摘要
以感病材料10981为父本(P1),抗病材料10032为母本(P2),通过自交、杂交和回交,获得P1、P2两个亲本和F1、F2、BC1及BC2群体,接种鉴定各世代发病情况。选用288对Eco RⅠ/MseⅠ引物组合对P1、P2两个亲本,F1和F2代群体进行AFLP分析。卡方测验结果表明,抗源材料10032对黄化曲叶病毒的抗性表现为单基因显性遗传。经AFLP引物筛选及遗传连锁分析,获得与抗病基因Ty-3紧密连锁的标记E40/M49,遗传距离为3.4 cM。该研究可为番茄抗TYLCV分子标记辅助选择和抗TYLCV育种奠定基础。
Through hybridization, self crossing and back cross of the resistant parent P2 and susceptible parent P1, P1, F1(P1 × P2), F2, BC,, and BC2 were obtained. Plant disease incidence of all obtained generations was surveyed after artificial inoculation. AFLP analysis was conducted with 288 Eco R I/Mse I primer combinations on two parents P1, P2, F, and F2 generations of resistant and susceptible gene pool. The results showed that the generation of resistant and susceptible plants showed regular distribution. The Chi-square test results showed that yellow leaf curl virus resistance gene was one dominant gene in the resistant material P2. Genetic linkage analysis of the specific bands of AFLP markers and target gene was carried on in the F2 segregating population. The results showed that the specific bands E40/M49 was tightly linked to tomato yellow leaf curl virus resistant gene, and the genetic distance was 3.4 cM. This study would expedite the selection of tomato germplasm and could be used in TYLCV resistant breeding practice.
出处
《东北农业大学学报》
CAS
CSCD
北大核心
2014年第1期103-107,共5页
Journal of Northeast Agricultural University
基金
"十二五"国家支撑计划项目(2012BAD02B02-7)