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ARS Home » Midwest Area » Madison, Wisconsin » Vegetable Crops Research » Research » Publications at this Location » Publication #188575


item Ipek, Meryem
item Ipek, Ahmet
item Simon, Philipp

Submitted to: Genome
Publication Type: Peer Reviewed Journal
Publication Acceptance Date: 7/12/2006
Publication Date: 12/20/2006
Citation: Ipek, M., Ipek, A., Simon, P.W. 2006. Sequence homology of polymorphic AFLP markers in garlic (Allium sativum l.). Genome. 49:1246-1255.

Interpretive Summary: The sequence of DNA is more similar among more related individuals or species, than among less related individuals or species. The process generating changes in DNA sequence is not well understood, so we evaluated short pieces of DNA, called AFLPs, in a diverse range of garlic clones to determine what type of DNA sequence variation has occurred and whether a pattern is evident. We observed a pattern of variation in DNA sequence of AFLPs that is very similar to the pattern of variation in plant morphology. This information is important to scientists interested in evaluating plant genetic differences, such as geneticists, and taxonomists, since it provides a rapid method for accurately evaluated relatedness among plants.

Technical Abstract: Linkage mapping and genetic diversity studies with randomly amplified polymorphic DNA (RAPD) or amplified fragment length polymorphisms (AFLP) markers in plant species have been carried out assuming that comigrating DNA bands are identical or at least have homologous sequences. To test this assumption in garlic, sequence identities of seven polymorphic AFLP markers from two selective amplification primer combinations previously used for similarity estimation in an earlier genetic diversity study were characterized. Among 37 diverse garlic clones, 87 bands from these seven polymorphisms were excised and 2 to 6 colonies were sequenced from each band to yield a total of 191 DNA inserts that were sequence characterized. All sequences contained expected nucleotide sequences of selective amplification primers indicating no error was introduced by AFLP amplification of amplicons due to the mismatches of nucleotides. Among 191 sequences, 124 independent AFLP amplicons were identified since 67 sequences had identical sequences with in a band. Of these 87 bands, 83 bands (95.4%) contained AFLP amplicons that were identical or highly homologous to the typical marker of that band while 4 bands contained one or more amplicons with little homology. Of these 83 bands, 64 (%73.6) contained only highly homologous (>90% sequence identity) and 19 (21.8%) contained both homologous and non-homologous amplicons. We found that 23 out of the 87 bands contained more than one amplicon, and that 37 (29.8%) of the 124 inserts from the 87 bands had non-homologous sequences with sequence identities less than 60%. Sequence conservation of AFLP amplicons followed patterns similar to phylogenetic relationships among garlic clones.