Magnaporthe grisea pathogenicity genes obtained through insertional mutagenesis

被引:195
作者
Sweigard, JA
Carroll, AM
Farrall, L
Chumley, FG
Valent, B
机构
[1] DuPont Co Inc, Dept Cent Res & Dev, Wilmington, DE 19880 USA
[2] DuPont Co Inc, DuPont Agr Prod, Wilmington, DE 19880 USA
关键词
D O I
10.1094/MPMI.1998.11.5.404
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have initiated a mutational analysis of pathogenicity in the rice blast fungus, Magnaporthe grisea, in which hygromycin-resistant transformants, most generated by restriction enzyme-mediated integration (REMI), were screened for the ability to infect plants. A rapid primary infection assay facilitated screening of 5,538 transformants, Twenty-seven mutants were obtained that showed a reproducible pathogenicity defect, and 18 of these contained mutations that cosegregated with the hygromycin resistance marker. Analysis of eight mutants has resulted in the cloning of seven PTH genes that play a role in pathogenicity on barley, weeping lovegrass, and rice. Two independent mutants identified the same gene, PTH2, suggesting nonrandom insertion of the transforming DNA. These first 7 cloned PTH genes are described.
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收藏
页码:404 / 412
页数:9
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