Plant Cell Bio-Rad Microplate Reader
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


First published online August 3, 2007; 10.1105/tpc.107.051037

The Plant Cell 19:2349-2369 (2007)
© 2007 American Society of Plant Biologists

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplemental Data
Right arrow All Versions of this Article:
19/8/2349    most recent
tpc.107.051037v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Related articles in Plant Cell
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (5)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Win, J.
Right arrow Articles by Kamoun, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Win, J.
Right arrow Articles by Kamoun, S.
Agricola
Right arrow Articles by Win, J.
Right arrow Articles by Kamoun, S.

Adaptive Evolution Has Targeted the C-Terminal Domain of the RXLR Effectors of Plant Pathogenic Oomycetes[W]

Joe Wina, William Morganb, Jorunn Bosa, Ksenia V. Krasilevac, Liliana M. Canoa, Angela Chaparro-Garciaa, Randa Ammara, Brian J. Staskawiczc and Sophien Kamouna,1

a Department of Plant Pathology, Ohio State University Ohio Agricultural Research and Development Center, Wooster, Ohio 44691
b Department of Biology, College of Wooster, Wooster, Ohio 44691
c Department of Plant and Microbial Biology, University of California, Berkeley, California 94270

1 Address correspondence to kamoun.1{at}osu.edu.

Oomycete plant pathogens deliver effector proteins inside host cells to modulate plant defense circuitry and to enable parasitic colonization. These effectors are defined by a conserved motif, termed RXLR (for Arg, any amino acid, Leu, Arg), that is located downstream of the signal peptide and that has been implicated in host translocation. Because the phenotypes of RXLR effectors extend to plant cells, their genes are expected to be the direct target of the evolutionary forces that drive the antagonistic interplay between pathogen and host. We used the draft genome sequences of three oomycete plant pathogens, Phytophthora sojae, Phytophthora ramorum, and Hyaloperonospora parasitica, to generate genome-wide catalogs of RXLR effector genes and determine the extent to which these genes are under positive selection. These analyses revealed that the RXLR sequence is overrepresented and positionally constrained in the secretome of Phytophthora relative to other eukaryotes. The three examined plant pathogenic oomycetes carry complex and diverse sets of RXLR effector genes that have undergone relatively rapid birth and death evolution. We obtained robust evidence of positive selection in more than two-thirds of the examined paralog families of RXLR effectors. Positive selection has acted for the most part on the C-terminal region, consistent with the view that RXLR effectors are modular, with the N terminus involved in secretion and host translocation and the C-terminal domain dedicated to modulating host defenses inside plant cells.


Related articles in Plant Cell:

Adaptive Evolution among Plant Pathogenic Oomycte RXLR Effector Genes
Nancy A. Eckardt
Plant Cell 2007 19: 2322. [Full Text]  



This article has been cited by other articles:


Home page
Mol PlantHome page
J. Liu and G. Coaker
Nuclear Trafficking During Plant Innate Immunity
Mol Plant, April 1, 2008; (2008) ssn010v1.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
R. H. Y. Jiang, S. Tripathy, F. Govers, and B. M. Tyler
RXLR effector reservoir in two Phytophthora species is dominated by a single rapidly evolving superfamily with more than 700 members
PNAS, March 25, 2008; 105(12): 4874 - 4879.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
M. C. Rentel, L. Leonelli, D. Dahlbeck, B. Zhao, and B. J. Staskawicz
Recognition of the Hyaloperonospora parasitica effector ATR13 triggers resistance against oomycete, bacterial, and viral pathogens
PNAS, January 22, 2008; 105(3): 1091 - 1096.
[Abstract] [Full Text] [PDF]


Home page
Plant CellHome page
K. H. Sohn, R. Lei, A. Nemri, and J. D.G. Jones
The Downy Mildew Effector Proteins ATR1 and ATR13 Promote Disease Susceptibility in Arabidopsis thaliana
PLANT CELL, December 1, 2007; 19(12): 4077 - 4090.
[Abstract] [Full Text] [PDF]


Home page
Plant CellHome page
D. M. Soanes, T. A. Richards, and N. J. Talbot
Insights from Sequencing Fungal and Oomycete Genomes: What Can We Learn about Plant Disease and the Evolution of Pathogenicity?
PLANT CELL, November 1, 2007; 19(11): 3318 - 3326.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications THE PLANT CELL PLANT PHYSIOLOGY
Copyright © 2007 by the American Society of Plant Biologists