Development of microsatellite markers in cultivated and wild species of sections Cepa and Phyllodolon in Allium
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The potential of microsatellite markers for use in genetic studies has been evaluated in Allium cultivated species (Allium cepa, A. fistulosum) and its allied species (A. altaicum, A. galanthum, A. roylei, A. vavilovii). A total of 77 polymerase chain reaction (PCR) primer pairs were employed, 76 of which amplified a single product or several products in either of the species. The 29 AMS primer pairs derived from A. cepa and 46 microsatellites primer pairs from A. fistulosum revealed a lot of polymorphic amplicons between seven Allium species. Some of the microsatellite markers were effective not only for identifying an intraspecific F1 hybrid between shallot and bulb onion but also for applying to segregation analyses in its F2 population. All of the microsatellite markers can be used for interspecific taxonomic analyses among two cultivated and four wild species of sections Cepa and Phyllodolon in Allium. Generally, our data support the results obtained from recently performed analyses using molecular and morphological markers. However, the phylogeny of A. roylei, a threatened species with several favorable genes, was still ambiguous due to its different positions in each dendrogram generated from the two primer sets originated from A. cepa and A. fistulosum.
KeywordsAllium Microsatellite markers DNA polymorphism
The authors wish to thank Misses N. Yamane, N. Matsubara, Y. Kousabara and M. Anraku (former students in Yamaguchi University) together with Messrs Y. Kosaka and S. Hasegawa (present students in YU) for their technical contributions to this study. The authors are grateful to Dr. C. Kik and Mr. W. Wietsma in PRI for the kind gift of wild species. The Polymorphic examinations were supported in part by a funding for ‘Research project for utilizing advanced technologies in agriculture, forestry and fisheries’ from the Ministry of Agriculture, Forestry and Fisheries of Japan, and segregation analyses by a Grant-in-Aid for Scientific Research (C) (No. 15580025) from the Ministry of Education, Science, Sports, and Culture of Japan.
- Felsenstein J (1989) PHYLIP—Phylogeny Inference Package (version 3.2). Cladistics 5:164–166Google Scholar
- Havey M (1995) Onion and other cultivated alliums. In: Smartt J, Simmonds NW (eds) Evolution of crop plants, 2nd edn. Longman Scientific and Technical, Burnt Mill, pp 344–350Google Scholar
- Kuhl JC, Cheung F, Yuan Q, Martin W, Zewdie Y, McCallum J, Catanach A, Rutherford P, Sink KC, Jenderek M, Prince JP, Town CD, Havey MJ (2004) A unique set of 11,008 onion expressed sequence tags reveals expressed sequence and genomic differences between the monocot orders Asparagales and Poales. Plant Cell 16:114–125CrossRefPubMedGoogle Scholar
- Lacy ML, Lorbeer JW (2008) Botrytis leaf blight. In: Schwartz HF, Mohan SK (eds) Compendium of onion and garlic diseases and pests, 2nd edn. The American Phytopathological Society Press, Minnesota, pp 26–29Google Scholar
- Masuzaki S, Araki N, Yamauchi N, Yamane N, Wako T, Kojima A, Shigyo M (2006) Chromosomal locations of microsatellites in onion. HortScience 41:315–318Google Scholar
- McCallum J (2007) Onion. In: Kole C (ed) Genome mapping and molecular breeding in plants, vol 5: vegetables. Springer-Verlag, Berlin, pp 331–347Google Scholar
- Schwartz HF (2008) Downy mildew. In: Schwartz HF, Mohan SK (eds) Compendium of onion and garlic diseases and pests, 2nd edn. The American Phytopathological Society Press, Minnesota, pp 32–35Google Scholar
- Sulistyaningsih E, Tashiro Y, Shigyo M, Isshiki S (1997) Morphological and cytological characteristics of haploid shallot. Bull Fac Agric Saga Univ 82:7–15Google Scholar
- Vvedensky A (1944) The genus Allium in the USSR. Herbertia 11:65–218Google Scholar
- Wako T, Ohara T, Song YS, Kojima A (2002) Development of SSR markers in bunching onion. Breed Res 4(Suppl 1):83 (in Japanese)Google Scholar