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Arabidopsis REI-LIKE proteins activate ribosome biogenesis during cold acclimation

Arabidopsis REIL proteins are cytosolic ribosomal 60S-biogenesis factors. After shift to 10 °C, reil mutants deplete and slowly replenish non-translating eukaryotic ribosome complexes of root tissue, while controlling the balance of non-translating 40S- and 60S-subunits. Reil mutations respond by hy...

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Autores principales: Cheong, Bo Eng, Beine-Golovchuk, Olga, Gorka, Michal, Ho, William Wing Ho, Martinez-Seidel, Federico, Firmino, Alexandre Augusto Pereira, Skirycz, Aleksandra, Roessner, Ute, Kopka, Joachim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844247/
https://www.ncbi.nlm.nih.gov/pubmed/33510206
http://dx.doi.org/10.1038/s41598-021-81610-z
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author Cheong, Bo Eng
Beine-Golovchuk, Olga
Gorka, Michal
Ho, William Wing Ho
Martinez-Seidel, Federico
Firmino, Alexandre Augusto Pereira
Skirycz, Aleksandra
Roessner, Ute
Kopka, Joachim
author_facet Cheong, Bo Eng
Beine-Golovchuk, Olga
Gorka, Michal
Ho, William Wing Ho
Martinez-Seidel, Federico
Firmino, Alexandre Augusto Pereira
Skirycz, Aleksandra
Roessner, Ute
Kopka, Joachim
author_sort Cheong, Bo Eng
collection PubMed
description Arabidopsis REIL proteins are cytosolic ribosomal 60S-biogenesis factors. After shift to 10 °C, reil mutants deplete and slowly replenish non-translating eukaryotic ribosome complexes of root tissue, while controlling the balance of non-translating 40S- and 60S-subunits. Reil mutations respond by hyper-accumulation of non-translating subunits at steady-state temperature; after cold-shift, a KCl-sensitive 80S sub-fraction remains depleted. We infer that Arabidopsis may buffer fluctuating translation by pre-existing non-translating ribosomes before de novo synthesis meets temperature-induced demands. Reil1 reil2 double mutants accumulate 43S-preinitiation and pre-60S-maturation complexes and alter paralog composition of ribosomal proteins in non-translating complexes. With few exceptions, e.g. RPL3B and RPL24C, these changes are not under transcriptional control. Our study suggests requirement of de novo synthesis of eukaryotic ribosomes for long-term cold acclimation, feedback control of NUC2 and eIF3C2 transcription and links new proteins, AT1G03250, AT5G60530, to plant ribosome biogenesis. We propose that Arabidopsis requires biosynthesis of specialized ribosomes for cold acclimation.
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spelling pubmed-78442472021-02-01 Arabidopsis REI-LIKE proteins activate ribosome biogenesis during cold acclimation Cheong, Bo Eng Beine-Golovchuk, Olga Gorka, Michal Ho, William Wing Ho Martinez-Seidel, Federico Firmino, Alexandre Augusto Pereira Skirycz, Aleksandra Roessner, Ute Kopka, Joachim Sci Rep Article Arabidopsis REIL proteins are cytosolic ribosomal 60S-biogenesis factors. After shift to 10 °C, reil mutants deplete and slowly replenish non-translating eukaryotic ribosome complexes of root tissue, while controlling the balance of non-translating 40S- and 60S-subunits. Reil mutations respond by hyper-accumulation of non-translating subunits at steady-state temperature; after cold-shift, a KCl-sensitive 80S sub-fraction remains depleted. We infer that Arabidopsis may buffer fluctuating translation by pre-existing non-translating ribosomes before de novo synthesis meets temperature-induced demands. Reil1 reil2 double mutants accumulate 43S-preinitiation and pre-60S-maturation complexes and alter paralog composition of ribosomal proteins in non-translating complexes. With few exceptions, e.g. RPL3B and RPL24C, these changes are not under transcriptional control. Our study suggests requirement of de novo synthesis of eukaryotic ribosomes for long-term cold acclimation, feedback control of NUC2 and eIF3C2 transcription and links new proteins, AT1G03250, AT5G60530, to plant ribosome biogenesis. We propose that Arabidopsis requires biosynthesis of specialized ribosomes for cold acclimation. Nature Publishing Group UK 2021-01-28 /pmc/articles/PMC7844247/ /pubmed/33510206 http://dx.doi.org/10.1038/s41598-021-81610-z Text en © The Author(s) 2021 Open Access This 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/.
spellingShingle Article
Cheong, Bo Eng
Beine-Golovchuk, Olga
Gorka, Michal
Ho, William Wing Ho
Martinez-Seidel, Federico
Firmino, Alexandre Augusto Pereira
Skirycz, Aleksandra
Roessner, Ute
Kopka, Joachim
Arabidopsis REI-LIKE proteins activate ribosome biogenesis during cold acclimation
title Arabidopsis REI-LIKE proteins activate ribosome biogenesis during cold acclimation
title_full Arabidopsis REI-LIKE proteins activate ribosome biogenesis during cold acclimation
title_fullStr Arabidopsis REI-LIKE proteins activate ribosome biogenesis during cold acclimation
title_full_unstemmed Arabidopsis REI-LIKE proteins activate ribosome biogenesis during cold acclimation
title_short Arabidopsis REI-LIKE proteins activate ribosome biogenesis during cold acclimation
title_sort arabidopsis rei-like proteins activate ribosome biogenesis during cold acclimation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844247/
https://www.ncbi.nlm.nih.gov/pubmed/33510206
http://dx.doi.org/10.1038/s41598-021-81610-z
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