Loading…

Characterization of a pathogenesis-related protein 4 (PR-4) induced in Capsicum chinense L super(3) plants with dual RNase and DNase activities

Resistance conferred by the L super(3) gene is active against most of the tobamoviruses, including the Spanish strain (PMMoV-S), a P sub(1), sub(2) pathotype, but not against certain strains of pepper mild mottle virus (PMMoV), termed as P sub(1), sub(2), sub(3) pathotype, such as the Italian strain...

Full description

Saved in:
Bibliographic Details
Published in:Journal of experimental botany 2010-01, Vol.61 (12), p.3259-3271
Main Authors: Guevara-Morato, Maria Angeles, de Lacoba, Mario Garcia, Garcia-Luque, Isabel, Serra, Maria Teresa
Format: Article
Language:English
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Resistance conferred by the L super(3) gene is active against most of the tobamoviruses, including the Spanish strain (PMMoV-S), a P sub(1), sub(2) pathotype, but not against certain strains of pepper mild mottle virus (PMMoV), termed as P sub(1), sub(2), sub(3) pathotype, such as the Italian strain (PMMoV-I). PMMoV-S induces a hypersensitive reaction (HR) in C. chinense PI159236 plant leaves with the formation of necrotic local lesions and restriction of the virus at the primary infection sites. In this paper, a C. chinense PR-4 protein induced during both the compatible and the incompatible interactions has been identified. It was strongly associated with HR induction and to a lesser extent with the compatible interaction, but only in the later stages of infection. Moreover, it was found to accumulate during the necrogenic reaction induced by Potato virus X. The C. chinense PR-4 protein belongs to the PR-4 protein subgroup II, based on the absence of a hevein domain. Furthermore, it is shown that the purified protein does not have chitinase activity, as previously proposed for PR-4 proteins. Instead, it has both RNase and DNase activity, although its contribution to the bulk activity of nucleases in infected plants is very low.
ISSN:0022-0957
1460-2431
DOI:10.1093/jxb/erq148