中国农业科学
中國農業科學
중국농업과학
SCIENTIA AGRICULTURA SINICA
2015年
8期
1484-1491
,共8页
杨慧勇%赵文博%王花云%张福耀
楊慧勇%趙文博%王花雲%張福耀
양혜용%조문박%왕화운%장복요
高粱%丝黑穗病%抗性基因%基因定位
高粱%絲黑穗病%抗性基因%基因定位
고량%사흑수병%항성기인%기인정위
sorghum%head smut%resistance gene%gene mapping
【目的】对高粱的丝黑穗病菌4号生理小种抗性基因进行定位分析,筛选与抗病基因连锁的分子标记,为抗丝黑穗病育种奠定基础。【方法】以对高粱丝黑穗病菌1、2、3、4号生理小种均表现免疫的材料961541为母本,以对1、2、3号生理小种免疫、对4号生理小种感病的材料V4B及高感材料PI550607为父本,进行杂交,构建F2群体。采用菌土法在播种时进行田间接种,抽穗后对抗/感亲本、F1及F2群体材料进行发病率调查。利用微卫星分子标记技术(SSR)和分离群体分组分析法(BSA)对961541/V4B的F2群体进行抗病基因的定位分析。【结果】961541/V4B组合中,抗病亲本961541发病率为0,感病亲本V4B发病率为21.5%,F1发病率为0,F2群体发病率为7.25%;961541/PI550607组合中,高感亲本PI550607的发病率为64.81%,F1及F2群体发病率分别为0和5%。适合性检验表明,2个组合的F2群体的抗、感病株比率均符合15﹕1(χ2=0.201、0.322,P>0.05),4号生理小种的抗病性受2对非等位基因控制。所试274对SSR引物中共有53对引物在抗、感亲本间存在差异。利用筛选出的53对引物进一步对抗、感池进行特异引物筛选,仅位于高粱第1染色体上的SSR引物Xtxp325在抗、感池间表现差异。其中,抗池与免疫材料961541的带型一致,感池与鉴别寄主V4B的带型一致;选取5对引物(Xtxp325、Xtxp302、Xtxp32、Xtxp340和Xtxp248)进行连锁图谱构建,构建的连锁图谱全长355.3 cM,4号生理小种抗性基因Shs1与Xtxp325之间的遗传距离为27.7 cM。【结论】高粱丝黑穗病菌4号生理小种的抗病性受2对非等位基因控制。构建的连锁图谱全长355.3 cM,与发表的连锁图谱有较好的对应关系,高粱丝黑穗病菌4号生理小种抗病基因位于第1染色体上,Shs1与Xtxp325的遗传距离为27.7 cM。
【目的】對高粱的絲黑穗病菌4號生理小種抗性基因進行定位分析,篩選與抗病基因連鎖的分子標記,為抗絲黑穗病育種奠定基礎。【方法】以對高粱絲黑穗病菌1、2、3、4號生理小種均錶現免疫的材料961541為母本,以對1、2、3號生理小種免疫、對4號生理小種感病的材料V4B及高感材料PI550607為父本,進行雜交,構建F2群體。採用菌土法在播種時進行田間接種,抽穗後對抗/感親本、F1及F2群體材料進行髮病率調查。利用微衛星分子標記技術(SSR)和分離群體分組分析法(BSA)對961541/V4B的F2群體進行抗病基因的定位分析。【結果】961541/V4B組閤中,抗病親本961541髮病率為0,感病親本V4B髮病率為21.5%,F1髮病率為0,F2群體髮病率為7.25%;961541/PI550607組閤中,高感親本PI550607的髮病率為64.81%,F1及F2群體髮病率分彆為0和5%。適閤性檢驗錶明,2箇組閤的F2群體的抗、感病株比率均符閤15﹕1(χ2=0.201、0.322,P>0.05),4號生理小種的抗病性受2對非等位基因控製。所試274對SSR引物中共有53對引物在抗、感親本間存在差異。利用篩選齣的53對引物進一步對抗、感池進行特異引物篩選,僅位于高粱第1染色體上的SSR引物Xtxp325在抗、感池間錶現差異。其中,抗池與免疫材料961541的帶型一緻,感池與鑒彆寄主V4B的帶型一緻;選取5對引物(Xtxp325、Xtxp302、Xtxp32、Xtxp340和Xtxp248)進行連鎖圖譜構建,構建的連鎖圖譜全長355.3 cM,4號生理小種抗性基因Shs1與Xtxp325之間的遺傳距離為27.7 cM。【結論】高粱絲黑穗病菌4號生理小種的抗病性受2對非等位基因控製。構建的連鎖圖譜全長355.3 cM,與髮錶的連鎖圖譜有較好的對應關繫,高粱絲黑穗病菌4號生理小種抗病基因位于第1染色體上,Shs1與Xtxp325的遺傳距離為27.7 cM。
【목적】대고량적사흑수병균4호생리소충항성기인진행정위분석,사선여항병기인련쇄적분자표기,위항사흑수병육충전정기출。【방법】이대고량사흑수병균1、2、3、4호생리소충균표현면역적재료961541위모본,이대1、2、3호생리소충면역、대4호생리소충감병적재료V4B급고감재료PI550607위부본,진행잡교,구건F2군체。채용균토법재파충시진행전간접충,추수후대항/감친본、F1급F2군체재료진행발병솔조사。이용미위성분자표기기술(SSR)화분리군체분조분석법(BSA)대961541/V4B적F2군체진행항병기인적정위분석。【결과】961541/V4B조합중,항병친본961541발병솔위0,감병친본V4B발병솔위21.5%,F1발병솔위0,F2군체발병솔위7.25%;961541/PI550607조합중,고감친본PI550607적발병솔위64.81%,F1급F2군체발병솔분별위0화5%。괄합성검험표명,2개조합적F2군체적항、감병주비솔균부합15﹕1(χ2=0.201、0.322,P>0.05),4호생리소충적항병성수2대비등위기인공제。소시274대SSR인물중공유53대인물재항、감친본간존재차이。이용사선출적53대인물진일보대항、감지진행특이인물사선,부위우고량제1염색체상적SSR인물Xtxp325재항、감지간표현차이。기중,항지여면역재료961541적대형일치,감지여감별기주V4B적대형일치;선취5대인물(Xtxp325、Xtxp302、Xtxp32、Xtxp340화Xtxp248)진행련쇄도보구건,구건적련쇄도보전장355.3 cM,4호생리소충항성기인Shs1여Xtxp325지간적유전거리위27.7 cM。【결론】고량사흑수병균4호생리소충적항병성수2대비등위기인공제。구건적련쇄도보전장355.3 cM,여발표적련쇄도보유교호적대응관계,고량사흑수병균4호생리소충항병기인위우제1염색체상,Shs1여Xtxp325적유전거리위27.7 cM。
[Objective]The objective of this study is to conduct mapping genes conferring resistance to physiological race 4 of head smut disease in sorghum and screen the molecular markers linked to the resistance genes, in order to lay a foundation for sorghum resistance breeding against the head smut in future.[Method]To build F2 populations, the material 961541 as a female, which is immune to physiological races 1, 2, 3, and 4, was crossed with V4B which is immune to physiological races 1, 2, and 3 and sensitive to race 4 and PI550607 which is sensitive to physiological races 1, 2, 3, and 4. The seeds were inoculated with soil containing suitable chlamydospores at sowing time, and the disease incidence of the parents, F1 progenies and F2 population was investigated at heading stage. The localization of resistance gene was studied by SSR technology and bulked segregation analysis (BSA) method using the 961541/V4B population.[Result]The results of field investigation showed that, for the cross combination 961541/V4B, the morbidities of 961541 and the F1 progeny both were 0, and that of V4B and F2 population were 21.5%and 7.25%, respectively. For another cross combination 961541/PI550607, the morbidities of PI550607 was 64.81%, and that of the F1 progeny, F2 population were 0 and 5%, respectively. The fitness test indicated that, for the two F2 populations, the ratio of resistance quantities to sensitive quantities both were conformed to 15:1(χ2=0.201, 0.322, P>0.05), which implied that the resistance genes to head smut race 4 should be controlled by 2 non-allelic genes. The linkage analysis showed that, among the total 274 pairs of SSR primers, 53 pairs showed different amplification between the parents. Then screening of the specificity primers among the 53 pairs were conducted between the resistance pool and the sensitive pool, while only Xtxp325 on chromosome 1 was specific. The banding pattern of resistance pool was the same as 961541, and the sensitive pool was as the material V4B. Linkage mapping with the 5 pairs primers (Xtxp325, Xtxp302, Xtxp32, Xtxp340, Xtxp248) showed that the overall length of linkage map was 355.3 cM, the genetic distance between Xtxp325 and the resistance gene (Shs1) was 27.7 cM.[Conclusion]The resistances to physiological race 4 of sorghum head smut might be controlled by two mutual independent non-allelic genes. The linkage map was good correspondence with the public maps, and which the overall length was 355.3 cM. The resistance gene Shs1 of head smut race 4 is located on No. 1 chromosome of sorghum, and the genetic distance is 27.7 cM from the primer Xtxp325.