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一种基于聚合酶链式反应(PCR)的方法,用于从马铃薯中分离病原体抗性基因,具有在植物中广泛应用的潜力。

A PCR-based approach for isolating pathogen resistance genes from potato with potential for wide application in plants.

作者信息

Leister D, Ballvora A, Salamini F, Gebhardt C

机构信息

Max-Plank-Institut für Züchtungsforschung, Köln, Germany.

出版信息

Nat Genet. 1996 Dec;14(4):421-9. doi: 10.1038/ng1296-421.

Abstract

Plant genes for pathogen resistance can be used to engineer disease resistant crops. Oligonucleotides were designed from sequence motifs conserved between resistance genes of tobacco and Arabidopsis thaliana and used as PCR primers in potato DNA. Amplification products were obtained that were homologous to known resistance genes and linked without recombination with the nematode resistance locus Gro1 and the Phytophthora infestans resistance locus R7 of potato. Map positions of PCR-derived potato gene fragments were also correlated with resistance loci of the related tomato and tobacco genomes. Our results indicate that plant resistance genes that are effective against nematodes, fungi, viruses and bacteria may be isolated based on common sequence motifs and PCR methodology.

摘要

用于病原体抗性的植物基因可用于培育抗病作物。根据烟草和拟南芥抗性基因之间保守的序列基序设计寡核苷酸,并将其用作马铃薯DNA的PCR引物。获得了与已知抗性基因同源的扩增产物,并且这些产物与马铃薯的线虫抗性基因座Gro1和致病疫霉抗性基因座R7无重组地连锁。PCR衍生的马铃薯基因片段的图谱位置也与相关番茄和烟草基因组的抗性基因座相关。我们的结果表明,基于共同的序列基序和PCR方法,可以分离出对线虫、真菌、病毒和细菌有效的植物抗性基因。

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