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Snf1 相关激酶 1 调控的 C/S-bZIP 信号激活替代的线粒体代谢途径以确保植物在延长的黑暗中存活。

Snf1-RELATED KINASE1-Controlled C/S-bZIP Signaling Activates Alternative Mitochondrial Metabolic Pathways to Ensure Plant Survival in Extended Darkness.

机构信息

Department of Pharmaceutical Biology, Julius-von-Sachs-Institute, Biocenter, Julius-Maximilians-Universität Würzburg, Würzburg 97082, Germany.

Department of Ecogenomics and Systems Biology, University of Vienna, Vienna 1090, Austria.

出版信息

Plant Cell. 2018 Feb;30(2):495-509. doi: 10.1105/tpc.17.00414. Epub 2018 Jan 18.

Abstract

Sustaining energy homeostasis is of pivotal importance for all living organisms. In , 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-basic leucine zipper transcription factors (S-bZIPs) control a defined subset of genes downstream of SnRK1. For example, S-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-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-heterodimers and, thus, the recruitment of SnRK1 directly to target promoters. Subsequently, the C/S-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.

摘要

维持能量平衡对所有生物体都至关重要。在进化上保守的 SnRK1 激酶(Snf1-RELATED KINASE1)在能量应激时控制代谢适应。为了揭示饥饿诱导的转录机制,我们对诱导型敲低系进行了转录组研究,发现 S-碱性亮氨酸拉链转录因子(S-bZIPs)在 SnRK1 下游控制着一组特定的基因。例如,S-bZIPs 协调涉及支链氨基酸分解代谢的基因的表达,这构成了替代的线粒体呼吸途径,对植物在饥饿期间的生存至关重要。分子分析将 S-bZIPs 定义为 SnRK1 依赖性调节剂,通过结合 G 框启动子元件直接控制转录。此外,SnRK1 触发 C 组 bZIP 的磷酸化和 C/S-异二聚体的形成,从而将 SnRK1 直接募集到靶启动子上。随后,C/S-bZIP-SnRK1 复合物与组蛋白乙酰化机制相互作用,重塑染色质并促进转录。总之,这项工作揭示了能量剥夺如何转导到重编程基因表达,从而导致应激时代谢适应的分子机制。

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