4.5 Article

Identification of a host 14-3-3 protein that interacts with Xanthomonas effector AvrRxv

期刊

PHYSIOLOGICAL AND MOLECULAR PLANT PATHOLOGY
卷 72, 期 1-3, 页码 46-55

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pmpp.2008.05.006

关键词

Avirulence protein; Yeast two-hybrid interaction screen; Effector; Hypersensitive response (HR); Xanthomonas campestris pv. vesicatoria; Yersinia enterocolitica; Solanum esculentum

资金

  1. NSF Cooperative Agreement [BIR-8920216]
  2. NIH [BIR-8920216, SO6GM52533, 5 R21 GM059022-01, 5 R25-GM64078, 5 R25-GM59298, 5 R25GM48972, 5T34-GM08574, RIMI P20 RR11805]
  3. NATIONAL CENTER FOR RESEARCH RESOURCES [P20RR011805] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R25GM064078, R25GM059298, S06GM052588, T34GM008574, R15GM059022, R25GM048972] Funding Source: NIH RePORTER

向作者/读者索取更多资源

AvrRxv is a member of a family of pathogen effectors present in pathogens of both plant and mammalian species. Xanthomonas campestris pv. vesicatoria strains carrying AvrRxv induce a hypersensitive response (HR) in the tomato cultivar Hawaii 7998. Using a yeast two-hybrid screen, we identified a 14-3-3 protein from tomato that interacts with AvrRxv called AvrRxv interactor 1 (ARI1). The interaction was confirmed in vitro with affinity chromatography. Using mutagenesis, we identified a 14-3-3-binding domain in AvrRxv and demonstrated that a mutant in that domain showed concomitant loss of interaction with ARI1 and HR-inducing activity in tomato. These results demonstrate that the AvrRxv bacterial effector recruits 14-3-3 proteins for its function within host cells. AvrRxv homologues YopP and YopJ from Yersinia do not have AvrRxv-specific HR-inducing activity when delivered into tomato host cells by Agrobacterium. Although YopP itself cannot induce HR, its C-terminal domain containing the catalytic residues can replace that of AvrRxv in an AvrRxv-YopP chimera for HR-inducing activity. Phylogenetic analysis indicates that the sequences encoding the C-termini of family members are evolving independently from those encoding the N-termini. Our results support a model in which there are three functional domains in proteins of the family: translocation, interaction, and catalytic. Published by Elsevier Ltd.

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