Different tools have been developed to enable detection and quantification of H3K9me3 levels in cells. Most techniques, however, lack live cell compatibility. To address this concern, we have engineered recombinant protein sensors for probing H3K9me3 in situ. A heterodimeric sensor containing a chromodomain and chromo shadow domain from HP1a was found to be optimal in recognizing H3K9me3 and exhibited similar spatial resolution to commercial antibodies. Our sensor offers similar quantitative accuracy in characterizing changes in H3K9me3 compared to antibodies but claims single cell resolution. The sensor was applied to evaluate changes in H3K9me3 responding to environmental chemical atrazine (ATZ). ATZ was found to result in significant reductions in H3K9me3 levels after 24 h of exposure. Its impact on the distribution of H3K9me3 among cell populations was also assessed and found to be distinctive. We foresee the application of our sensors in multiple toxicity and drug-screening applications. |
format | Online Article Text |
id | pubmed-6705211 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-67052112019-08-27 Monitoring Histone Methylation (H3K9me3) Changes in Live Cells Sánchez, Oscar F. Mendonca, Agnes Min, Alan Liu, Jichang Yuan, Chongli ACS Omega [Image: see text] H3K9me3 (methylation of lysine 9 of histone H3) is an epigenetic modification that acts as a repressor mark. Several diseases, including cancers and neurological disorders, have been associated with aberrant changes in H3K9me3 levels. Different tools have been developed to enable detection and quantification of H3K9me3 levels in cells. Most techniques, however, lack live cell compatibility. To address this concern, we have engineered recombinant protein sensors for probing H3K9me3 in situ. A heterodimeric sensor containing a chromodomain and chromo shadow domain from HP1a was found to be optimal in recognizing H3K9me3 and exhibited similar spatial resolution to commercial antibodies. Our sensor offers similar quantitative accuracy in characterizing changes in H3K9me3 compared to antibodies but claims single cell resolution. The sensor was applied to evaluate changes in H3K9me3 responding to environmental chemical atrazine (ATZ). ATZ was found to result in significant reductions in H3K9me3 levels after 24 h of exposure. Its impact on the distribution of H3K9me3 among cell populations was also assessed and found to be distinctive. We foresee the application of our sensors in multiple toxicity and drug-screening applications. American Chemical Society 2019-08-01 /pmc/articles/PMC6705211/ /pubmed/31460452 http://dx.doi.org/10.1021/acsomega.9b01413 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Sánchez, Oscar F. Mendonca, Agnes Min, Alan Liu, Jichang Yuan, Chongli Monitoring Histone Methylation (H3K9me3) Changes in Live Cells |
title | Monitoring Histone Methylation (H3K9me3) Changes in
Live Cells |
title_full | Monitoring Histone Methylation (H3K9me3) Changes in
Live Cells |
title_fullStr | Monitoring Histone Methylation (H3K9me3) Changes in
Live Cells |
title_full_unstemmed | Monitoring Histone Methylation (H3K9me3) Changes in
Live Cells |
title_short | Monitoring Histone Methylation (H3K9me3) Changes in
Live Cells |
title_sort | monitoring histone methylation (h3k9me3) changes in
live cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6705211/ https://www.ncbi.nlm.nih.gov/pubmed/31460452 http://dx.doi.org/10.1021/acsomega.9b01413 |
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