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Condensation of Ded1p Promotes a Translational Switch from Housekeeping to Stress Protein Production

Cells sense elevated temperatures and mount an adaptive heat shock response that involves changes in gene expression, but the underlying mechanisms, particularly on the level of translation, remain unknown. Here we report that, in budding yeast, the essential translation initiation factor Ded1p unde...

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Autores principales: Iserman, Christiane, Desroches Altamirano, Christine, Jegers, Ceciel, Friedrich, Ulrike, Zarin, Taraneh, Fritsch, Anatol W., Mittasch, Matthäus, Domingues, Antonio, Hersemann, Lena, Jahnel, Marcus, Richter, Doris, Guenther, Ulf-Peter, Hentze, Matthias W., Moses, Alan M., Hyman, Anthony A., Kramer, Günter, Kreysing, Moritz, Franzmann, Titus M., Alberti, Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7237889/
https://www.ncbi.nlm.nih.gov/pubmed/32359423
http://dx.doi.org/10.1016/j.cell.2020.04.009
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author Iserman, Christiane
Desroches Altamirano, Christine
Jegers, Ceciel
Friedrich, Ulrike
Zarin, Taraneh
Fritsch, Anatol W.
Mittasch, Matthäus
Domingues, Antonio
Hersemann, Lena
Jahnel, Marcus
Richter, Doris
Guenther, Ulf-Peter
Hentze, Matthias W.
Moses, Alan M.
Hyman, Anthony A.
Kramer, Günter
Kreysing, Moritz
Franzmann, Titus M.
Alberti, Simon
author_facet Iserman, Christiane
Desroches Altamirano, Christine
Jegers, Ceciel
Friedrich, Ulrike
Zarin, Taraneh
Fritsch, Anatol W.
Mittasch, Matthäus
Domingues, Antonio
Hersemann, Lena
Jahnel, Marcus
Richter, Doris
Guenther, Ulf-Peter
Hentze, Matthias W.
Moses, Alan M.
Hyman, Anthony A.
Kramer, Günter
Kreysing, Moritz
Franzmann, Titus M.
Alberti, Simon
author_sort Iserman, Christiane
collection PubMed
description Cells sense elevated temperatures and mount an adaptive heat shock response that involves changes in gene expression, but the underlying mechanisms, particularly on the level of translation, remain unknown. Here we report that, in budding yeast, the essential translation initiation factor Ded1p undergoes heat-induced phase separation into gel-like condensates. Using ribosome profiling and an in vitro translation assay, we reveal that condensate formation inactivates Ded1p and represses translation of housekeeping mRNAs while promoting translation of stress mRNAs. Testing a variant of Ded1p with altered phase behavior as well as Ded1p homologs from diverse species, we demonstrate that Ded1p condensation is adaptive and fine-tuned to the maximum growth temperature of the respective organism. We conclude that Ded1p condensation is an integral part of an extended heat shock response that selectively represses translation of housekeeping mRNAs to promote survival under conditions of severe heat stress.
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spelling pubmed-72378892020-05-26 Condensation of Ded1p Promotes a Translational Switch from Housekeeping to Stress Protein Production Iserman, Christiane Desroches Altamirano, Christine Jegers, Ceciel Friedrich, Ulrike Zarin, Taraneh Fritsch, Anatol W. Mittasch, Matthäus Domingues, Antonio Hersemann, Lena Jahnel, Marcus Richter, Doris Guenther, Ulf-Peter Hentze, Matthias W. Moses, Alan M. Hyman, Anthony A. Kramer, Günter Kreysing, Moritz Franzmann, Titus M. Alberti, Simon Cell Article Cells sense elevated temperatures and mount an adaptive heat shock response that involves changes in gene expression, but the underlying mechanisms, particularly on the level of translation, remain unknown. Here we report that, in budding yeast, the essential translation initiation factor Ded1p undergoes heat-induced phase separation into gel-like condensates. Using ribosome profiling and an in vitro translation assay, we reveal that condensate formation inactivates Ded1p and represses translation of housekeeping mRNAs while promoting translation of stress mRNAs. Testing a variant of Ded1p with altered phase behavior as well as Ded1p homologs from diverse species, we demonstrate that Ded1p condensation is adaptive and fine-tuned to the maximum growth temperature of the respective organism. We conclude that Ded1p condensation is an integral part of an extended heat shock response that selectively represses translation of housekeeping mRNAs to promote survival under conditions of severe heat stress. Cell Press 2020-05-14 /pmc/articles/PMC7237889/ /pubmed/32359423 http://dx.doi.org/10.1016/j.cell.2020.04.009 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Iserman, Christiane
Desroches Altamirano, Christine
Jegers, Ceciel
Friedrich, Ulrike
Zarin, Taraneh
Fritsch, Anatol W.
Mittasch, Matthäus
Domingues, Antonio
Hersemann, Lena
Jahnel, Marcus
Richter, Doris
Guenther, Ulf-Peter
Hentze, Matthias W.
Moses, Alan M.
Hyman, Anthony A.
Kramer, Günter
Kreysing, Moritz
Franzmann, Titus M.
Alberti, Simon
Condensation of Ded1p Promotes a Translational Switch from Housekeeping to Stress Protein Production
title Condensation of Ded1p Promotes a Translational Switch from Housekeeping to Stress Protein Production
title_full Condensation of Ded1p Promotes a Translational Switch from Housekeeping to Stress Protein Production
title_fullStr Condensation of Ded1p Promotes a Translational Switch from Housekeeping to Stress Protein Production
title_full_unstemmed Condensation of Ded1p Promotes a Translational Switch from Housekeeping to Stress Protein Production
title_short Condensation of Ded1p Promotes a Translational Switch from Housekeeping to Stress Protein Production
title_sort condensation of ded1p promotes a translational switch from housekeeping to stress protein production
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7237889/
https://www.ncbi.nlm.nih.gov/pubmed/32359423
http://dx.doi.org/10.1016/j.cell.2020.04.009
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