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花生黄曲霉侵染抗性的SCAR标记 被引量:21

A SCAR Marker for Resistance to Aspergillus flavus in Peanut (Arachis hypogaea L.)
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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6.5cM。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。 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.
出处 《遗传》 CAS CSCD 北大核心 2006年第9期1107-1111,共5页 Hereditas(Beijing)
基金 国家自然科学基金项目(编号:30170561) 农业部油料作物遗传改良重点实验室开放课题(编号:200405)资助项目~~
关键词 花生 黄曲霉 分子标记 AFLP SCAR peanut (Arachis hypogaea L.) Aspergillus flavus molecular marker AFLP SCAR
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  • 1莫惠栋.数量遗传学的新发展——数量性状基因图谱的构建和应用[J].中国农业科学,1996,29(2):8-16. 被引量:50
  • 2翁曼丽,谢纬武,伏健民,王斌.新一代分子标记技术──AFLP[J].应用与环境生物学报,1996,2(4):424-429. 被引量:38
  • 3Valent B,Chumley F G.Molecular genetic analysis of the rice blast fungus,Magnaporthe grisea[J].Annu.Rev.Phytopathol, 1991, 29:443 - 467.
  • 4Dioh W, Tharreau D, Notteghem J L, et al. Mapping of avirulence genes in the rice blast fungus, Magnaporthe grisea, with RFLP and RAPD markers [J]. Mol. Plant Microbe Interact., 2000, 13(2):217-227.
  • 5Orbach M J,Leonard F,James A S,et al.A telomeric avirulence gene determines efficacy for the rice blast resistance gene Pita[J].Plant Cell, 2000, 12:2019-2032.
  • 6Farman M L, Leong S A. Chromosome walking to the AVRI-CO39 avirulence gene of Magnaporthe grisea: discrepancy between the physical and genetic maps [J]. Genetics, 1998, 150:1049-1058.
  • 7Paran I, Michelmore R W. Development of reliable PCR-based markers linked to downy mildew resistance genes in lettuce [ J]. Theor. Appl.Genet., 1993, 85:985-993.
  • 8Naqvi N 1, Chattoo B B. Development of a sequence characterized amplified resion (SCAR) based indirect selection method for a dominant blast-resistance gene in rice [J]. Genome, 1996, 39:26-30.
  • 9Hemandez P, Martin A, Dorado G. Development of SCARs by direct sequencing of RAPD products: a practical tool for the introgression and marker assisted selection of wheat[Jl. Molecular Breeding, 1999, 5:245 - 253.
  • 10Graham G C, Mayers P, Henry R J. A simplified method for the preparation of fungal genomic DNA for PCR and RAPD analysis [J]. Biotechnique, 1994, 16:48-50.

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