分子植物育种
分子植物育種
분자식물육충
MOLECULAR PLANT BREEDING
2013年
2期
232-240
,共9页
王神云%曹家树%余小林%黄建新%李建斌*
王神雲%曹傢樹%餘小林%黃建新%李建斌*
왕신운%조가수%여소림%황건신%리건빈*
结球甘蓝%霜霉病%抗霜霉病基因%AFLP标记%SCAR标记
結毬甘藍%霜黴病%抗霜黴病基因%AFLP標記%SCAR標記
결구감람%상매병%항상매병기인%AFLP표기%SCAR표기
Headed cabbage%Downy mildew (Hyaloperonospora parasitica)%Downy mildew resistant gene%AFLP marker%SCAR marker
结球甘蓝霜霉病是由十字花科寄生霜霉菌引发的严重病害.本研究利用高代自交系‘R103’抗病亲本和‘S101’感病亲本及其F2分离群体,于霜霉病病发高峰期田间自然诱发抗性鉴定,由单基因显性控制.运用AFLP分子标记技术,结合BSA法,对双亲和2对抗、感基因池的筛选和验证,获得2个与结球甘蓝抗霜霉病基因相关的AFLP标记.204 bp BoRAAC/CAC标记转化为SCAR标记,发现在抗病亲本和抗病池中与感病亲本和感病池中条带只存在量上的差异,在抗性选择起中只能起辅助作用;191 bp BoRAAG/CTC标记(EU-635443.1),转化为SCAR标记,仅在抗病亲本和2个抗病池中获得目的条带,经F2群体单株验证后,与抗性位点的遗传距离为5.7 cM.利用BoRAAG/CTC113标记对F1和BC1群体与多年苗期霜霉病抗性鉴定的20份结球甘蓝种质资源进行验证和筛选,该标记与品种(系)的霜霉病抗性吻合率达到95%,初步表明该标记可应用于早期结球甘蓝抗霜霉病抗性辅助选择.
結毬甘藍霜黴病是由十字花科寄生霜黴菌引髮的嚴重病害.本研究利用高代自交繫‘R103’抗病親本和‘S101’感病親本及其F2分離群體,于霜黴病病髮高峰期田間自然誘髮抗性鑒定,由單基因顯性控製.運用AFLP分子標記技術,結閤BSA法,對雙親和2對抗、感基因池的篩選和驗證,穫得2箇與結毬甘藍抗霜黴病基因相關的AFLP標記.204 bp BoRAAC/CAC標記轉化為SCAR標記,髮現在抗病親本和抗病池中與感病親本和感病池中條帶隻存在量上的差異,在抗性選擇起中隻能起輔助作用;191 bp BoRAAG/CTC標記(EU-635443.1),轉化為SCAR標記,僅在抗病親本和2箇抗病池中穫得目的條帶,經F2群體單株驗證後,與抗性位點的遺傳距離為5.7 cM.利用BoRAAG/CTC113標記對F1和BC1群體與多年苗期霜黴病抗性鑒定的20份結毬甘藍種質資源進行驗證和篩選,該標記與品種(繫)的霜黴病抗性吻閤率達到95%,初步錶明該標記可應用于早期結毬甘藍抗霜黴病抗性輔助選擇.
결구감람상매병시유십자화과기생상매균인발적엄중병해.본연구이용고대자교계‘R103’항병친본화‘S101’감병친본급기F2분리군체,우상매병병발고봉기전간자연유발항성감정,유단기인현성공제.운용AFLP분자표기기술,결합BSA법,대쌍친화2대항、감기인지적사선화험증,획득2개여결구감람항상매병기인상관적AFLP표기.204 bp BoRAAC/CAC표기전화위SCAR표기,발현재항병친본화항병지중여감병친본화감병지중조대지존재량상적차이,재항성선택기중지능기보조작용;191 bp BoRAAG/CTC표기(EU-635443.1),전화위SCAR표기,부재항병친본화2개항병지중획득목적조대,경F2군체단주험증후,여항성위점적유전거리위5.7 cM.이용BoRAAG/CTC113표기대F1화BC1군체여다년묘기상매병항성감정적20빈결구감람충질자원진행험증화사선,해표기여품충(계)적상매병항성문합솔체도95%,초보표명해표기가응용우조기결구감람항상매병항성보조선택.
@@@@Downy mildew caused by the oomycete Hyaloperonospora parasitica Constant. (Pers. Ex Fr.) is a serious threat to Brassicaceae family. In this study, the resistance was conferred by a single dominant gene of F2 young adults, gotten from high inbred lines‘R103’ resistant parent and‘S101’ susceptible parent, on the disease peak stage in field. AFLP technology was applied to identify the markers linked to downy mildew resistant locus based on BSA method. Two resistant AFLP markers were obtained from the parents and two pairs of pools, which constructed from F2 plants. The 204 bp marker BoRAAC/CAC, which has been converted to SCAR marker, indicated the quantitive difference, so it is only for resistance selection diminutively. Whereas, the 191 bp marker BoRAAG/CTC (Accessment number:EU635443.1), which has been converted to the SCAR marker, was only obtained from the resistant parent and pools, and the genetic distance between the downy mildew resistant gene is 5.7 cM verified by F2 plants. In addition, the F1 and BC1 population had verified the accuracy of the SCAR marker BoRAAG/CTC113, and 20 materials also had verified its accuracy, the reistance consistency was 95%. These results demonstrated that the BoRAAG/CTC113 provided a basis SCAR marker for resistance identified and marker assisted breeding in headed cabbage.