Differentiating M. sativa ssp. sativa and ssp. falcata accessions using molecular markers

Patricia M. Cazcarro and E. Charles Brummer
Iowa State University, Ames, IA 50011

Cultivated alfalfa, Medicago sativa ssp. sativa, grown in most regions of the world owes few of its agronomic qualities to ssp. falcata. However, ssp. falcata possesses desirable cold, drought, and grazing tolerances (Oakley and Garver, 1917). Further, significant heterosis has been expressed in some sativa x falcata crosses (Wilsie, 1958; Sriwatanapongse and Wilsie, 1968). Several studies have shown falcata germplasm to be genetically distinct from sativa (Kidwell et al., 1994; Crochemore et al., 1996; Ghérardi et al., 1998). The objective of this experiment is to identify falcata accessions most distinct from sativa germplasm to guide development of improved falcata populations with complementary allelic structures to Midwestern U.S. breeding populations. We are examining putatively native accessions to study the geographical distribution of alfalfa diversity to guide germplasm enhancement efforts. The native ranges of falcata and sativa overlap to a considerable extent, but allopatric regions also occur: solely falcata grows in northern regions of Russia, Scandinavia, Mongolia, and China while sativa is the only subspecies in southern Europe, the Middle East, and Northern Africa (Ivanov, 1980; Lesins and Lesins, 1979). Ten accessions of each subspecies were selected from regions of coexistence and ten sativa and nine falcata accessions were selected from allopatric habitats, forming four "superpopulations" of sympatric sativa, sympatric falcata, allopatric sativa, and allopatric falcata. In addition to these 39, two M. prostrata accessions are included as an outgroup. Several types of molecular markers (RAPD, SSR, and RFLP) are being screened against two individuals of each accession. Genetic distances, calculated from the marker data, are used to cluster the various accessions. We are less interested in within population variation for this experiment, but rather in how the variation is structured over large geographical zones. Several questions will be discussed: Do sympatric and allopatric accessions form distinct clusters within each subspecies? Do sympatric accessions of each subspecies resemble each other more than they resemble their respective allopatric accessions? Though alfalfa populations contain considerable genetic diversity, significant differentiation among populations has also been reported (e.g Brummer et at., 1991). To get a clear picture of allelic differentiation among these accessions, a large number of polymorphic bands need to be screened. Results will be discussed relative to the usefulness of this method for detecting potentially useful germplasm.

References

Brummer, E.C., et al. 1991. Theor. Appl. Gen. 83:89-96.
Crochemore, M-L. et al. 1996. Agronomie 16:421-432.
Ghérardi, M. et al. 1998. Theor. Appl. Genet. 96:406-412.
Kidwell, K.K., et al. 1994. Crop Sci. 34:230-236.
Ivanov, A.I. 1988. Alfalfa. Translated by A.K. Dhote. Amerind Pub. Co. Pvt. Ltd., New Delhi.
Lesins, K. and I. Lesins. 1979. Genus Medicago (Leguminosae): A taxogenetic study. Kluwer, Dordrecht, The Netherlands.
Oakley, R.A. and S. Garver. 1917. USDA Bull. 428. U.S. Gov. Print. Office, Washington, D.C. 70 pp.
Sriwatanapongse, S. and C. P. Wilsie. 1968. Crop Sci. 8:465-466.
Wilsie, C.P. 1958. 16th Alfalfa Imp. Conf., Ithaca, NY. p. 21-33.

Previous Page