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Journal of Zhejiang University-SCIENCE B (Biomedicine & Biotechnology)  2009, Vol. 10 Issue (2): 112-119    DOI: 10.1631/jzus.B0820162
Biotechnology     
Clones identification of Sequoia sempervirens (D. Don) Endl. in Chile by using PCR-RAPDs technique
Manuel TORAL IBAÑEZ, Margarita CARU, Miguel A. HERRERA, Luis GONZALEZ, Luis M. MARTIN, Jorge MIRANDA, Rafael M. NAVARRO-CERRILLO
Department of Forest Management, Faculty of Forestry; Department of Ecological Sciences, Faculty of Sciences, University of Chile, Santa Rosa 11315, La Pintana, Santiago, Chile; Department of Forestry; Department of Genetic, School of Agriculture and Forestry, University of Córdoba, 14080 Córdoba, Spain
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Abstract  A protocol of polymerase chain reaction-random amplified polymorphic DNAs (PCR-RAPDs) was established to analyse the gene diversity and genotype identification for clones of Sequoia sempervirens (D. Don) Endl. in Chile. Ten (out of 34) clones from introduction trial located in Voipir-Villarrica, Chile, were studied. The PCR-RAPDs technique and a modified hexadecyltrimethylammonium bromide (CTAB) protocol were used for genomic DNA extraction. The PCR tests were carried out employing 10-mer random primers. The amplification products were detected by electrophoresis in agarose gels. Forty nine polymorphic bands were obtained with the selected primers (BG04, BF07, BF12, BF13, and BF14) and were ordered according to their molecular size. The genetic similarity between samples was calculated by the Jaccard index and a dendrogram was constructed using a cluster analysis of unweighted pair group method using arithmetic averages (UPGMA). Of the primers tested, 5 (out of 60) RAPD primers were selected for their reproducibility and high polymorphism. A total of 49 polymorphic RAPD bands were detected out of 252 bands. The genetic similarity analysis demonstrates an extensive genetic variability between the tested clones and the dendrogram depicts the genetic relationships among the clones, suggesting a geographic relationship. The results indicate that the RAPD markers permitted the identification of the assayed clones, although they are derived from the same geographic origin.

Key wordsSequoia sempervirens (D. Don) Endl.      Random amplified polymorphic DNAs (PCR-RAPDs)      Molecular markers      Clone assays      Chile      Genetic relationships     
Received: 05 May 2008     
CLC:  Q7  
Cite this article:

Manuel TORAL IBAÑEZ, Margarita CARU, Miguel A. HERRERA, Luis GONZALEZ, Luis M. MARTIN, Jorge MIRANDA, Rafael M. NAVARRO-CERRILLO. Clones identification of Sequoia sempervirens (D. Don) Endl. in Chile by using PCR-RAPDs technique. Journal of Zhejiang University-SCIENCE B (Biomedicine & Biotechnology), 2009, 10(2): 112-119.

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http://www.zjujournals.com/xueshu/zjus-b/10.1631/jzus.B0820162     OR     http://www.zjujournals.com/xueshu/zjus-b/Y2009/V10/I2/112

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