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Snf1-RELATED KINASE1-Controlled C/S1-bZIP Signaling Activates Alternative Mitochondrial Metabolic Pathways to Ensure Plant Survival in Extended Darkness
Author(s) -
Lorenzo Pedrotti,
Christoph Weiste,
Thomas Nägele,
Elmar Wolf,
Francesca Lorenzin,
Katrin Dietrich,
Andrea Mair,
Wolfram Weckwerth,
Markus Teige,
Elena Baena–González,
Wolfgang DrögeLaser
Publication year - 2018
Publication title -
the plant cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.324
H-Index - 341
eISSN - 1532-298X
pISSN - 1040-4651
DOI - 10.1105/tpc.17.00414
Subject(s) - biology , transcription factor , microbiology and biotechnology , gene knockdown , histone , chromatin , gene , transcription (linguistics) , transcriptional regulation , regulation of gene expression , chromatin remodeling , arabidopsis , psychological repression , promoter , genetics , gene expression , mutant , linguistics , philosophy
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.

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