Identification of a Maize Locus That Modulates the Hypersensitive Defense Response, Using Mutant-Assisted Gene Identification and Characterization

被引:45
作者
Chintamanani, Satya [3 ]
Hulbert, Scot H. [4 ]
Johal, Gurmukh S. [3 ]
Balint-Kurti, Peter J. [1 ,2 ]
机构
[1] N Carolina State Univ, USDA ARS, Plant Sci Res Unit, Raleigh, NC 27695 USA
[2] N Carolina State Univ, Dept Plant Pathol, Raleigh, NC 27695 USA
[3] Purdue Univ, Dept Bot & Plant Pathol, W Lafayette, IN 47907 USA
[4] Washington State Univ, Dept Plant Pathol, Pullman, WA 99164 USA
基金
美国国家科学基金会;
关键词
PR-LIKE PROTEIN; DISEASE RESISTANCE; MOLECULAR CHARACTERIZATION; NATURAL VARIATION; INNATE IMMUNITY; CELL-DEATH; ZEA-MAYS; RUST; EXPRESSION; ACCUMULATION;
D O I
10.1534/genetics.109.111880
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Potentially useful naturally occurring genetic variation is often difficult to identify as the effects of individual genes are subtle and difficult to observe. In this study, a novel genetic technique called Mutant-Assisted Gene Identification and Characterization is used to identify naturally occurring loci modulating the hypersensitive defense response (HR) in maize. Mutant-Assisted Gene Identification and Characterization facilitates the identification of naturally occurring alleles underlying phenotypic variation from diverse germplasm, using a mutant phenotype as a "reporter." In this study the reporter phenotype was caused by a partially dominant autoactive disease resistance gene, Rp1-D21, which caused HR lesions to form spontaneously all over the plant. Here it is demonstrated that the Rp1-D21 phenotype is profoundly affected by genetic background. By crossing the Rp1-D21 gene into the IBM mapping population, it was possible to map and identify Hrml1 on chromosome 10, a locus responsible for modulating the HR phenotype conferred by Rp1-D21. Other loci with smaller effects were identified on chromosomes 1 and 9. These results demonstrate that Mutant-Assisted Gene Identification and Characterization is a viable approach for identifying naturally occurring useful genetic variation.
引用
收藏
页码:813 / 825
页数:13
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