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SNF1-Related Protein Kinase 1 Activity Represses the Canonical Translational Machinery

Protein biosynthesis is achieved through translation, which consumes enormous energy. Therefore, under conditions of limited energy supply, translation progress should be strictly coordinated. Sucrose non-fermenting kinase1 (SNF1)-related protein kinase 1 (SnRK1) is an evolutionarily conserved maste...

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Autores principales: Son, Seungmin, Im, Jong Hee, Song, Giha, Park, Sang Ryeol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9147276/
https://www.ncbi.nlm.nih.gov/pubmed/35631784
http://dx.doi.org/10.3390/plants11101359
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author Son, Seungmin
Im, Jong Hee
Song, Giha
Park, Sang Ryeol
author_facet Son, Seungmin
Im, Jong Hee
Song, Giha
Park, Sang Ryeol
author_sort Son, Seungmin
collection PubMed
description Protein biosynthesis is achieved through translation, which consumes enormous energy. Therefore, under conditions of limited energy supply, translation progress should be strictly coordinated. Sucrose non-fermenting kinase1 (SNF1)-related protein kinase 1 (SnRK1) is an evolutionarily conserved master regulator of cellular energy stress signaling in plants. Rice (Oryza sativa) and Arabidopsis (Arabidopsis thaliana) SnRK1 enhance hypoxia tolerance and induce the expression of stress-related genes. However, whether SnRK1 modulates protein synthesis in plants is unknown. In this study, using translational reporter constructs transfected in Arabidopsis protoplasts we showed that the expression of OsSnRK1A and AtSnRK1.1 decreases the abundance of canonical proteins without affecting their encoding transcript levels and protein stability. Moreover, the loading of total mRNAs and GFP mRNAs into the heavy polysome fraction which is normally translated was attenuated in transgenic Arabidopsis lines constitutively expressing OsSnRK1A or AtSnRK1.1. Taken together, these results suggest that OsSnRK1A and AtSnRK1.1 suppress protein translation to maintain energy homeostasis.
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spelling pubmed-91472762022-05-29 SNF1-Related Protein Kinase 1 Activity Represses the Canonical Translational Machinery Son, Seungmin Im, Jong Hee Song, Giha Park, Sang Ryeol Plants (Basel) Communication Protein biosynthesis is achieved through translation, which consumes enormous energy. Therefore, under conditions of limited energy supply, translation progress should be strictly coordinated. Sucrose non-fermenting kinase1 (SNF1)-related protein kinase 1 (SnRK1) is an evolutionarily conserved master regulator of cellular energy stress signaling in plants. Rice (Oryza sativa) and Arabidopsis (Arabidopsis thaliana) SnRK1 enhance hypoxia tolerance and induce the expression of stress-related genes. However, whether SnRK1 modulates protein synthesis in plants is unknown. In this study, using translational reporter constructs transfected in Arabidopsis protoplasts we showed that the expression of OsSnRK1A and AtSnRK1.1 decreases the abundance of canonical proteins without affecting their encoding transcript levels and protein stability. Moreover, the loading of total mRNAs and GFP mRNAs into the heavy polysome fraction which is normally translated was attenuated in transgenic Arabidopsis lines constitutively expressing OsSnRK1A or AtSnRK1.1. Taken together, these results suggest that OsSnRK1A and AtSnRK1.1 suppress protein translation to maintain energy homeostasis. MDPI 2022-05-20 /pmc/articles/PMC9147276/ /pubmed/35631784 http://dx.doi.org/10.3390/plants11101359 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Son, Seungmin
Im, Jong Hee
Song, Giha
Park, Sang Ryeol
SNF1-Related Protein Kinase 1 Activity Represses the Canonical Translational Machinery
title SNF1-Related Protein Kinase 1 Activity Represses the Canonical Translational Machinery
title_full SNF1-Related Protein Kinase 1 Activity Represses the Canonical Translational Machinery
title_fullStr SNF1-Related Protein Kinase 1 Activity Represses the Canonical Translational Machinery
title_full_unstemmed SNF1-Related Protein Kinase 1 Activity Represses the Canonical Translational Machinery
title_short SNF1-Related Protein Kinase 1 Activity Represses the Canonical Translational Machinery
title_sort snf1-related protein kinase 1 activity represses the canonical translational machinery
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9147276/
https://www.ncbi.nlm.nih.gov/pubmed/35631784
http://dx.doi.org/10.3390/plants11101359
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