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作 者:马少芹[1] 许勇[2] 张海英[2] 宫国义[2] 沈火林[1]
机构地区:[1]中国农业大学农学与生物技术学院,北京100094 [2]国家蔬菜工程技术研究中心,北京100089
出 处:《植物病理学报》2006年第1期68-73,共6页Acta Phytopathologica Sinica
基 金:国家"八六三"资助项目(2001AA241174)
摘 要:小西葫芦黄花叶病毒中国株系(Zucchini yellow mosaic virus Chinese strain,ZYMV-CH)是危害我国四瓜的主要病毒。本实验以抗病毒病西瓜野生种质P.I.595203与感病的普通西瓜自交系98R为亲本,采用单粒传方式得到109个E3代株系,分别对亲本、F1及109个F3代株系群体进行了苗期抗ZYMV-CH接种鉴定,通过F3代群体的抗感分离情况,推测得到 F2代各单株的基因型,采用集团分离分析法(bulked segregant analysis,BSA)在F2代建立抗感基因池,以亲本、F1和抗感基因池为模板,对640条RAPD引物进行PCR扩增筛选,其中引物AK13在亲本、F1和抗感基因池之间扩增出一条多态性片段(644 bp),在F2代群体上验证该多态性条带与ZYMV-CH的抗性基因呈现连锁关系,遗传连锁距离为8 cM,定名为 AK13-644,该连锁标记在ZYMV-CH抗性转育后代自交系上得到了验证。最终将此RAPD标记成功转化成SCAR标记 SCAK13-644,该标记可以作为西瓜抗病毒病辅助选择的分子标记。Zucchini yellow mosaic virus Chinese strain (ZYMV-CH) is a major virus that causes severe losses in watermelon. The 109 lines of F3 derived from the single cross of the resistant wild germplasm P. I. 595203 and the susceptible inbred 98R were identified for their resistance to ZYMV-CH. The genotypes of 109 F2 individuals were assumed by the segregation of F3 population resistance. Using bulked segregant analysis (BSA), 640 RAPD primers were screened in resistant and susceptible parents, F1 and bulks. We found that a 644 bp fragment specifically amplified with RAPD primer AK13 which were present in P. I. 595203 and the resistant gene bulk but absent in 98R and the susceptible gene bulk. It was confirmed that the marker AK13-644 was linked to the gene resistant to ZYMV-CH in P. 1. 595203 by screening 109 F2 individuals and the linkage distance was 8 cM. The RAPD marker AK13-644 was confirmed in the introgressed resistant inbreds, and was transformed into SCAR marker SCAK13 -644 successfully. The result showed that this marker could be useful for marker-assisted selection in watermelon breeding for virus resistance.
分 类 号:S436.5[农业科学—农业昆虫与害虫防治]
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