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The DNA damage checkpoint: A tale from budding yeast

Studies performed in the yeasts Saccharomyces cerevisiae and Schizosaccharomyces pombe have led the way in defining the DNA damage checkpoint and in identifying most of the proteins involved in this regulatory network, which turned out to have structural and functional equivalents in humans. Subsequ...

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Autores principales: Pizzul, Paolo, Casari, Erika, Gnugnoli, Marco, Rinaldi, Carlo, Corallo, Flavio, Longhese, Maria Pia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520983/
https://www.ncbi.nlm.nih.gov/pubmed/36186482
http://dx.doi.org/10.3389/fgene.2022.995163
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author Pizzul, Paolo
Casari, Erika
Gnugnoli, Marco
Rinaldi, Carlo
Corallo, Flavio
Longhese, Maria Pia
author_facet Pizzul, Paolo
Casari, Erika
Gnugnoli, Marco
Rinaldi, Carlo
Corallo, Flavio
Longhese, Maria Pia
author_sort Pizzul, Paolo
collection PubMed
description Studies performed in the yeasts Saccharomyces cerevisiae and Schizosaccharomyces pombe have led the way in defining the DNA damage checkpoint and in identifying most of the proteins involved in this regulatory network, which turned out to have structural and functional equivalents in humans. Subsequent experiments revealed that the checkpoint is an elaborate signal transduction pathway that has the ability to sense and signal the presence of damaged DNA and transduce this information to influence a multifaceted cellular response that is essential for cancer avoidance. This review focuses on the work that was done in Saccharomyces cerevisiae to articulate the checkpoint concept, to identify its players and the mechanisms of activation and deactivation.
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spelling pubmed-95209832022-09-30 The DNA damage checkpoint: A tale from budding yeast Pizzul, Paolo Casari, Erika Gnugnoli, Marco Rinaldi, Carlo Corallo, Flavio Longhese, Maria Pia Front Genet Genetics Studies performed in the yeasts Saccharomyces cerevisiae and Schizosaccharomyces pombe have led the way in defining the DNA damage checkpoint and in identifying most of the proteins involved in this regulatory network, which turned out to have structural and functional equivalents in humans. Subsequent experiments revealed that the checkpoint is an elaborate signal transduction pathway that has the ability to sense and signal the presence of damaged DNA and transduce this information to influence a multifaceted cellular response that is essential for cancer avoidance. This review focuses on the work that was done in Saccharomyces cerevisiae to articulate the checkpoint concept, to identify its players and the mechanisms of activation and deactivation. Frontiers Media S.A. 2022-09-15 /pmc/articles/PMC9520983/ /pubmed/36186482 http://dx.doi.org/10.3389/fgene.2022.995163 Text en Copyright © 2022 Pizzul, Casari, Gnugnoli, Rinaldi, Corallo and Longhese. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Pizzul, Paolo
Casari, Erika
Gnugnoli, Marco
Rinaldi, Carlo
Corallo, Flavio
Longhese, Maria Pia
The DNA damage checkpoint: A tale from budding yeast
title The DNA damage checkpoint: A tale from budding yeast
title_full The DNA damage checkpoint: A tale from budding yeast
title_fullStr The DNA damage checkpoint: A tale from budding yeast
title_full_unstemmed The DNA damage checkpoint: A tale from budding yeast
title_short The DNA damage checkpoint: A tale from budding yeast
title_sort dna damage checkpoint: a tale from budding yeast
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520983/
https://www.ncbi.nlm.nih.gov/pubmed/36186482
http://dx.doi.org/10.3389/fgene.2022.995163
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