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Abstract
Polymerase chain reaction (PCR) primer pairs for 21 simple sequence repeat (SSR) loci in
Pinus strobus L, and 6 in
Pinus radiata D. Don were evaluated to determine whether SSR marker amplification could be achieved in 1O other conifer species. Eighty percent of SSR primer pairs for (AC) loci that were polymorphic in P.
strobus also amplified SSR loci in two other soft pines of the subgenus
Strobus but not in seven hard pines of the subgenus
Pinus nor in
Picea glauca (Moencb) Voss or Pseudotsuga
menziesii (Mirb.) Franco. The six P.
strobus SSR primer pairs that did amplify loci from conifers other than soft pines were those that were specific to loci monomorphic within P.
strobus. These six loci were also monomorphic within seven other species tested, but four of the loci were polymorphic among species. A comparison of allelic variation among the three soft pine species found only 25 shared alleles among a total of 122 alleles at eight loci. Primer pairs tbr dinucleotide SSR loci that were polymorphic in
Pinus radiata also specifically amplified loci from various other hard pines but not from the soft pines or from the other conifers tested.
Citation
Echt, C.S.; Vendramin, G.G.; Nelson, C. D.; Marquardt, Paula E. 1999. Microsatellite DNA as shared genetic markers among conifer species. Canadian Journal of Forest Research. 29: 365-371. (1999)