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More than Meets the ISG15: Emerging Roles in the DNA Damage Response and Beyond

Maintenance of genome stability is a crucial priority for any organism. To meet this priority, robust signalling networks exist to facilitate error-free DNA replication and repair. These signalling cascades are subject to various regulatory post-translational modifications that range from simple add...

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Detalles Bibliográficos
Autores principales: Sandy, Zac, da Costa, Isabelle Cristine, Schmidt, Christine K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7698331/
https://www.ncbi.nlm.nih.gov/pubmed/33203188
http://dx.doi.org/10.3390/biom10111557
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author Sandy, Zac
da Costa, Isabelle Cristine
Schmidt, Christine K.
author_facet Sandy, Zac
da Costa, Isabelle Cristine
Schmidt, Christine K.
author_sort Sandy, Zac
collection PubMed
description Maintenance of genome stability is a crucial priority for any organism. To meet this priority, robust signalling networks exist to facilitate error-free DNA replication and repair. These signalling cascades are subject to various regulatory post-translational modifications that range from simple additions of chemical moieties to the conjugation of ubiquitin-like proteins (UBLs). Interferon Stimulated Gene 15 (ISG15) is one such UBL. While classically thought of as a component of antiviral immunity, ISG15 has recently emerged as a regulator of genome stability, with key roles in the DNA damage response (DDR) to modulate p53 signalling and error-free DNA replication. Additional proteomic analyses and cancer-focused studies hint at wider-reaching, uncharacterised functions for ISG15 in genome stability. We review these recent discoveries and highlight future perspectives to increase our understanding of this multifaceted UBL in health and disease.
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spelling pubmed-76983312020-11-29 More than Meets the ISG15: Emerging Roles in the DNA Damage Response and Beyond Sandy, Zac da Costa, Isabelle Cristine Schmidt, Christine K. Biomolecules Review Maintenance of genome stability is a crucial priority for any organism. To meet this priority, robust signalling networks exist to facilitate error-free DNA replication and repair. These signalling cascades are subject to various regulatory post-translational modifications that range from simple additions of chemical moieties to the conjugation of ubiquitin-like proteins (UBLs). Interferon Stimulated Gene 15 (ISG15) is one such UBL. While classically thought of as a component of antiviral immunity, ISG15 has recently emerged as a regulator of genome stability, with key roles in the DNA damage response (DDR) to modulate p53 signalling and error-free DNA replication. Additional proteomic analyses and cancer-focused studies hint at wider-reaching, uncharacterised functions for ISG15 in genome stability. We review these recent discoveries and highlight future perspectives to increase our understanding of this multifaceted UBL in health and disease. MDPI 2020-11-15 /pmc/articles/PMC7698331/ /pubmed/33203188 http://dx.doi.org/10.3390/biom10111557 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Sandy, Zac
da Costa, Isabelle Cristine
Schmidt, Christine K.
More than Meets the ISG15: Emerging Roles in the DNA Damage Response and Beyond
title More than Meets the ISG15: Emerging Roles in the DNA Damage Response and Beyond
title_full More than Meets the ISG15: Emerging Roles in the DNA Damage Response and Beyond
title_fullStr More than Meets the ISG15: Emerging Roles in the DNA Damage Response and Beyond
title_full_unstemmed More than Meets the ISG15: Emerging Roles in the DNA Damage Response and Beyond
title_short More than Meets the ISG15: Emerging Roles in the DNA Damage Response and Beyond
title_sort more than meets the isg15: emerging roles in the dna damage response and beyond
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7698331/
https://www.ncbi.nlm.nih.gov/pubmed/33203188
http://dx.doi.org/10.3390/biom10111557
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