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Evolutionary Divergence in DNA Damage Responses among Fungi

Cell cycle checkpoints and DNA repair pathways contribute to maintaining genome integrity and are thought to be evolutionarily ancient and broadly conserved. For example, in the yeast Saccharomyces cerevisiae and humans, DNA damage induces activation of a checkpoint effector kinase, Rad53p (human ho...

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Autor principal: Steenwyk, Jacob L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092291/
https://www.ncbi.nlm.nih.gov/pubmed/33727357
http://dx.doi.org/10.1128/mBio.03348-20
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author Steenwyk, Jacob L.
author_facet Steenwyk, Jacob L.
author_sort Steenwyk, Jacob L.
collection PubMed
description Cell cycle checkpoints and DNA repair pathways contribute to maintaining genome integrity and are thought to be evolutionarily ancient and broadly conserved. For example, in the yeast Saccharomyces cerevisiae and humans, DNA damage induces activation of a checkpoint effector kinase, Rad53p (human homolog Chk2), to promote cell cycle arrest and transcription of DNA repair genes. However, recent studies have revealed variation in the DNA damage response networks of some fungi. For example, Shor et al. (mBio 11:e03044-20, 2020, https://doi.org/10.1128/mBio.03044-20) demonstrate that in comparison to S. cerevisiae, the fungal pathogen Candida glabrata has reduced activation of Rad53p in response to DNA damage. Consequently, some downstream targets that contribute to S. cerevisiae genome maintenance, such as DNA polymerases, are transcriptionally downregulated in C. glabrata. Downregulation of genome maintenance genes likely contributes to higher rates of mitotic failure and cell death in C. glabrata. This and other recent findings highlight evolutionary diversity in eukaryotic DNA damage responses.
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spelling pubmed-80922912021-05-04 Evolutionary Divergence in DNA Damage Responses among Fungi Steenwyk, Jacob L. mBio Commentary Cell cycle checkpoints and DNA repair pathways contribute to maintaining genome integrity and are thought to be evolutionarily ancient and broadly conserved. For example, in the yeast Saccharomyces cerevisiae and humans, DNA damage induces activation of a checkpoint effector kinase, Rad53p (human homolog Chk2), to promote cell cycle arrest and transcription of DNA repair genes. However, recent studies have revealed variation in the DNA damage response networks of some fungi. For example, Shor et al. (mBio 11:e03044-20, 2020, https://doi.org/10.1128/mBio.03044-20) demonstrate that in comparison to S. cerevisiae, the fungal pathogen Candida glabrata has reduced activation of Rad53p in response to DNA damage. Consequently, some downstream targets that contribute to S. cerevisiae genome maintenance, such as DNA polymerases, are transcriptionally downregulated in C. glabrata. Downregulation of genome maintenance genes likely contributes to higher rates of mitotic failure and cell death in C. glabrata. This and other recent findings highlight evolutionary diversity in eukaryotic DNA damage responses. American Society for Microbiology 2021-03-16 /pmc/articles/PMC8092291/ /pubmed/33727357 http://dx.doi.org/10.1128/mBio.03348-20 Text en Copyright © 2021 Steenwyk. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Commentary
Steenwyk, Jacob L.
Evolutionary Divergence in DNA Damage Responses among Fungi
title Evolutionary Divergence in DNA Damage Responses among Fungi
title_full Evolutionary Divergence in DNA Damage Responses among Fungi
title_fullStr Evolutionary Divergence in DNA Damage Responses among Fungi
title_full_unstemmed Evolutionary Divergence in DNA Damage Responses among Fungi
title_short Evolutionary Divergence in DNA Damage Responses among Fungi
title_sort evolutionary divergence in dna damage responses among fungi
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092291/
https://www.ncbi.nlm.nih.gov/pubmed/33727357
http://dx.doi.org/10.1128/mBio.03348-20
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