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Protein kinase A controls yeast growth in visible light

BACKGROUND: A wide variety of photosynthetic and non-photosynthetic species sense and respond to light, having developed protective mechanisms to adapt to damaging effects on DNA and proteins. While the biology of UV light-induced damage has been well studied, cellular responses to stress from visib...

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Autores principales: Molin, Mikael, Logg, Katarina, Bodvard, Kristofer, Peeters, Ken, Forsmark, Annabelle, Roger, Friederike, Jörhov, Anna, Mishra, Neha, Billod, Jean-Marc, Amir, Sabiha, Andersson, Mikael, Eriksson, Leif A., Warringer, Jonas, Käll, Mikael, Blomberg, Anders
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667738/
https://www.ncbi.nlm.nih.gov/pubmed/33198745
http://dx.doi.org/10.1186/s12915-020-00867-4
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author Molin, Mikael
Logg, Katarina
Bodvard, Kristofer
Peeters, Ken
Forsmark, Annabelle
Roger, Friederike
Jörhov, Anna
Mishra, Neha
Billod, Jean-Marc
Amir, Sabiha
Andersson, Mikael
Eriksson, Leif A.
Warringer, Jonas
Käll, Mikael
Blomberg, Anders
author_facet Molin, Mikael
Logg, Katarina
Bodvard, Kristofer
Peeters, Ken
Forsmark, Annabelle
Roger, Friederike
Jörhov, Anna
Mishra, Neha
Billod, Jean-Marc
Amir, Sabiha
Andersson, Mikael
Eriksson, Leif A.
Warringer, Jonas
Käll, Mikael
Blomberg, Anders
author_sort Molin, Mikael
collection PubMed
description BACKGROUND: A wide variety of photosynthetic and non-photosynthetic species sense and respond to light, having developed protective mechanisms to adapt to damaging effects on DNA and proteins. While the biology of UV light-induced damage has been well studied, cellular responses to stress from visible light (400–700 nm) remain poorly understood despite being a regular part of the life cycle of many organisms. Here, we developed a high-throughput method for measuring growth under visible light stress and used it to screen for light sensitivity in the yeast gene deletion collection. RESULTS: We found genes involved in HOG pathway signaling, RNA polymerase II transcription, translation, diphthamide modifications of the translational elongation factor eEF2, and the oxidative stress response to be required for light resistance. Reduced nuclear localization of the transcription factor Msn2 and lower glycogen accumulation indicated higher protein kinase A (cAMP-dependent protein kinase, PKA) activity in many light-sensitive gene deletion strains. We therefore used an ectopic fluorescent PKA reporter and mutants with constitutively altered PKA activity to show that repression of PKA is essential for resistance to visible light. CONCLUSION: We conclude that yeast photobiology is multifaceted and that protein kinase A plays a key role in the ability of cells to grow upon visible light exposure. We propose that visible light impacts on the biology and evolution of many non-photosynthetic organisms and have practical implications for how organisms are studied in the laboratory, with or without illumination.
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spelling pubmed-76677382020-11-17 Protein kinase A controls yeast growth in visible light Molin, Mikael Logg, Katarina Bodvard, Kristofer Peeters, Ken Forsmark, Annabelle Roger, Friederike Jörhov, Anna Mishra, Neha Billod, Jean-Marc Amir, Sabiha Andersson, Mikael Eriksson, Leif A. Warringer, Jonas Käll, Mikael Blomberg, Anders BMC Biol Research Article BACKGROUND: A wide variety of photosynthetic and non-photosynthetic species sense and respond to light, having developed protective mechanisms to adapt to damaging effects on DNA and proteins. While the biology of UV light-induced damage has been well studied, cellular responses to stress from visible light (400–700 nm) remain poorly understood despite being a regular part of the life cycle of many organisms. Here, we developed a high-throughput method for measuring growth under visible light stress and used it to screen for light sensitivity in the yeast gene deletion collection. RESULTS: We found genes involved in HOG pathway signaling, RNA polymerase II transcription, translation, diphthamide modifications of the translational elongation factor eEF2, and the oxidative stress response to be required for light resistance. Reduced nuclear localization of the transcription factor Msn2 and lower glycogen accumulation indicated higher protein kinase A (cAMP-dependent protein kinase, PKA) activity in many light-sensitive gene deletion strains. We therefore used an ectopic fluorescent PKA reporter and mutants with constitutively altered PKA activity to show that repression of PKA is essential for resistance to visible light. CONCLUSION: We conclude that yeast photobiology is multifaceted and that protein kinase A plays a key role in the ability of cells to grow upon visible light exposure. We propose that visible light impacts on the biology and evolution of many non-photosynthetic organisms and have practical implications for how organisms are studied in the laboratory, with or without illumination. BioMed Central 2020-11-16 /pmc/articles/PMC7667738/ /pubmed/33198745 http://dx.doi.org/10.1186/s12915-020-00867-4 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Molin, Mikael
Logg, Katarina
Bodvard, Kristofer
Peeters, Ken
Forsmark, Annabelle
Roger, Friederike
Jörhov, Anna
Mishra, Neha
Billod, Jean-Marc
Amir, Sabiha
Andersson, Mikael
Eriksson, Leif A.
Warringer, Jonas
Käll, Mikael
Blomberg, Anders
Protein kinase A controls yeast growth in visible light
title Protein kinase A controls yeast growth in visible light
title_full Protein kinase A controls yeast growth in visible light
title_fullStr Protein kinase A controls yeast growth in visible light
title_full_unstemmed Protein kinase A controls yeast growth in visible light
title_short Protein kinase A controls yeast growth in visible light
title_sort protein kinase a controls yeast growth in visible light
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667738/
https://www.ncbi.nlm.nih.gov/pubmed/33198745
http://dx.doi.org/10.1186/s12915-020-00867-4
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