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Citation:

Genetic Diversity of Allozyme Markers of Liquidambar formosana Hance

  • Received Date: 2011-04-24
  • The leaf samples from 16 Liquidambar formosana Hance populations were analyzed to study allozyme diversity using vertical slab polyacrylamide gel electrophoresis, and 6 loci of 6 enzyme systems were recorded. The results showed:(1) The genetic structures were different among populations. Allele frequencies ranged from 0-1.00, 4 rare genes and 3 unique genes were found in the assayed populations. At least 1 rare gene was found in 9 populations and 1 unique gene in 6 populations. (2) At species level, the mean number of alleles per locus was 3, the mean number of effective alleles per locus was 1.855 7, the percentage of polymorphic loci was 100%, and the observed heterozygosity was 0.582, the expected heterozygosity was 0.443, the mean value of Shannon index was 0.711 0. Overall, the proportion of heterozygotes within these populations was excessive. (3) According to the UPGMA cluster analysis based on Nei's genetic distance, the populations were classified into two groups, the Jian'ou population was clearly separated from all other populations by a large distance from other populations, and the rest 15 populations forming a big group, in which the populations of Fengdu and Huangshan were more distant from the other 13 populations, and genetic distances among the 13 populations were smaller from each other. The grouping of populations by cluster analysis was generally in consistence with the pattern of geographic distribution of the populations.
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Genetic Diversity of Allozyme Markers of Liquidambar formosana Hance

  • 1. State Key Laboratory of Tree Genetics and Breeding, Research Institute of Forestry, Chinese Academy of Forestry, Beijing 100091, China
  • 2. Nanjing Forestry University, Nanjing 210037, Jiangsu, China
  • 3. Center for Forest Tree Breeding, Hubei Provincial Forestry Bureau, Wuhan 430079, Hubei, China

Abstract: The leaf samples from 16 Liquidambar formosana Hance populations were analyzed to study allozyme diversity using vertical slab polyacrylamide gel electrophoresis, and 6 loci of 6 enzyme systems were recorded. The results showed:(1) The genetic structures were different among populations. Allele frequencies ranged from 0-1.00, 4 rare genes and 3 unique genes were found in the assayed populations. At least 1 rare gene was found in 9 populations and 1 unique gene in 6 populations. (2) At species level, the mean number of alleles per locus was 3, the mean number of effective alleles per locus was 1.855 7, the percentage of polymorphic loci was 100%, and the observed heterozygosity was 0.582, the expected heterozygosity was 0.443, the mean value of Shannon index was 0.711 0. Overall, the proportion of heterozygotes within these populations was excessive. (3) According to the UPGMA cluster analysis based on Nei's genetic distance, the populations were classified into two groups, the Jian'ou population was clearly separated from all other populations by a large distance from other populations, and the rest 15 populations forming a big group, in which the populations of Fengdu and Huangshan were more distant from the other 13 populations, and genetic distances among the 13 populations were smaller from each other. The grouping of populations by cluster analysis was generally in consistence with the pattern of geographic distribution of the populations.

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