Abstract

BackgroundThe Arabidopsis thaliana NPR1 gene encodes a transcription coactivator (NPR1) that plays a major role in the mechanisms regulating plant defense response. After pathogen infection and in response to salicylic acid (SA) accumulation, NPR1 translocates from the cytoplasm into the nucleus where it interacts with other transcription factors resulting in increased expression of over 2000 plant defense genes contributing to a pathogen resistance response.ResultsA putative Theobroma cacao NPR1 cDNA was isolated by RT-PCR using degenerate primers based on homologous sequences from Brassica, Arabidopsis and Carica papaya. The cDNA was used to isolate a genomic clone from Theobroma cacao containing a putative TcNPR1 gene. DNA sequencing revealed the presence of a 4.5 kb coding region containing three introns and encoding a polypeptide of 591 amino acids. The predicted TcNPR1 protein shares 55% identity and 78% similarity to Arabidopsis NPR1, and contains each of the highly conserved functional domains indicative of this class of transcription factors (BTB/POZ and ankyrin repeat protein-protein interaction domains and a nuclear localization sequence (NLS)). To functionally define the TcNPR1 gene, we transferred TcNPR1 into an Arabidopsis npr1 mutant that is highly susceptible to infection by the plant pathogen Pseudomonas syringae pv. tomato DC3000. Driven by the constitutive CaMV35S promoter, the cacao TcNPR1 gene partially complemented the npr1 mutation in transgenic Arabidopsis plants, resulting in 100 fold less bacterial growth in a leaf infection assay. Upon induction with SA, TcNPR1 was shown to translocate into the nucleus of leaf and root cells in a manner identical to Arabidopsis NPR1. Cacao NPR1 was also capable of participating in SA-JA signaling crosstalk, as evidenced by the suppression of JA responsive gene expression in TcNPR1 overexpressing transgenic plants.ConclusionOur data indicate that the TcNPR1 is a functional ortholog of Arabidopsis NPR1, and is likely to play a major role in defense response in cacao. This fundamental knowledge can contribute to breeding of disease resistant cacao varieties through the application of molecular markers or the use of transgenic strategies.

Highlights

  • The Arabidopsis thaliana Non-Expressor of PR1 (NPR1) gene encodes a transcription coactivator (NPR1) that plays a major role in the mechanisms regulating plant defense response

  • The degenerate primers were designed based on the alignment of NPR1 homologs from Arabidopsis, Brassica and Carica papaya and cDNA from cacao genotype Scavina6 (SCA6) leaf was used as template

  • A genomic fragment containing a putative Theobroma cacao NPR1 (TcNPR1) gene was obtained by screening Clemson University Genomics Institute (CUGI) cacao BAC library using the putative cacao TcNPR1 cDNA clone as probe

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Summary

Introduction

The Arabidopsis thaliana NPR1 gene encodes a transcription coactivator (NPR1) that plays a major role in the mechanisms regulating plant defense response. After pathogen infection and in response to salicylic acid (SA) accumulation, NPR1 translocates from the cytoplasm into the nucleus where it interacts with other transcription factors resulting in increased expression of over 2000 plant defense genes contributing to a pathogen resistance response. Induction of the SAR pathway leads to heightened broad-spectrum resistance to secondary pathogen attacks by a variety of pathogens. Multiple studies in both monocots and dicots have shown that salicylic acid (SA) plays a central role as a signaling molecule in SAR [7,8,9,10,11,12,13,14]. SA is required for the induced expression of a set of pathogenesis-related (PR) genes [7,15,16,17]

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