DNA amplification fingerprinting (DAF) with mini-hairpins harboring arbitrary 'core' sequences at their 3' termini were used to fingerprint a variety of templates, including PCR products and whole genomes, to establish genetic relationships between plant taxa at the interspecific and intraspecific level, and to identify closely related fungal isolates and plat accessions. No correlation was observed between the sequence of the arbitrary core, the stability of the mini-hairpin primers with short arbitrary cores and primers complementary to simple sequence repeats present in microsatellites were also used to generate arbitrary signatures from amplification procedure that uses at least one primer in each fingerprinting stage. ASAP was able to reproducibly amplify DAF products (representing about 10-15 kb of sequence) following careful optimization of amplification parameters such as primer and template concentration. Avoidance of primer sequences partially complementary to DAF product termini was necessary in order to produce distinct fingerprints. This allowed the combinatorial use of oligomers in nucleic acid screening, with numerous ASAP fingerprinting reactions based on a limited number of primer sequences. Mini-hairpin primers and ASAP analysis significantly increased detection of polymorphic DNA, separating closely related bermuda grass (Cynodon) cultivars and detecting putatively linked markers in bulked segregant analysis of the soybean (Glycine max) supernodulation (nitrate-tolerant symbiosis) locus.
|Original language||English (US)|
|Number of pages||13|
|State||Published - Jun 1996|
ASJC Scopus subject areas
- Biochemistry, Genetics and Molecular Biology(all)