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Mapping of Avirulence Genes in Phytophthora infestans With Amplified Fragment Length Polymorphism Markers Selected by Bulked Segregant Analysis
Author(s) -
Théo van der Lee,
Andrea V. Robold,
Antonino Testa,
John W. van't Klooster,
Francine Govers
Publication year - 2001
Publication title -
genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
eISSN - 1943-2631
pISSN - 0016-6731
DOI - 10.1093/genetics/157.3.949
Subject(s) - bulked segregant analysis , biology , phytophthora infestans , genetics , genetic linkage , amplified fragment length polymorphism , gene , positional cloning , gene mapping , oomycete , genetic marker , locus (genetics) , chromosome , population , demography , sociology , genetic diversity
In this study we investigated the genetic control of avirulence in the diploid oomycete pathogen Phytophthora infestans, the causal agent of late blight on potato. The dominant avirulence (Avr) genes matched six race-specific resistance genes introgressed in potato from a wild Solanum species. AFLP markers linked to Avr genes were selected by bulked segregant analysis and used to construct two high-density linkage maps, one containing Avr4 (located on linkage group A2-a) and the other containing a cluster of three tightly linked genes, Avr3, Avr10, and Avr11 (located on linkage group VIII). Bulked segregant analysis also resulted in a marker linked to Avr1 and this allowed positioning of Avr1 on linkage group IV. No bulked segregant analysis was performed for Avr2, but linkage to a set of random markers placed Avr2 on linkage group VI. Of the six Avr genes, five were located on the most distal part of the linkage group, possibly close to the telomere. The high-density mapping was initiated to facilitate future positional cloning of P. infestans Avr genes.

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