黑龙江农业科学
黑龍江農業科學
흑룡강농업과학
HEILONGJINAG AGRICULTURAL SCIENCE
2012年
7期
1-5,18
,共6页
宋成艳%王桂玲%刘乃生%马文东%周雪松
宋成豔%王桂玲%劉迺生%馬文東%週雪鬆
송성염%왕계령%류내생%마문동%주설송
寒地%稻瘟病%菌系%抗性基因%累积分布曲线法
寒地%稻瘟病%菌繫%抗性基因%纍積分佈麯線法
한지%도온병%균계%항성기인%루적분포곡선법
cold region%rice blast%physiologic races%resistance gene%cumulative distribution curve method
为明确寒地核心种质抗病基因组成,利用日本7个单基因鉴别菌系(P-2b、研53-33、稻72、北1、研54-20、研54-04、稻168)接种鉴定了丽江新团黑谷×龙粳10号、丽江新团黑谷×垦稻10号组合10套F3系统,采用"累积分布曲线法"进行分析。结果表明:龙粳10号对P-2b、研53-33、稻72和北1四个菌系的抗性是由2对显性基因控制的,对研54-20的抗性是由3对显性基因控制的,对研54-04和稻168的抗性是由2对显性基因和1对隐性基因控制的。垦稻10号对研53-33的抗性基因是由2对显性基因控制的,对研54-20的抗性基因是由1对显性基因控制的,对研54-04的抗性是由2对显性互补基因控制。龙粳10号、垦稻10号可作为寒地水稻抗稻瘟病的核心种质,为抗病育种者选择亲本提供优质粳稻抗瘟源,并为寒地水稻核心种质库构建打下良好基础,在生产上应用具有重要意义。
為明確寒地覈心種質抗病基因組成,利用日本7箇單基因鑒彆菌繫(P-2b、研53-33、稻72、北1、研54-20、研54-04、稻168)接種鑒定瞭麗江新糰黑穀×龍粳10號、麗江新糰黑穀×墾稻10號組閤10套F3繫統,採用"纍積分佈麯線法"進行分析。結果錶明:龍粳10號對P-2b、研53-33、稻72和北1四箇菌繫的抗性是由2對顯性基因控製的,對研54-20的抗性是由3對顯性基因控製的,對研54-04和稻168的抗性是由2對顯性基因和1對隱性基因控製的。墾稻10號對研53-33的抗性基因是由2對顯性基因控製的,對研54-20的抗性基因是由1對顯性基因控製的,對研54-04的抗性是由2對顯性互補基因控製。龍粳10號、墾稻10號可作為寒地水稻抗稻瘟病的覈心種質,為抗病育種者選擇親本提供優質粳稻抗瘟源,併為寒地水稻覈心種質庫構建打下良好基礎,在生產上應用具有重要意義。
위명학한지핵심충질항병기인조성,이용일본7개단기인감별균계(P-2b、연53-33、도72、북1、연54-20、연54-04、도168)접충감정료려강신단흑곡×룡갱10호、려강신단흑곡×은도10호조합10투F3계통,채용"루적분포곡선법"진행분석。결과표명:룡갱10호대P-2b、연53-33、도72화북1사개균계적항성시유2대현성기인공제적,대연54-20적항성시유3대현성기인공제적,대연54-04화도168적항성시유2대현성기인화1대은성기인공제적。은도10호대연53-33적항성기인시유2대현성기인공제적,대연54-20적항성기인시유1대현성기인공제적,대연54-04적항성시유2대현성호보기인공제。룡갱10호、은도10호가작위한지수도항도온병적핵심충질,위항병육충자선택친본제공우질갱도항온원,병위한지수도핵심충질고구건타하량호기출,재생산상응용구유중요의의。
In order to make clear the genetic constitution of the resistance gene of the core genetic resources in cold region,10 F3 populations of Lijiangxintuanheigu×Longjing No.10 and Lijiangxintuanheigu×Kendao No.10 were inoculated by the seven single gene controlled strains(P-2b,Ken 53-33,Ina 72,Hoku 1,Ken54-20,Ken 54-04,Ina 168).Cumulative distribution curve method was applied.The results showed that the resistance of Longjing No.10 to P-2b,Ken 53-33,na 72 and Hoku 1 was controlled by 2 pairs dominant genes,to Ken 54-20 was controlled by 3 pairs dominant genes,to Ken 54-04 and Ina 168 was controlled by 2 pairs dominant genes and 1 pair recessive gene;that of Kendao No.10 to Ken 53-33 was controlled by 2 pairs dominant genes,to Ken 54-20 was controlled by 1 pair dominant gene,to Ken 54-04 was controlled by 2 pairs complementary dominant gene.Longjing No.10 and Kendao No.10 could be used as rice core germplasm of rice blast resistance in cold region to provide good rice blast resistance resource of parents selection for breeding,and made a good basis for building rice core germplasm bank in cold region and was important for rice production.