Identification of molecular markers in soybean comparing RFLP, RAPD and AFLP DNA mapping techniques

被引:97
作者
Lin, JJ
Kuo, J
Ma, J
Saunders, JA
Beard, HS
MacDonald, MH
Kenworthy, W
Ude, GN
Matthews, BF
机构
[1] LIFE TECHNOL INC, GAITHERSBURG, MD 20877 USA
[2] USDA ARS, CLIMATE STRESS LAB, BELTSVILLE, MD 20705 USA
[3] USDA ARS, PLANT MOLEC BIOL LAB, BELTSVILLE, MD 20705 USA
[4] UNIV MARYLAND, DEPT AGRON, COLLEGE PK, MD 20742 USA
关键词
DNA fingerprinting; Glycine max; PCR;
D O I
10.1007/BF02684905
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Three different DNA mapping techniques-RFLP, RAPD and AFLP-were used on identical soybean germplasm to compare their ability to identify markers in the development of a genetic linkage map. Polymorphisms present in fourteen different soybean cultivars were demonstrated using all three techniques. AFLP, a novel PCR-based technique, was able to identify multiple polymorphic bands in a denaturing gel using 60 of 64 primer pairs tested. AFLP relies on primers designed in part on sequences for endonuclease restriction sites and on three selective nucleotides. The 60 diagnostic primer pairs tested for AFLP analysis each distinguished on average six polymorphic bands. Using specific primers designed for soybean from Eco RI and Mse I restriction site sequences and three selective nucleotides, as many as 12 polymorphic bands per primer could be obtained with AFLP techniques. Only 35 % of the RAPD reactions identified a polymorphic band using the same soybean cultivars, and in those positive reactions, typically only one or two polymorphic bands per gel were found. Identification of polymorphic bands using RFLP techniques was the most cumbersome, because Southern blotting and probe hybridization were required. Over 50 % of the soybean RFLP probes examined failed to distinguish even a single polymorphic band, and the RFLP probes that did distinguish polymorphic bands seldom identified more than one polymorphic band. We conclude that, among the three techniques tested, AFLP is the most useful.
引用
收藏
页码:156 / 169
页数:14
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