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利用突变体辅助基因鉴定和功能表征鉴定一个调节玉米过敏反应的基因。

Identification of a maize locus that modulates the hypersensitive defense response, using mutant-assisted gene identification and characterization.

机构信息

Department of Botany and Plant Pathology, Purdue University, West Lafayette, Indiana 47907-2054, USA.

出版信息

Genetics. 2010 Mar;184(3):813-25. doi: 10.1534/genetics.109.111880. Epub 2010 Feb 22.

Abstract

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.

摘要

潜在有用的自然发生遗传变异通常难以识别,因为单个基因的影响很细微,难以观察。在这项研究中,一种称为突变辅助基因鉴定和特征描述的新型遗传技术被用于鉴定调节玉米过敏反应防御反应(HR)的自然发生的调节位点。突变辅助基因鉴定和特征描述有助于从不同种质中鉴定出自然发生的等位基因,这些等位基因表现出表型变异,使用突变表型作为“报告基因”。在这项研究中,报告基因表型是由一个部分显性的自身激活疾病抗性基因 Rp1-D21 引起的,该基因导致 HR 病变在整个植物中自发形成。这里证明 Rp1-D21 表型受遗传背景的强烈影响。通过将 Rp1-D21 基因导入 IBM 图谱群体中,可以对 10 号染色体上的 Hrml1 进行作图和鉴定,该基因负责调节 Rp1-D21 赋予的 HR 表型。在 1 号和 9 号染色体上还鉴定到了其他具有较小影响的基因座。这些结果表明,突变辅助基因鉴定和特征描述是鉴定自然发生的有用遗传变异的一种可行方法。

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