Cargando…

Piecing Together How Peroxiredoxins Maintain Genomic Stability

Peroxiredoxins, a highly conserved family of thiol oxidoreductases, play a key role in oxidant detoxification by partnering with the thioredoxin system to protect against oxidative stress. In addition to their peroxidase activity, certain types of peroxiredoxins possess other biochemical activities,...

Descripción completa

Detalles Bibliográficos
Autores principales: West, James D., Roston, Trevor J., David, Joseph B., Allan, Kristin M., Loberg, Matthew A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316004/
https://www.ncbi.nlm.nih.gov/pubmed/30486489
http://dx.doi.org/10.3390/antiox7120177
_version_ 1783384427501453312
author West, James D.
Roston, Trevor J.
David, Joseph B.
Allan, Kristin M.
Loberg, Matthew A.
author_facet West, James D.
Roston, Trevor J.
David, Joseph B.
Allan, Kristin M.
Loberg, Matthew A.
author_sort West, James D.
collection PubMed
description Peroxiredoxins, a highly conserved family of thiol oxidoreductases, play a key role in oxidant detoxification by partnering with the thioredoxin system to protect against oxidative stress. In addition to their peroxidase activity, certain types of peroxiredoxins possess other biochemical activities, including assistance in preventing protein aggregation upon exposure to high levels of oxidants (molecular chaperone activity), and the transduction of redox signals to downstream proteins (redox switch activity). Mice lacking the peroxiredoxin Prdx1 exhibit an increased incidence of tumor formation, whereas baker’s yeast (Saccharomyces cerevisiae) lacking the orthologous peroxiredoxin Tsa1 exhibit a mutator phenotype. Collectively, these findings suggest a potential link between peroxiredoxins, control of genomic stability, and cancer etiology. Here, we examine the potential mechanisms through which Tsa1 lowers mutation rates, taking into account its diverse biochemical roles in oxidant defense, protein homeostasis, and redox signaling as well as its interplay with thioredoxin and thioredoxin substrates, including ribonucleotide reductase. More work is needed to clarify the nuanced mechanism(s) through which this highly conserved peroxidase influences genome stability, and to determine if this mechanism is similar across a range of species.
format Online
Article
Text
id pubmed-6316004
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-63160042019-01-10 Piecing Together How Peroxiredoxins Maintain Genomic Stability West, James D. Roston, Trevor J. David, Joseph B. Allan, Kristin M. Loberg, Matthew A. Antioxidants (Basel) Review Peroxiredoxins, a highly conserved family of thiol oxidoreductases, play a key role in oxidant detoxification by partnering with the thioredoxin system to protect against oxidative stress. In addition to their peroxidase activity, certain types of peroxiredoxins possess other biochemical activities, including assistance in preventing protein aggregation upon exposure to high levels of oxidants (molecular chaperone activity), and the transduction of redox signals to downstream proteins (redox switch activity). Mice lacking the peroxiredoxin Prdx1 exhibit an increased incidence of tumor formation, whereas baker’s yeast (Saccharomyces cerevisiae) lacking the orthologous peroxiredoxin Tsa1 exhibit a mutator phenotype. Collectively, these findings suggest a potential link between peroxiredoxins, control of genomic stability, and cancer etiology. Here, we examine the potential mechanisms through which Tsa1 lowers mutation rates, taking into account its diverse biochemical roles in oxidant defense, protein homeostasis, and redox signaling as well as its interplay with thioredoxin and thioredoxin substrates, including ribonucleotide reductase. More work is needed to clarify the nuanced mechanism(s) through which this highly conserved peroxidase influences genome stability, and to determine if this mechanism is similar across a range of species. MDPI 2018-11-28 /pmc/articles/PMC6316004/ /pubmed/30486489 http://dx.doi.org/10.3390/antiox7120177 Text en © 2018 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
West, James D.
Roston, Trevor J.
David, Joseph B.
Allan, Kristin M.
Loberg, Matthew A.
Piecing Together How Peroxiredoxins Maintain Genomic Stability
title Piecing Together How Peroxiredoxins Maintain Genomic Stability
title_full Piecing Together How Peroxiredoxins Maintain Genomic Stability
title_fullStr Piecing Together How Peroxiredoxins Maintain Genomic Stability
title_full_unstemmed Piecing Together How Peroxiredoxins Maintain Genomic Stability
title_short Piecing Together How Peroxiredoxins Maintain Genomic Stability
title_sort piecing together how peroxiredoxins maintain genomic stability
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316004/
https://www.ncbi.nlm.nih.gov/pubmed/30486489
http://dx.doi.org/10.3390/antiox7120177
work_keys_str_mv AT westjamesd piecingtogetherhowperoxiredoxinsmaintaingenomicstability
AT rostontrevorj piecingtogetherhowperoxiredoxinsmaintaingenomicstability
AT davidjosephb piecingtogetherhowperoxiredoxinsmaintaingenomicstability
AT allankristinm piecingtogetherhowperoxiredoxinsmaintaingenomicstability
AT lobergmatthewa piecingtogetherhowperoxiredoxinsmaintaingenomicstability