Literature DB >> 16237208

Ancient origin of elicitin gene clusters in Phytophthora genomes.

Rays H Y Jiang1, Brett M Tyler, Stephen C Whisson, Adrienne R Hardham, Francine Govers.   

Abstract

The genus Phytophthora belongs to the oomycetes in the eukaryotic stramenopile lineage and is comprised of over 65 species that are all destructive plant pathogens on a wide range of dicotyledons. Phytophthora produces elicitins (ELIs), a group of extracellular elicitor proteins that cause a hypersensitive response in tobacco. Database mining revealed several new classes of elicitin-like (ELL) sequences with diverse elicitin domains in Phytophthora infestans, Phytophthora sojae, Phytophthora brassicae, and Phytophthora ramorum. ELIs and ELLs were shown to be unique to Phytophthora and Pythium species. They are ubiquitous among Phytophthora species and belong to one of the most highly conserved and complex protein families in the Phytophthora genus. Phylogeny construction with elicitin domains derived from 156 ELIs and ELLs showed that most of the diversified family members existed prior to divergence of Phytophthora species from a common ancestor. Analysis to discriminate diversifying and purifying selection showed that all 17 ELI and ELL clades are under purifying selection. Within highly similar ELI groups there was no evidence for positively selected amino acids suggesting that purifying selection contributes to the continued existence of this diverse protein family. Characteristic cysteine spacing patterns were found for each phylogenetic clade. Except for the canonical clade ELI-1, ELIs and ELLs possess C-terminal domains of variable length, many of which have a high threonine, serine, or proline content suggesting an association with the cell wall. In addition, some ELIs and ELLs have a predicted glycosylphosphatidylinositol site suggesting anchoring of the C-terminal domain to the cell membrane. The eli and ell genes belonging to different clades are clustered in the genomes. Overall, eli and ell genes are expressed at different levels and in different life cycle stages but those sharing the same phylogenetic clade appear to have similar expression patterns.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16237208     DOI: 10.1093/molbev/msj039

Source DB:  PubMed          Journal:  Mol Biol Evol        ISSN: 0737-4038            Impact factor:   16.240


  37 in total

1.  Amplification generates modular diversity at an avirulence locus in the pathogen Phytophthora.

Authors:  Rays H Y Jiang; Rob Weide; Peter J I van de Vondervoort; Francine Govers
Journal:  Genome Res       Date:  2006-07       Impact factor: 9.043

2.  Development of an Anti-Elicitin Antibody-Based Immunohistochemical Assay for Diagnosis of Pythiosis.

Authors:  Ruchuros Inkomlue; Noppadol Larbcharoensub; Patcharee Karnsombut; Tassanee Lerksuthirat; Rangsima Aroonroch; Tassanee Lohnoo; Wanta Yingyong; Pitak Santanirand; Lalana Sansopha; Theerapong Krajaejun
Journal:  J Clin Microbiol       Date:  2016-01       Impact factor: 5.948

3.  Evolution of the Sterol Biosynthetic Pathway of Pythium insidiosum and Related Oomycetes Contributes to Antifungal Drug Resistance.

Authors:  Tassanee Lerksuthirat; Areeporn Sangcakul; Tassanee Lohnoo; Wanta Yingyong; Thidarat Rujirawat; Theerapong Krajaejun
Journal:  Antimicrob Agents Chemother       Date:  2017-03-24       Impact factor: 5.191

4.  Cataloging proteins putatively secreted during the biotrophy-necrotrophy transition of the anthracnose pathogen Colletotrichum truncatum.

Authors:  Vijai Bhadauria; Sabine Banniza; Albert Vandenberg; Gopalan Selvaraj; Yangdou Wei
Journal:  Plant Signal Behav       Date:  2011-10-01

5.  Correlation of isozyme profiles with genomic sequences of Phytophthora ramorum and its P. sojae orthologues.

Authors:  Willem A Man In 't Veld; Francine Govers; Harold J G Meijer
Journal:  Curr Genet       Date:  2007-10-30       Impact factor: 3.886

6.  Transcriptome analysis of the entomopathogenic oomycete Lagenidium giganteum reveals putative virulence factors.

Authors:  Paula F Quiroz Velasquez; Sumayyah K Abiff; Katrina C Fins; Quincy B Conway; Norma C Salazar; Ana Paula Delgado; Jhanelle K Dawes; Lauren G Douma; Aurélien Tartar
Journal:  Appl Environ Microbiol       Date:  2014-08-08       Impact factor: 4.792

7.  Stigmasterol and cholesterol regulate the expression of elicitin genes in Phytophthora sojae.

Authors:  Lina F Yousef; Ahmed F Yousef; Joseph S Mymryk; Warren A Dick; Richard P Dick
Journal:  J Chem Ecol       Date:  2009-07-09       Impact factor: 2.626

8.  Distribution and expression of elicitin genes in the interspecific hybrid oomycete Phytophthora alni.

Authors:  Renaud Ioos; Franck Panabières; Benoît Industri; Axelle Andrieux; Pascal Frey
Journal:  Appl Environ Microbiol       Date:  2007-06-29       Impact factor: 4.792

Review 9.  Expanding the paradigms of plant pathogen life history and evolution of parasitic fitness beyond agricultural boundaries.

Authors:  Cindy E Morris; Marc Bardin; Linda L Kinkel; Benoit Moury; Philippe C Nicot; David C Sands
Journal:  PLoS Pathog       Date:  2009-12-24       Impact factor: 6.823

10.  Isolation and characterization of NgRLK1, a receptor-like kinase of Nicotiana glutinosa that interacts with the elicitin of Phytophthora capsici.

Authors:  Yeong-Tae Kim; Jonghee Oh; Kyung-Hwan Kim; Jae-Youl Uhm; Byoung-Moo Lee
Journal:  Mol Biol Rep       Date:  2009-05-16       Impact factor: 2.316

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.