https://www.ahs.ac.cn/images/0513-353X/images/top-banner1.jpg|#|苹果
https://www.ahs.ac.cn/images/0513-353X/images/top-banner2.jpg|#|甘蓝
https://www.ahs.ac.cn/images/0513-353X/images/top-banner3.jpg|#|菊花
https://www.ahs.ac.cn/images/0513-353X/images/top-banner4.jpg|#|灵芝
https://www.ahs.ac.cn/images/0513-353X/images/top-banner5.jpg|#|桃
https://www.ahs.ac.cn/images/0513-353X/images/top-banner6.jpg|#|黄瓜
https://www.ahs.ac.cn/images/0513-353X/images/top-banner7.jpg|#|蝴蝶兰
https://www.ahs.ac.cn/images/0513-353X/images/top-banner8.jpg|#|樱桃
https://www.ahs.ac.cn/images/0513-353X/images/top-banner9.jpg|#|观赏荷花
https://www.ahs.ac.cn/images/0513-353X/images/top-banner10.jpg|#|菊花
https://www.ahs.ac.cn/images/0513-353X/images/top-banner11.jpg|#|月季
https://www.ahs.ac.cn/images/0513-353X/images/top-banner12.jpg|#|菊花

园艺学报 ›› 2014, Vol. 41 ›› Issue (8): 1583-1590.

• 蔬菜 • 上一篇    下一篇

番茄抗黄化曲叶病毒基因Ty-1的双重SNP标记的开发

葛乃蓬,崔 龙,李汉霞,叶志彪*   

  1. (华中农业大学园艺植物生物学教育部重点实验室,武汉 430070)
  • 收稿日期:2014-05-19 出版日期:2014-08-25 发布日期:2014-08-25
  • 基金资助:
    国家现代农业产业技术体系建设专项资金项目(CARS-25-A-02);武汉市应用基础研究项目(2014020101010070,2013021702010584)

Double SNP Marker of Ty-1 Alleles in a Co-dominant Manner in Tomato

GE Nai-peng,CUI Long,LI Han-xia,and YE Zhi-biao*   

  1. (Key Laboratory of Horticultural Plant Biology,Ministry of Education,Huazhong Agricultural University,Wuhan 430070,China)
  • Received:2014-05-19 Online:2014-08-25 Published:2014-08-25

摘要: 本试验旨在开发一种新的设计共显性SNP标记的方法,以提高SNP标记检验的效率,并将其成功应用于番茄抗黄化曲叶病毒基因Ty-1的SNP标记开发中,提高了种质资源鉴定和育种分离世代材料筛选的效率。通过对抗病基因Ty-1和等位感病基因ty-1的cDNA序列进行比对,挑选了两个稳定扩增的多元非同义突变位点,分别用来设计Ty-1ty-1的SNP标记NL3和NL2,将两个标记进行混合得到双重SNP标记NL2-3。通过用NL2-3检验已知的抗病和感病番茄材料,验证了其多态性和稳定性。并用NL2-3对抗感病材料的F3代杂交分离群体和普通自交系进行了Ty-1的筛选,并经过田间观察进一步验证了该标记的可靠性。此方法开发得到的双重SNP标记只需要进行一次PCR反应和一次凝胶电泳就可以区分纯合抗、杂合抗、纯合感3种基因型,提高了育种选择的效率。

关键词: 番茄, 抗番茄黄化曲叶病基因, 双重SNP标记

Abstract: In this research,a novel method to develop co-dominant SNP markers which was called double SNP markers was developed. This new approach was used to obtain a double SNP marker named NL2-3 of Ty-1 gene resistant to TYLCV(Tomato yellow leaf curl virus)in tomato. The process of developing the NL2-3 double SNP marker included two main steps:Design specific primer pairs of resistant and susceptible genes individually based on two ideal SNP sites and mix the two specific primer pairs in one PCR reaction system with a proper ratio. With SNP marker NL2-3,we identified 5 resistant and 7 susceptible inbred lines and 3 homozygous Ty-1/Ty-1 resistant individuals,11 heterozygous Ty-1/ty-1 ones and 2 homozygous ty-1/ty-1 susceptible lines from F3 segregation population. This result was consistent with the field inoculation assay. We concluded that as the first double SNP marker of Ty-1 gene,NL2-3 can be directly applied to marker-assisted selection and would speed up the screening ofresistant breeding and cultivar evaluation.

Key words: tomato, Ty-1, double-SNP marker

中图分类号: