Repetitive, genome-specific probes in wheat (Triticum aestivum) L em Thell amplified with minisatellite core sequences

被引:18
作者
Somers, DJ
Zhou, Z
Bebeli, PJ
Gustafson, JP
机构
[1] UNIV MISSOURI, PLANT SCI UNIT, DEPT AGRON, COLUMBIA, MO 65211 USA
[2] UNIV MISSOURI, USDA, AGR RES SERV, PLANT GENET RES UNIT, COLUMBIA, MO 65211 USA
[3] ATHENS AGR UNIV, DEPT PLANT BREEDING & BIOMETRY, ATHENS, GREECE
关键词
genome-specific; DAMD; minisatellite; PCR; Triticum; wheat;
D O I
10.1007/BF00224102
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
The detection and analysis of DNA polymorphisms in crops is an essential component of marker-assisted selection and cultivar identification in plant breeding. We have explored the direct amplification of minisatellite DNA by PCR (DAMD-PCR) as a means for generating DNA probes that are useful for detecting DNA polymorphisms and DNA fingerprinting in wheat. This technique was facilitated by high-stringency PCR with known plant and animal minisatellite core sequences as primers on wheat genomic DNA. The products of DAMD-PCR from Triticum aestivum, T. durum, T. monococcum, T. speltoides and T. tauschii showed a high degree of polymorphism and the various genomes could be identified. Cloning of the DAMD-PCR products and subsequent Southern hybridization frequently revealed polymorphic probes showing a good degree of genome specificity. In addition, polymorphic, single locus, and moderately dispersed PCR products were cloned that may have a potential for DNA fingerprinting. Our experiments were limited primarily to diploid wheats and the results indicated that DAMD-PCR may isolate genome-specific probes from wild diploid wheat species that could be used to monitor genome introgression into hexaploid wheat.
引用
收藏
页码:982 / 989
页数:8
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