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Analysis of DNA double-strand break response and chromatin structure in mitosis using laser microirradiation

In this study the femtosecond near-IR and nanosecond green lasers are used to induce alterations in mitotic chromosomes. The subsequent double-strand break responses are studied. We show that both lasers are capable of creating comparable chromosomal alterations and that a phase paling observed with...

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Autores principales: Gomez-Godinez, Veronica, Wu, Tao, Sherman, Adria J., Lee, Christopher S., Liaw, Lih-Huei, Zhongsheng, You, Yokomori, Kyoko, Berns, Michael W.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001094/
https://www.ncbi.nlm.nih.gov/pubmed/20923785
http://dx.doi.org/10.1093/nar/gkq836
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author Gomez-Godinez, Veronica
Wu, Tao
Sherman, Adria J.
Lee, Christopher S.
Liaw, Lih-Huei
Zhongsheng, You
Yokomori, Kyoko
Berns, Michael W.
author_facet Gomez-Godinez, Veronica
Wu, Tao
Sherman, Adria J.
Lee, Christopher S.
Liaw, Lih-Huei
Zhongsheng, You
Yokomori, Kyoko
Berns, Michael W.
author_sort Gomez-Godinez, Veronica
collection PubMed
description In this study the femtosecond near-IR and nanosecond green lasers are used to induce alterations in mitotic chromosomes. The subsequent double-strand break responses are studied. We show that both lasers are capable of creating comparable chromosomal alterations and that a phase paling observed within 1–2 s of laser exposure is associated with an alteration of chromatin as confirmed by serial section electron microscopy, DAPI, γH2AX and phospho-H3 staining. Additionally, the accumulation of dark material observed using phase contrast light microscopy (indicative of a change in refractive index of the chromatin) ∼34 s post-laser exposure corresponds spatially to the accumulation of Nbs1, Ku and ubiquitin. This study demonstrates that chromosomes selectively altered in mitosis initiate the DNA damage response within 30 s and that the accumulation of proteins are visually represented by phase-dark material at the irradiation site, allowing us to determine the fate of the damage as cells enter G1. These results occur with two widely different laser systems, making this approach to study DNA damage responses in the mitotic phase generally available to many different labs. Additionally, we present a summary of most of the published laser studies on chromosomes in order to provide a general guide of the lasers and operating parameters used by other laboratories.
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spelling pubmed-30010942010-12-13 Analysis of DNA double-strand break response and chromatin structure in mitosis using laser microirradiation Gomez-Godinez, Veronica Wu, Tao Sherman, Adria J. Lee, Christopher S. Liaw, Lih-Huei Zhongsheng, You Yokomori, Kyoko Berns, Michael W. Nucleic Acids Res Methods Online In this study the femtosecond near-IR and nanosecond green lasers are used to induce alterations in mitotic chromosomes. The subsequent double-strand break responses are studied. We show that both lasers are capable of creating comparable chromosomal alterations and that a phase paling observed within 1–2 s of laser exposure is associated with an alteration of chromatin as confirmed by serial section electron microscopy, DAPI, γH2AX and phospho-H3 staining. Additionally, the accumulation of dark material observed using phase contrast light microscopy (indicative of a change in refractive index of the chromatin) ∼34 s post-laser exposure corresponds spatially to the accumulation of Nbs1, Ku and ubiquitin. This study demonstrates that chromosomes selectively altered in mitosis initiate the DNA damage response within 30 s and that the accumulation of proteins are visually represented by phase-dark material at the irradiation site, allowing us to determine the fate of the damage as cells enter G1. These results occur with two widely different laser systems, making this approach to study DNA damage responses in the mitotic phase generally available to many different labs. Additionally, we present a summary of most of the published laser studies on chromosomes in order to provide a general guide of the lasers and operating parameters used by other laboratories. Oxford University Press 2010-12 2010-10-04 /pmc/articles/PMC3001094/ /pubmed/20923785 http://dx.doi.org/10.1093/nar/gkq836 Text en © The Author(s) 2010. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods Online
Gomez-Godinez, Veronica
Wu, Tao
Sherman, Adria J.
Lee, Christopher S.
Liaw, Lih-Huei
Zhongsheng, You
Yokomori, Kyoko
Berns, Michael W.
Analysis of DNA double-strand break response and chromatin structure in mitosis using laser microirradiation
title Analysis of DNA double-strand break response and chromatin structure in mitosis using laser microirradiation
title_full Analysis of DNA double-strand break response and chromatin structure in mitosis using laser microirradiation
title_fullStr Analysis of DNA double-strand break response and chromatin structure in mitosis using laser microirradiation
title_full_unstemmed Analysis of DNA double-strand break response and chromatin structure in mitosis using laser microirradiation
title_short Analysis of DNA double-strand break response and chromatin structure in mitosis using laser microirradiation
title_sort analysis of dna double-strand break response and chromatin structure in mitosis using laser microirradiation
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001094/
https://www.ncbi.nlm.nih.gov/pubmed/20923785
http://dx.doi.org/10.1093/nar/gkq836
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