山西大学学报(自然科学版)
山西大學學報(自然科學版)
산서대학학보(자연과학판)
JOURNAL OF SHANXI UNIVERSITY
2009年
3期
455-462
,共8页
贺润丽%畅志坚%刘建霞%詹海仙%张晓军%董春林
賀潤麗%暢誌堅%劉建霞%詹海仙%張曉軍%董春林
하윤려%창지견%류건하%첨해선%장효군%동춘림
小麦%中间偃麦草%白粉病%基因定位%SSR
小麥%中間偃麥草%白粉病%基因定位%SSR
소맥%중간언맥초%백분병%기인정위%SSR
wheat%Thinopyrum intermedium%powdery mildew%gene mapping%SSR
CH5026是衍生于八倍体小偃麦TAI7045的新品系,用高感品种(系)CH5065、晋太170分别与CH5026配置组合,于温室接种并调查F_2、F_3、BC_1F_2群体的抗感分离之比进行遗传分析,结果表明CH5026成株期对白粉菌E09小种的抗性受1对显性基因控制,暂命名为PmCH5026.使用集群分离分析法(BSA),用378对SSR引物对CH5026×CH5065 F_2代群体进行分析,筛选到标记Xcfd233、Xbarc11和Xgwm539与抗性基因连锁,位置顺序为:Xcfd233-7.2cM-PmCH5026-4.9cM-Xbarc11-5.5cM-Xgwm539.根据小麦微卫星遗传连锁图及利用中国春第2同源群缺四体、双端体对SSR标记的定位结果,将PmCH5026定位在染色体2DL上.
CH5026是衍生于八倍體小偃麥TAI7045的新品繫,用高感品種(繫)CH5065、晉太170分彆與CH5026配置組閤,于溫室接種併調查F_2、F_3、BC_1F_2群體的抗感分離之比進行遺傳分析,結果錶明CH5026成株期對白粉菌E09小種的抗性受1對顯性基因控製,暫命名為PmCH5026.使用集群分離分析法(BSA),用378對SSR引物對CH5026×CH5065 F_2代群體進行分析,篩選到標記Xcfd233、Xbarc11和Xgwm539與抗性基因連鎖,位置順序為:Xcfd233-7.2cM-PmCH5026-4.9cM-Xbarc11-5.5cM-Xgwm539.根據小麥微衛星遺傳連鎖圖及利用中國春第2同源群缺四體、雙耑體對SSR標記的定位結果,將PmCH5026定位在染色體2DL上.
CH5026시연생우팔배체소언맥TAI7045적신품계,용고감품충(계)CH5065、진태170분별여CH5026배치조합,우온실접충병조사F_2、F_3、BC_1F_2군체적항감분리지비진행유전분석,결과표명CH5026성주기대백분균E09소충적항성수1대현성기인공제,잠명명위PmCH5026.사용집군분리분석법(BSA),용378대SSR인물대CH5026×CH5065 F_2대군체진행분석,사선도표기Xcfd233、Xbarc11화Xgwm539여항성기인련쇄,위치순서위:Xcfd233-7.2cM-PmCH5026-4.9cM-Xbarc11-5.5cM-Xgwm539.근거소맥미위성유전련쇄도급이용중국춘제2동원군결사체、쌍단체대SSR표기적정위결과,장PmCH5026정위재염색체2DL상.
Powdery mildew,caused by Blumeria graminis f. sp. tritici,is one of the most important diseases of wheat (Triticum aestivum L. ) worldwide and causes severe yield losses. Breeding for resistance is the most economical and effective method for controlling the disease. The wheat breeding line CH5026 derived from the partial wheat-Thinopyrum intermedium amphiploid TAI7045 is resistant to powdery mildew. To determine inheritance of powdery mildew resistance and map the resistance gene(s) in CH5026,F_2 ,F_3, BC_1F_2 progenies derived from the crosses of CH5026 with line CH5065 and susceptible cv. Jintai 170 were inoculated with Bgt isolate E09 in the greenhouse. Genetic analysis indicated that a single dominant gene, temporarily designated PmCH5026, was responsible for the resistance to Bgt in line CH5026. A total of 378 SSR markers were used to test the parents and resistant and susceptible bulks from the F_2 segregating population of CH5026 × CH5065. From the bulked segregant analysis,the polymorphic SSR markers were selected for genotyping the F_2 population. Three SSR markers Xcfd233 , Xbarc11 and Xgwm539 were identified to be linked to the resistance gene and their most likely order was Xcfd233,7. 2 cM, PmCH5026, 4.9 cM, Xbarc11 , 5. 5 cM, Xgwm539. Using the Chinese Spring nullisomic-tetrasomic and ditelosomic lines,the SSR markers mapped the resistance gene on chromosome arm 2DL.