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水稻(Oryza sativa L.)中抗褐飞虱基因Bph15位点的高分辨率遗传图谱构建

High-resolution genetic mapping at the Bph15 locus for brown planthopper resistance in rice (Oryza sativa L.).

作者信息

Yang Haiyuan, You Aiqing, Yang Zhifan, Zhang Futie, He Ruifeng, Zhu Lili, He Guangcun

机构信息

Key Laboratory of Ministry of Education for Plant Development Biology, College of Life Sciences, Wuhan University, Wuhan 430072, China.

出版信息

Theor Appl Genet. 2004 Dec;110(1):182-91. doi: 10.1007/s00122-004-1844-0. Epub 2004 Nov 10.

Abstract

Resistance to the brown planthopper (BPH), Nilaparvata lugens Stal, a devastating sucking insect pest of rice, is an important breeding objective in rice improvement programs. Bph15, one of the 17 major BPH resistance genes so far identified in both cultivated and wild rice, has been identified in an introgression line, B5, and mapped on chromosome 4 flanked by restriction fragment length polymorphism markers C820 and S11182. In order to pave the way for positional cloning of this gene, we have developed a high-resolution genetic map of Bph15 by positioning 21 DNA markers in the target chromosomal region. Mapping was based on a PCR-based screening of 9,472 F(2) individuals derived from a cross between RI93, a selected recombinant inbred line of B5 bearing the resistance gene Bph15, and a susceptible variety, Taichung Native 1, in order to identify recombinant plants within the Bph15 region. Recombinant F(2) individuals with the Bph15 genotype were determined by phenotype evaluation. Analysis of recombination events in the Bph15 region delimited the gene locus to an interval between markers RG1 and RG2 that co-segregated with the M1 marker. A genomic library of B5 was screened using these markers, and bacterial artificial chromosome clones spanning the Bph15 chromosome region were obtained. An assay of the recombinants using the sub-clones of these clones in combination with sequence analysis delimited the Bph15 gene to a genomic segment of approximately 47 kb. This result should serve as the basis for eventual isolation of the Bph15 resistance gene.

摘要

褐飞虱(Nilaparvata lugens Stal)是水稻极具毁灭性的刺吸式害虫,培育抗褐飞虱的水稻品种是水稻改良计划中的重要育种目标。Bph15是迄今在栽培稻和野生稻中鉴定出的17个主要抗褐飞虱基因之一,已在渐渗系B5中鉴定出来,并定位在第4号染色体上,两侧是限制性片段长度多态性标记C820和S11182。为该基因的图位克隆铺平道路,我们通过在目标染色体区域定位21个DNA标记,构建了Bph15的高分辨率遗传图谱。图谱构建基于对9472个F2个体的PCR筛选,这些个体来自携带抗褐飞虱基因Bph15的B5选择重组自交系RI93与感病品种台中本地1号的杂交组合,目的是鉴定Bph15区域内的重组植株。通过表型评估确定具有Bph15基因型的重组F2个体。对Bph15区域重组事件的分析将基因座限定在与M1标记共分离的标记RG1和RG2之间的区间。使用这些标记筛选B5的基因组文库,获得了跨越Bph15染色体区域的细菌人工染色体克隆。使用这些克隆的亚克隆结合序列分析对重组体进行分析,将Bph15基因限定在约47 kb的基因组片段上。这一结果应为最终分离Bph15抗性基因奠定基础。

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