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通过代表性差异分析鉴定赋予水稻对褐飞虱(Nilaparvata lugens)抗性的候选基因。

The identification of candidate rice genes that confer resistance to the brown planthopper (Nilaparvata lugens) through representational difference analysis.

作者信息

Park Dong-Soo, Lee Sang-Kyu, Lee Jong-Hee, Song Min-Young, Song Song-Yi, Kwak Do-Yeon, Yeo Un-Sang, Jeon Nam-Soo, Park Soo-Kwon, Yi Gihwan, Song You-Chun, Nam Min-Hee, Ku Yeon-Chung, Jeon Jong-Seong

机构信息

Yeongnam Agricultural Research Institute, Milyang, 627-803, South Korea.

出版信息

Theor Appl Genet. 2007 Aug;115(4):537-47. doi: 10.1007/s00122-007-0587-0. Epub 2007 Jun 22.

Abstract

The development of rice varieties (Oryza sativa L.) that are resistant to the brown planthopper (BPH; Nilaparvata lugens Stål) is an important objective in current breeding programs. In this study, we generated 132 BC(5)F(5) near-isogenic rice lines (NILs) by five backcrosses of Samgangbyeo, a BPH resistant indica variety carrying the Bph1 locus, with Nagdongbyeo, a BPH susceptible japonica variety. To identify genes that confer BPH resistance, we employed representational difference analysis (RDA) to detect transcripts that were exclusively expressed in one of our BPH resistant NIL, SNBC61, during insect feeding. The chromosomal mapping of the RDA clones that we subsequently isolated revealed that they are located in close proximity either to known quantitative trait loci or to an introgressed SSR marker from the BPH resistant donor parent Samgangbyeo. Genomic DNA gel-blot analysis further revealed that loci of all RDA clones in SNBC61 correspond to the alleles of Samgangbyeo. Most of the RDA clones were found to be exclusively expressed in SNBC61 and could be assigned to functional groups involved in plant defense. These RDA clones therefore represent candidate defense genes for BPH resistance.

摘要

培育抗褐飞虱(BPH;Nilaparvata lugens Stål)的水稻品种(Oryza sativa L.)是当前育种计划的一个重要目标。在本研究中,我们通过将携带Bph1基因座的抗BPH籼稻品种三纲byeo与感BPH粳稻品种Nagdongbyeo进行五次回交,获得了132个BC(5)F(5)近等基因系(NILs)。为了鉴定赋予BPH抗性的基因,我们采用代表性差异分析(RDA)来检测在昆虫取食期间在我们的一个抗BPH NIL(SNBC61)中特异性表达的转录本。我们随后分离的RDA克隆的染色体定位显示,它们要么位于已知数量性状位点附近,要么位于来自抗BPH供体亲本三纲byeo的导入SSR标记附近。基因组DNA凝胶印迹分析进一步表明,SNBC61中所有RDA克隆的位点与三纲byeo的等位基因相对应。发现大多数RDA克隆仅在SNBC61中表达,并可归类为参与植物防御的功能组。因此,这些RDA克隆代表了抗BPH的候选防御基因。

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