Poster
Rajalakshmi Reghunath
Leibniz Institute of Plant Biochemistry (IPB)
Halle(Saale),Saxony-Anhalt, Germany, GERMANY
Jörg Ziegler
Leibniz Institute of Plant Biochemistry (IPB)
Halle(Saale), Sachsen-Anhalt, Germany
Gerd Balcke
Leibniz Institute of Plant Biochemistry
Halle, Sachsen-Anhalt, Germany
Susanne Matschi
Postdoc
Leibniz-Institute of Plant Biochemistry
Halle, Sachsen-Anhalt, Germany
Domenika Thieme
Leibniz Institute of Plant Biochemistry
Halle Saale, Sachsen-Anhalt, Germany
Lennart Wirthmüller
Group Leader
Leibniz Institute of Plant Biochemistry (IPB)
Halle, Sachsen-Anhalt, Germany
Poly-ADP-ribosylation (PARylation) is a reversible post-translational protein modification. In PARylation, ‘writer’ enzymes of the Poly (ADP-ribose) polymerases (PARP) family repeatedly transfer ADP-ribose moieties from the co-substrate nicotinamide adenine dinucleotide (NAD+) onto target proteins, thereby catalysing the formation of long poly (ADP-ribose) chains. We report that an Arabidopsis thaliana parp1/2/3 higher-order mutant exhibits enhanced susceptibility to Botrytis cinerea. This elevated susceptibility towards a necrotrophic fungal pathogen correlates with higher transcript levels of salicylic acid-regulated defence genes in the mutant. Comparative metabolome profiling of the parp1/2/3 mutant and wild type plants in response to a PAMP stimulus suggest additional functions of PARPs in re-programming the phenylpropanoid branch of the defence metabolome. In order to place PARPs more precisely in the plant immunity network, we integrate proteomics data on PARP-interacting proteins and affinity enrichment of potential PARylated substrates. We will present on our current efforts to identify molecular links between PARPs and regulators of the defence transcriptome and metabolome.