遗传 ›› 2006, Vol. 28 ›› Issue (9): 1107-1111.

• 研究报告 • 上一篇    下一篇

花生黄曲霉侵染抗性的SCAR标记

雷 永1,2, 廖伯寿1, 王圣玉1, 张银波1,2, 李 栋1, 姜慧芳1   

  1. 1. 中国农业科学院油料作物研究所, 武汉 430062; 2. 农业部油料作物遗传改良重点实验室, 武汉 430062

  • 收稿日期:2005-09-16 修回日期:2006-01-09 出版日期:2006-09-01 发布日期:2006-09-01
  • 通讯作者: 雷永

A SCAR Marker for Resistance to Aspergillus flavus in Peanut (Ara-chis hypogaea L.)

LEI Yong1,2, LIAO Bo-Shou1, WANG Sheng-Yu1, ZHANG Yin-Bo1,2, LI Dong1, JIANG Hui-Fang1

  

  1. 1. Oil Crops Research Institute of Chinese Academy of Agricultural Sciences, Wuhan 430062, China; 2. Key Laboratory for Genetic Im-provement of Oil Crops of Ministry of Agriculture, Wuhan 430062, China

  • Received:2005-09-16 Revised:2006-01-09 Online:2006-09-01 Published:2006-09-01
  • Contact: LEI Yong

摘要: 利用与花生黄曲霉侵染抗性基因紧密连锁的AFLP标记 “E45/M53-440”, 经PAGE凝胶电泳后回收、克隆、测序, 并根据测序结果设计PCR特异引物, 通过对PCR条件的优化, 成功地将AFLP标记“E45/M53-440”转化为实验结果稳定, 操作更简单的SCAR标记“AFs-412”, 标记与花生黄曲霉侵染抗性间的遗传距离为6.5 cM。利用获得的SCAR标记对抗、感黄曲霉的花生种质资源进行了分子鉴定, 结果表明标记与抗性鉴定结果具有较高的一致性, 证实了该标记应用于研究群体之外的育种潜力。SCAR标记的建立为开展花生黄曲霉侵染抗性的标记辅助选择育种提供了简便实用的鉴定技术。

关键词: AFLP, SCAR, 分子标记, 黄曲霉, 花生

Abstract:

Aflatoxin contamination is an important constraint to peanut (Archis hypogaea L. ) industry worldwide. Genetic improvement for host resistance in peanut to fungal infection and aflatoxin (Aspergillus flavus) production is among the approaches for integrated management of the problem. However, the progress in peanut breeding for resistance to aflatoxin is slow due to various reasons, among which, lack of cost-effective method for resistance identification in breeding materials or segregating progenies has been encountered in most breeding programs. Hence there is a need to develop a rapid and reliable screening method for selecting A. flavus infection resistance in peanut. Here we report a SCAR (Sequence characterized Amplified Region) marker “AFs-412” converted from AFLP (amplified fragment length polymorphism) marker “E45/M53-440” which closely linked with resistance to A. flavus infection. Twenty peanut genotypes with resistance to infection of A. flavus were used to verify the reliability of the resistance markers, and high correlation between the molecular markers and the resistance result. The result shows that the potential of the markers which can be used in other resistant peanut genotypes to seed infection by Aspergillus flavus.

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