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Publikation

Wang, J.-Z.; Li, B.; Xiao, Y.; Ni, Y.; Ke, H.; Yang, P.; de Souza, A.; Bjornson, M.; He, X.; Shen, Z.; Balcke, G. U.; Briggs, S. P.; Tissier, A.; Kliebenstein, D. J.; Dehesh, K.; Initiation of ER Body Formation and Indole Glucosinolate Metabolism by the Plastidial Retrograde Signaling Metabolite, MEcPP Mol. Plant 10, 1400-1416, (2017) DOI: 10.1016/j.molp.2017.09.012

Plants have evolved tightly regulated signaling networks to respond and adapt to environmental perturbations, but the nature of the signaling hub(s) involved have remained an enigma. We have previously established that methylerythritol cyclodiphosphate (MEcPP), a precursor of plastidial isoprenoids and a stress-specific retrograde signaling metabolite, enables cellular readjustments for high-order adaptive functions. Here, we specifically show that MEcPP promotes two Brassicaceae-specific traits, namely endoplasmic reticulum (ER) body formation and induction of indole glucosinolate (IGs) metabolism selectively, via transcriptional regulation of key regulators NAI1 for ER body formation and MYB51/122 for IGs biosynthesis). The specificity of MEcPP is further confirmed by the lack of induction of wound-inducible ER body genes as well as IGs by other altered methylerythritol phosphate pathway enzymes. Genetic analyses revealed MEcPP-mediated COI1-dependent induction of these traits. Moreover, MEcPP signaling integrates the biosynthesis and hydrolysis of IGs through induction of nitrile-specifier protein1 and reduction of the suppressor, ESM1, and production of simple nitriles as the bioactive end product. The findings position the plastidial metabolite, MEcPP, as the initiation hub, transducing signals to adjust the activity of hard-wired gene circuitry to expand phytochemical diversity and alter the associated subcellular structure required for functionality of the secondary metabolites, thereby tailoring plant stress responses.
Publikation

Bjornson, M.; Balcke, G. U.; Xiao, Y.; de Souza, A.; Wang, J.-Z.; Zhabinskaya, D.; Tagkopoulos, I.; Tissier, A.; Dehesh, K.; Integrated omics analyses of retrograde signaling mutant delineate interrelated stress-response strata Plant J. 91, 70-84, (2017) DOI: 10.1111/tpj.13547

To maintain homeostasis in the face of intrinsic and extrinsic insults, cells have evolved elaborate quality control networks to resolve damage at multiple levels. Interorganellar communication is a key requirement for this maintenance, however the underlying mechanisms of this communication have remained an enigma. Here we integrate the outcome of transcriptomic, proteomic, and metabolomics analyses of genotypes including ceh1, a mutant with constitutively elevated levels of both the stress‐specific plastidial retrograde signaling metabolite methyl‐erythritol cyclodiphosphate (MEcPP) and the defense hormone salicylic acid (SA), as well as the high MEcPP but SA deficient genotype ceh1/eds16, along with corresponding controls. Integration of multi‐omic analyses enabled us to delineate the function of MEcPP from SA, and expose the compartmentalized role of this retrograde signaling metabolite in induction of distinct but interdependent signaling cascades instrumental in adaptive responses. Specifically, here we identify strata of MEcPP‐sensitive stress‐response cascades, among which we focus on selected pathways including organelle‐specific regulation of jasmonate biosynthesis; simultaneous induction of synthesis and breakdown of SA; and MEcPP‐mediated alteration of cellular redox status in particular glutathione redox balance. Collectively, these integrated multi‐omic analyses provided a vehicle to gain an in‐depth knowledge of genome‐metabolism interactions, and to further probe the extent of these interactions and delineate their functional contributions. Through this approach we were able to pinpoint stress‐mediated transcriptional and metabolic signatures and identify the downstream processes modulated by the independent or overlapping functions of MEcPP and SA in adaptive responses.
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