Literature DB >> 12073092

Distribution of the pea pathogenicity ( PEP) genes in the fungus Nectria haematococca mating population VI.

Esteban D Temporini1, Hans D VanEtten.   

Abstract

Previous studies identified a cluster of six genes that are expressed in the fungus Nectria haematococca mating population VI during infection of pea. Four of these genes were shown to contribute to pathogenicity on pea and were called PEP genes for pea pathogenicity. The cluster is located on a "conditionally dispensable" (CD) chromosome and has features similar to bacterial pathogenicity islands. In this study, the occurrence and location of members of the PEP cluster were analyzed in laboratory strains and nine pea pathogenic and 16 non-pea pathogenic field isolates of N. haematococca. Our results indicate that all pea-pathogenic isolates have homologues for all six genes present in the PEP cluster and the homologues appear to be clustered. PEP homologues are also present in isolates that are not pathogenic on pea, although none of these isolates have homologues of all six genes. In addition, PEP homologues are found in CD chromosomes and in other chromosomes. Isolates without PEP homologues are virulent on ripe tomato fruits and carrot roots, indicating that PEP genes are not required for pathogenicity on these hosts.

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Year:  2002        PMID: 12073092     DOI: 10.1007/s00294-002-0279-x

Source DB:  PubMed          Journal:  Curr Genet        ISSN: 0172-8083            Impact factor:   3.886


  8 in total

1.  The supernumerary chromosome of Nectria haematococca that carries pea-pathogenicity-related genes also carries a trait for pea rhizosphere competitiveness.

Authors:  M Rodriguez-Carres; G White; D Tsuchiya; M Taga; H D VanEtten
Journal:  Appl Environ Microbiol       Date:  2008-04-11       Impact factor: 4.792

Review 2.  Evolution and genome architecture in fungal plant pathogens.

Authors:  Mareike Möller; Eva H Stukenbrock
Journal:  Nat Rev Microbiol       Date:  2017-08-07       Impact factor: 60.633

3.  Comparative genomic and transcriptomic analyses of trans-kingdom pathogen Fusarium solani species complex reveal degrees of compartmentalization.

Authors:  Daphne Z Hoh; Hsin-Han Lee; Naohisa Wada; Wei-An Liu; Min R Lu; Cheng-Kuo Lai; Huei-Mien Ke; Pei-Feng Sun; Sen-Lin Tang; Wen-Hsin Chung; Ying-Lien Chen; Chia-Lin Chung; Isheng Jason Tsai
Journal:  BMC Biol       Date:  2022-10-20       Impact factor: 7.364

4.  An analysis of the phylogenetic distribution of the pea pathogenicity genes of Nectria haematococca MPVI supports the hypothesis of their origin by horizontal transfer and uncovers a potentially new pathogen of garden pea: Neocosmospora boniensis.

Authors:  Esteban D Temporini; Hans D VanEtten
Journal:  Curr Genet       Date:  2004-04-30       Impact factor: 3.886

5.  Expression profiles of pea pathogenicity ( PEP) genes in vivo and in vitro, characterization of the flanking regions of the PEP cluster and evidence that the PEP cluster region resulted from horizontal gene transfer in the fungal pathogen Nectria haematococca.

Authors:  Xiaoguang Liu; Mark Inlow; Hans D VanEtten
Journal:  Curr Genet       Date:  2003-08-19       Impact factor: 3.886

6.  Enemy or ally: a genomic approach to elucidate the lifestyle of Phyllosticta citrichinaensis.

Authors:  Valerie A Buijs; Johannes Z Groenewald; Sajeet Haridas; Kurt M LaButti; Anna Lipzen; Francis M Martin; Kerrie Barry; Igor V Grigoriev; Pedro W Crous; Michael F Seidl
Journal:  G3 (Bethesda)       Date:  2022-05-06       Impact factor: 3.542

7.  A chromosome-scale genome assembly of the tomato pathogen Cladosporium fulvum reveals a compartmentalized genome architecture and the presence of a dispensable chromosome.

Authors:  Alex Z Zaccaron; Li-Hung Chen; Anastasios Samaras; Ioannis Stergiopoulos
Journal:  Microb Genom       Date:  2022-04

8.  The genome of Nectria haematococca: contribution of supernumerary chromosomes to gene expansion.

Authors:  Jeffrey J Coleman; Steve D Rounsley; Marianela Rodriguez-Carres; Alan Kuo; Catherine C Wasmann; Jane Grimwood; Jeremy Schmutz; Masatoki Taga; Gerard J White; Shiguo Zhou; David C Schwartz; Michael Freitag; Li-Jun Ma; Etienne G J Danchin; Bernard Henrissat; Pedro M Coutinho; David R Nelson; Dave Straney; Carolyn A Napoli; Bridget M Barker; Michael Gribskov; Martijn Rep; Scott Kroken; István Molnár; Christopher Rensing; John C Kennell; Jorge Zamora; Mark L Farman; Eric U Selker; Asaf Salamov; Harris Shapiro; Jasmyn Pangilinan; Erika Lindquist; Casey Lamers; Igor V Grigoriev; David M Geiser; Sarah F Covert; Esteban Temporini; Hans D Vanetten
Journal:  PLoS Genet       Date:  2009-08-28       Impact factor: 5.917

  8 in total

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