详细信息
Microsatellite-based Genotyping of the Commercial Eucalyptus Clones Cultivated in China ( SCI-EXPANDED收录) 被引量:6
文献类型:期刊文献
英文题名:Microsatellite-based Genotyping of the Commercial Eucalyptus Clones Cultivated in China
作者:Li, F.[1,2] Gan, S.[1,2] Zhang, Z.[3] Weng, Q.[1,2] Xiang, D.[3] Li, M.[1,2]
通信作者:Gan, S[1]
机构:[1]Chinese Acad Forestry, Res Inst Trop Forestry, Guangzhou 510520, Guangdong, Peoples R China;[2]Chinese Acad Forestry, Natl Key Lab Forest Tree Genet & Breeding, Guangzhou 510520, Guangdong, Peoples R China;[3]Guangxi Forestry Res Inst, Nanning 530001, Peoples R China
年份:2011
卷号:60
期号:5
起止页码:216-223
外文期刊名:SILVAE GENETICA
收录:;WOS:【SCI-EXPANDED(收录号:WOS:000300116300007)】;
基金:This work was financially supported by the National Program of High Technology Development of China (No. 2011AA100202) and Guangxi Academy of Forestry (GAF-Linke200907). The authors would like to thank DEYU GAN, CHANGFU HONG, JIANWEN LI and SHIRAO PENG for their kind help in sample collection.
语种:英文
外文关键词:Microsatellite; Eucalyptus clone; genotyping; genetic variation
摘要:A proper identification of clones is necessary in clonal forestry and will help to protect the legitimate interests of breeders, growers and industry. Twenty-four of the Eucalyptus clones most widely cultivated in China were analyzed using a set of 24 microsatellite markers to develop their DNA-based fingerprints and exploit the genetic variations. A total of 286 alleles were detected, averaging at 11.9 alleles per marker locus. All the microsatellites were polymorphic among the clones investigated. The observed heterozygosity (Ho) varied with locus between 0.500 and 1.000 with a mean of 0.885. The 24 clones could be uniquely fingerprinted based on their multilocus genotypes at a minimum of three loci (Embra169, Embra72 and Embra2). The dendrogram constructed from the genotypic similarity coefficients separated the 24 clones into three groups, matching essentially the historically known or speculated clonal origins. Clones T13, Guanglin-5 and Guanglin-9 turned out to be full siblings of cross DH32 while the DH201-2 sampled here appeared to be mislabelled.
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