用水稻抗白葉枯病基因Xa23的近等基因系CBB23與其感病輪回親本金剛30(JG30)雜交,構建了包含2562個單株的F2作圖群體.用水稻白葉枯病廣致病菌系P6進行抗性鑒定表明,F(xiàn)2植株抗感分離比嚴格符合3:1.根據(jù)日本水稻基因組計劃RGP水稻高密度圖譜上的RFLP探針對F2群體中的145個感病單株進行RFLP檢測和連鎖分析,獲得了6個與Xa23緊密連鎖的RFLP分子標記.其中RFLP標記C1003A靠著絲粒一側,與Xa23的遺傳圖距為0.4 cM,為Xa23的圖位克隆奠定了重要基礎.并將標記C1003A成功地轉化為STS標記,為分子標記輔助選擇育種(MAS)提供了方便有效的分子標記.
A F2 population derived from cross of the Xa23 near isogenic lines, JG30 and CBB23, was used for fine mapping of the ricebacterial blight resistance gene Xa23 1 Inoculation of the F2 plants with a Xanthomonas oryzae strain P6 showed a 3: 1 ratio for thesegregation of resistant and susceptible as expected1 One hundred and forty-five susceptible plants were selected from the F2 population formapping the gene Xa23 and fifteen restriction fragment length polymorphism ( RFLP) markers anchored on the rice high-density map1 ARFLP marker C1003A was found to be linked to the gene Xa23 by 014 cM1 This result constitutes an important basis for map-based cloningof the gene Xa231 The RFLP marker C1003A was transformed into sequence-tagged-site ( STS) marker, which can be applied for molecularmarke-r assisted selection (MAS) of Xa23 in rice breeding programs.