Proteometabolomic analysis of transgenic tomato overexpressing oxalate decarboxylase uncovers novel proteins potentially involved in defense mechanism against Sclerotinia

Ghosh, Sudip ; Narula, Kanika ; Sinha, Arunima ; Ghosh, Rajgourab ; Jawa, Priyanka ; Chakraborty, Niranjan ; Chakraborty, Subhra (2016) Proteometabolomic analysis of transgenic tomato overexpressing oxalate decarboxylase uncovers novel proteins potentially involved in defense mechanism against Sclerotinia Journal of Proteomics, 143 . pp. 242-253. ISSN 18743919

Full text not available from this repository.

Official URL: http://doi.org/10.1016/j.jprot.2016.04.047

Related URL: http://dx.doi.org/10.1016/j.jprot.2016.04.047

Abstract

Oxalic acid (OA) plays dual role in fungal pathogenicity in a concentration dependent manner. While at higher concentration it induces programmed cell death leading to fungal invasion, low oxalate build resistance in plant. Although OA has been identified as a virulence determinant for rot disease caused by Sclerotinia sp., our understanding of how oxalate downregulation impart host immunity is limited. We have earlier shown that ectopic expression of oxalate decarboxylase (FvOXDC) specifically degrades OA in tomato (Solanum lycopersicum). To elucidate low oxalate regulated molecular mechanism imparting immunity, a comparative proteomics approach has been applied to E8.2-OXDC tomato fruit displaying fungal resistance. Mass spectrometric analyses identified 92 OXDC-responsive immunity related protein spots (ORIRPs) presumably associated with acid metabolism, defense signaling and endoplasmic reticulum stress. Metabolome study indicated increased abundance of some of the organic acids paralleling the proteomic analysis. Further, we interrogated the proteome data using network analysis that identified modules enriched in known and novel immunity-related prognostic proteins centered around 14-3-3, translationally controlled tumor protein, annexin and chaperonin. Taken together, our data demonstrate that low oxalate may act as metabolic and immunity determinant through translational reprogramming.

Item Type:Article
Source:Copyright of this article belongs to Elsevier B.V.
ID Code:132945
Deposited On:23 Dec 2022 08:43
Last Modified:23 Dec 2022 08:43

Repository Staff Only: item control page