Snf1-RELATED KINASE1-Controlled C/S(1)-bZIP Signaling Activates Alternative Mitochondrial Metabolic Pathways to Ensure Plant Survival in Extended Darkness
L. Pedrotti, C. Weiste, T. Nagele, E. Wolf, F. Lorenzin, K. Dietrich, A. Mair, W. Weckwerth, M. Teige, E. Baena-Gonzalez, and W. Droge-Laser. Plant Cell, 30 (2):
495-509(2018)Pedrotti, Lorenzo
Weiste, Christoph
Nagele, Thomas
Wolf, Elmar
Lorenzin, Francesca
Dietrich, Katrin
Mair, Andrea
Weckwerth, Wolfram
Teige, Markus
Baena-Gonzalez, Elena
Droge-Laser, Wolfgang
eng
P 28491/FWF_/Austrian Science Fund FWF/Austria
Research Support, Non-U.S. Gov't
England
2018/01/20
Plant Cell. 2018 Feb;30(2):495-509. doi: 10.1105/tpc.17.00414. Epub 2018 Jan 18..
DOI: 10.1105/tpc.17.00414
Abstract
Sustaining energy homeostasis is of pivotal importance for all living organisms. In Arabidopsis thaliana, evolutionarily conserved SnRK1 kinases (Snf1-RELATED KINASE1) control metabolic adaptation during low energy stress. To unravel starvation-induced transcriptional mechanisms, we performed transcriptome studies of inducible knockdown lines and found that S(1)-basic leucine zipper transcription factors (S(1)-bZIPs) control a defined subset of genes downstream of SnRK1. For example, S(1)-bZIPs coordinate the expression of genes involved in branched-chain amino acid catabolism, which constitutes an alternative mitochondrial respiratory pathway that is crucial for plant survival during starvation. Molecular analyses defined S(1)-bZIPs as SnRK1-dependent regulators that directly control transcription via binding to G-box promoter elements. Moreover, SnRK1 triggers phosphorylation of group C-bZIPs and the formation of C/S(1)-heterodimers and, thus, the recruitment of SnRK1 directly to target promoters. Subsequently, the C/S(1)-bZIP-SnRK1 complex interacts with the histone acetylation machinery to remodel chromatin and facilitate transcription. Taken together, this work reveals molecular mechanisms underlying how energy deprivation is transduced to reprogram gene expression, leading to metabolic adaptation upon stress.
Pedrotti, Lorenzo
Weiste, Christoph
Nagele, Thomas
Wolf, Elmar
Lorenzin, Francesca
Dietrich, Katrin
Mair, Andrea
Weckwerth, Wolfram
Teige, Markus
Baena-Gonzalez, Elena
Droge-Laser, Wolfgang
eng
P 28491/FWF_/Austrian Science Fund FWF/Austria
Research Support, Non-U.S. Gov't
England
2018/01/20
Plant Cell. 2018 Feb;30(2):495-509. doi: 10.1105/tpc.17.00414. Epub 2018 Jan 18.
%0 Journal Article
%1 pedrotti2018snf1related
%A Pedrotti, L.
%A Weiste, C.
%A Nagele, T.
%A Wolf, E.
%A Lorenzin, F.
%A Dietrich, K.
%A Mair, A.
%A Weckwerth, W.
%A Teige, M.
%A Baena-Gonzalez, E.
%A Droge-Laser, W.
%D 2018
%J Plant Cell
%K Adaptation, Physiological myOwn uni_network
%N 2
%P 495-509
%R 10.1105/tpc.17.00414
%T Snf1-RELATED KINASE1-Controlled C/S(1)-bZIP Signaling Activates Alternative Mitochondrial Metabolic Pathways to Ensure Plant Survival in Extended Darkness
%U https://www.ncbi.nlm.nih.gov/pubmed/29348240https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868691/pdf/PC_TPC2017RA00414R1.pdf
%V 30
%X Sustaining energy homeostasis is of pivotal importance for all living organisms. In Arabidopsis thaliana, evolutionarily conserved SnRK1 kinases (Snf1-RELATED KINASE1) control metabolic adaptation during low energy stress. To unravel starvation-induced transcriptional mechanisms, we performed transcriptome studies of inducible knockdown lines and found that S(1)-basic leucine zipper transcription factors (S(1)-bZIPs) control a defined subset of genes downstream of SnRK1. For example, S(1)-bZIPs coordinate the expression of genes involved in branched-chain amino acid catabolism, which constitutes an alternative mitochondrial respiratory pathway that is crucial for plant survival during starvation. Molecular analyses defined S(1)-bZIPs as SnRK1-dependent regulators that directly control transcription via binding to G-box promoter elements. Moreover, SnRK1 triggers phosphorylation of group C-bZIPs and the formation of C/S(1)-heterodimers and, thus, the recruitment of SnRK1 directly to target promoters. Subsequently, the C/S(1)-bZIP-SnRK1 complex interacts with the histone acetylation machinery to remodel chromatin and facilitate transcription. Taken together, this work reveals molecular mechanisms underlying how energy deprivation is transduced to reprogram gene expression, leading to metabolic adaptation upon stress.
@article{pedrotti2018snf1related,
abstract = {Sustaining energy homeostasis is of pivotal importance for all living organisms. In Arabidopsis thaliana, evolutionarily conserved SnRK1 kinases (Snf1-RELATED KINASE1) control metabolic adaptation during low energy stress. To unravel starvation-induced transcriptional mechanisms, we performed transcriptome studies of inducible knockdown lines and found that S(1)-basic leucine zipper transcription factors (S(1)-bZIPs) control a defined subset of genes downstream of SnRK1. For example, S(1)-bZIPs coordinate the expression of genes involved in branched-chain amino acid catabolism, which constitutes an alternative mitochondrial respiratory pathway that is crucial for plant survival during starvation. Molecular analyses defined S(1)-bZIPs as SnRK1-dependent regulators that directly control transcription via binding to G-box promoter elements. Moreover, SnRK1 triggers phosphorylation of group C-bZIPs and the formation of C/S(1)-heterodimers and, thus, the recruitment of SnRK1 directly to target promoters. Subsequently, the C/S(1)-bZIP-SnRK1 complex interacts with the histone acetylation machinery to remodel chromatin and facilitate transcription. Taken together, this work reveals molecular mechanisms underlying how energy deprivation is transduced to reprogram gene expression, leading to metabolic adaptation upon stress.},
added-at = {2024-02-15T15:08:22.000+0100},
author = {Pedrotti, L. and Weiste, C. and Nagele, T. and Wolf, E. and Lorenzin, F. and Dietrich, K. and Mair, A. and Weckwerth, W. and Teige, M. and Baena-Gonzalez, E. and Droge-Laser, W.},
biburl = {https://www.bibsonomy.org/bibtex/2517f79d92577c174a82df0ae282a11a9/jvsi_all},
doi = {10.1105/tpc.17.00414},
interhash = {aa344c4626bd5ededd1e44954e202efc},
intrahash = {517f79d92577c174a82df0ae282a11a9},
issn = {1532-298X (Electronic)
1040-4651 (Print)
1040-4651 (Linking)},
journal = {Plant Cell},
keywords = {Adaptation, Physiological myOwn uni_network},
note = {Pedrotti, Lorenzo
Weiste, Christoph
Nagele, Thomas
Wolf, Elmar
Lorenzin, Francesca
Dietrich, Katrin
Mair, Andrea
Weckwerth, Wolfram
Teige, Markus
Baena-Gonzalez, Elena
Droge-Laser, Wolfgang
eng
P 28491/FWF_/Austrian Science Fund FWF/Austria
Research Support, Non-U.S. Gov't
England
2018/01/20
Plant Cell. 2018 Feb;30(2):495-509. doi: 10.1105/tpc.17.00414. Epub 2018 Jan 18.},
number = 2,
pages = {495-509},
timestamp = {2024-02-15T15:11:55.000+0100},
title = {Snf1-RELATED KINASE1-Controlled C/S(1)-bZIP Signaling Activates Alternative Mitochondrial Metabolic Pathways to Ensure Plant Survival in Extended Darkness},
type = {Journal Article},
url = {https://www.ncbi.nlm.nih.gov/pubmed/29348240https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868691/pdf/PC_TPC2017RA00414R1.pdf},
volume = 30,
year = 2018
}