A comparison of molecular markers for genetic analysis of macadamia

被引:20
作者
Peace, CP
Vithanage, V
Neal, J
Turnbull, CGN
Carroll, BJ
机构
[1] CSIRO, Plant Ind, Queensland Biosci Project, Brisbane, Qld 4067, Australia
[2] Univ Queensland, Sch Land & Food Sci, Dept Biochem, Brisbane, Qld 4067, Australia
[3] Imperial Coll Wye, Dept Agr Sci, Ashford TN25 5AH, Kent, England
[4] Univ New England, Dept Ecosyst Management, Armidale, NSW 2351, Australia
关键词
D O I
10.1080/14620316.2004.11511874
中图分类号
S6 [园艺];
学科分类号
0902 ;
摘要
Various marker systems exist for genetic analysis of horticultural species. Isozymes were first applied to the woody perennial nut crop, macadamia, in the early 1990s. The advent of DNA markers saw the development, for macadamia, of STMS (sequence-tagged microsatellite site), RAPD (randomly amplified polymorphic DNA), and RAF (randomly amplified DNA fingerprinting). The RAF technique typically generates dominant markers, but within the dominant marker profiles, certain primers also amplify multi-allelic co-dominant markers that are suspected to be microsatellites. In this paper, we confirm this for one such marker, and describe how RAF primers can be chosen that amplify one or more putative microsatellites. This approach of genotyping anonymous microsatellite markers via RAF is designated RAMiFi (randomly amplified microsatellite fingerprinting). Several marker systems were compared for the type, amount, and cost-efficiency of the information generated, using data from published studies on macadamia. The markers were also compared for the way they clustered a common set of accessions. The RAMiFi approach was identified as the most efficient and economical. The availability of such a versatile tool offers many advantages for the genetic characterisation of horticultural species.
引用
收藏
页码:965 / 970
页数:6
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