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Interferon-Stimulated Gene 15 in the Control of Cellular Responses to Genotoxic Stress

Error-free replication and repair of DNA are pivotal to organisms for faithful transmission of their genetic information. Cells orchestrate complex signaling networks that sense and resolve DNA damage. Post-translational protein modifications by ubiquitin and ubiquitin-like proteins, including SUMO...

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Autores principales: Jeon, Young Joo, Park, Jong Ho, Chung, Chin Ha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Molecular and Cellular Biology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339507/
https://www.ncbi.nlm.nih.gov/pubmed/28241406
http://dx.doi.org/10.14348/molcells.2017.0027
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author Jeon, Young Joo
Park, Jong Ho
Chung, Chin Ha
author_facet Jeon, Young Joo
Park, Jong Ho
Chung, Chin Ha
author_sort Jeon, Young Joo
collection PubMed
description Error-free replication and repair of DNA are pivotal to organisms for faithful transmission of their genetic information. Cells orchestrate complex signaling networks that sense and resolve DNA damage. Post-translational protein modifications by ubiquitin and ubiquitin-like proteins, including SUMO and NEDD8, are critically involved in DNA damage response (DDR) and DNA damage tolerance (DDT). The expression of interferon-stimulated gene 15 (ISG15), the first identified ubiquitin-like protein, has recently been shown to be induced under various DNA damage conditions, such as exposure to UV, camptothecin, and doxorubicin. Here we overview the recent findings on the role of ISG15 and its conjugation to target proteins (e.g., p53, ΔNp63α, and PCNA) in the control of cellular responses to genotoxic stress, such as the inhibition of cell growth and tumorigenesis.
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spelling pubmed-53395072017-03-28 Interferon-Stimulated Gene 15 in the Control of Cellular Responses to Genotoxic Stress Jeon, Young Joo Park, Jong Ho Chung, Chin Ha Mol Cells Minireview Error-free replication and repair of DNA are pivotal to organisms for faithful transmission of their genetic information. Cells orchestrate complex signaling networks that sense and resolve DNA damage. Post-translational protein modifications by ubiquitin and ubiquitin-like proteins, including SUMO and NEDD8, are critically involved in DNA damage response (DDR) and DNA damage tolerance (DDT). The expression of interferon-stimulated gene 15 (ISG15), the first identified ubiquitin-like protein, has recently been shown to be induced under various DNA damage conditions, such as exposure to UV, camptothecin, and doxorubicin. Here we overview the recent findings on the role of ISG15 and its conjugation to target proteins (e.g., p53, ΔNp63α, and PCNA) in the control of cellular responses to genotoxic stress, such as the inhibition of cell growth and tumorigenesis. Korean Society for Molecular and Cellular Biology 2017-02-28 2017-02-27 /pmc/articles/PMC5339507/ /pubmed/28241406 http://dx.doi.org/10.14348/molcells.2017.0027 Text en © The Korean Society for Molecular and Cellular Biology. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/.
spellingShingle Minireview
Jeon, Young Joo
Park, Jong Ho
Chung, Chin Ha
Interferon-Stimulated Gene 15 in the Control of Cellular Responses to Genotoxic Stress
title Interferon-Stimulated Gene 15 in the Control of Cellular Responses to Genotoxic Stress
title_full Interferon-Stimulated Gene 15 in the Control of Cellular Responses to Genotoxic Stress
title_fullStr Interferon-Stimulated Gene 15 in the Control of Cellular Responses to Genotoxic Stress
title_full_unstemmed Interferon-Stimulated Gene 15 in the Control of Cellular Responses to Genotoxic Stress
title_short Interferon-Stimulated Gene 15 in the Control of Cellular Responses to Genotoxic Stress
title_sort interferon-stimulated gene 15 in the control of cellular responses to genotoxic stress
topic Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339507/
https://www.ncbi.nlm.nih.gov/pubmed/28241406
http://dx.doi.org/10.14348/molcells.2017.0027
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