PCR-amplified microsatellites as markers in plant genetics

✍ Scribed by M. Morgante; A.M. Olivieri

• Publisher: John Wiley and Sons
• Year: 1993
• Tongue: English
• Weight: 906 KB
• Volume: 3
• Category: Article
• ISSN: 0960-7412
• DOI: 10.1046/j.1365-313x.1993.t01-9-00999.x

✦ Synopsis

Summary

In order to assess the feasibility of using microsatellites as markers in plant genetics, a survey of published DNA sequence data for presence, abundance and ubiquity in higher plants of all types of dinucleotide and trinucleotide repeats with a minimum number of 10 and 7 units, respectively, was conducted. This search revealed that such microsatellites are frequent and widely distributed; they were uncovered in 34 species, with a frequency of one every 50 kb. AT repeats were by far the most frequently observed class of dinucleotide microsatellites, whereas AC/TG repeats, which are common in animals, were observed only once. TAT repeats prevailed among trinucleotides. Polymerase chain reaction amplification of (AT)~n~ and (TAT)~n~ micro‐satellites in soybean (Glycine max (L.) Merr.) revealed that they are highly polymorphic, as a consequence of length variation, somatically stable and inherited in a co‐dominant Mendelian manner. The abundance and amount of information derived from such markers, together with the ease by which they can be identified, make them ideal markers for plant genetic linkage and physical mapping, population studies and varietal identification.