Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.601038
Title: Structure-function studies of translocated effectors from the late blight pathogen
Author: King, Stuart
Awarding Body: University of East Anglia
Current Institution: University of East Anglia
Date of Award: 2013
Availability of Full Text:
Access from EThOS:
Access from Institution:
Abstract:
An almost universal feature of successful pathogens is the secretion of effector proteins, many of which translocate inside host cells. These effectors manipulate host processes for the pathogen’s benefit. However, in response to this manipulation, plants have evolved to monitor for effectors and trigger defence responses. Amongst plant pathogens, oomycetes of the genus Phytophthora have arguably caused almost unrivalled levels of human suffering and represent significant threats to global food security. The late blight pathogen, Phytophthora infestans, is the most devastating pathogen of potato – the fourth most important food crop worldwide. Effective and durable resistance against late blight is desperately needed; and will depend on an improved understanding of the mechanistic basis of disease. Determining the adaptive functions of effectors might reveal previously unexploited management strategies. This work details structure-function studies of two translocated effectors from the late blight pathogen; PexRD2, a representative RXLR effector, and CRN8, an effector with kinase activity. Efforts to heterologously express CRN8 were hampered by protein insolubility and low yields. However, the crystal structure of PexRD2 revealed that it homodimerises, and was crucial to the discovery of a conserved oomycete effector protein fold, the WY-domain fold. Yeast two-hybrid screening identified four PexRD2-interacting host proteins, including MAPKKKε, a known positive regulator of plant immunity. MAP-kinase cascades transduce the perception of invading pathogens into effective defence responses, and MAPKKKε is involved in resistance against P. infestans. PexRD2 specifically suppresses cell deaths that are either MAPKKKε-dependent or triggered by MAPKKKε overexpression. PexRD2 also inhibits MAPKKKε-triggered MAPK activation. Further, structure-led mutagenesis of PexRD2 suggests that this effector benefits the pathogen by interacting with MAPKKKε to inhibit the kinase’s signalling. Discovering the PexRD2-MAPKKKε interaction, and its implications for plant immunity, has suggested unexploited management strategies that could enhance crop resistance to this devastating pathogen.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.601038  DOI: Not available
Share: