Suitability of EST-PCR markers developed in highbush blueberry for genetic fingerprinting and relationship studies in lowbush blueberry and related species

Abstract

Little is known of the genetic structure and variability of wild fields, or of the dramatic differences in yield among clones (genetic individuals), of lowbush blueberry (Vaccinium angustifolium Ait.), Maine's most economically important fruit crop. Express sequence tag-polymerase chain reaction (EST-PCR) markers that were originally developed for genetic mapping purposes in highbush blueberry (Vaccinium corymbosum L.) are shown here to be valuable for genetic fingerprinting and relationship studies in the related species, V. angustifolium. As part of an interspecific genetic relationship study, 14 genotypes, including at least two specimens of each of four closely related Vaccinium L. species (V. pallidum Ait., V. corymbosum, V. boreale Hall & Aald., and V. myrtilloides Michx.) and the only four pedigreed cultivars of V. angustifolium, grouped out as expected in a genetic similarity dendrogram (matrix "r" correlation = 0.91). This work is ultimately aimed at using these markers in exploring how genetic relationship affects yield among proximal and distant breeding individuals via controlled field hand crosses. To help address this issue, a separate group of six individuals of V. angustifolium from two managed fields were also genotyped using the EST-PCR markers. The markers were very effective at intraspecific discrimination of individuals within the same field.