Journal of Resources and Ecology ›› 2020, Vol. 11 ›› Issue (5): 466-474.DOI: 10.5814/j.issn.1674-764x.2020.05.004

• Forest Ecosystem • Previous Articles     Next Articles

Genetic Diversity of Toona ciliata Populations based on SSR Markers

WANG Yang, YUE Dan*(), LI Xinzhi*()   

  1. Hubei Ecology Polytechnic College, Wuhan 430200, China
  • Received:2020-02-19 Accepted:2020-06-03 Online:2020-09-30 Published:2020-09-30
  • Contact: YUE Dan,LI Xinzhi
  • Supported by:
    Foundation: The Public Welfare Research Project of Department of Science and Technology in Hubei Province(402012DBA40001);The Scientific Research Project of Department of Education in Hubei Province(B20160555)


In order to provide a theoretical basis for the protection and development of T. ciliata germplasm resources, we studied the genetic diversity of T. ciliata by using SSR (Simple Sequence Repeat) primers to evaluate the genetic diversity of 192 T. ciliata germplasm samples from 24 populations of 5 provinces. DataFormater, Popgene, NTSYS, TFPGA and other software were used for genetic data conversion, genetic parameter estimation, dendrogram construction and genetic variation analysis. The results showed that: 1) a total of 17 alleles (Na) were detected in seven pairs of primers, with an average of 2.260 for each primer. Among them, the highest numbers of alleles (4) were detected in primers S11 and S422.The mean value of Nei’s genetic diversity index (H) was 0.4909, the mean value of Shannon information index (I) was 0.7321, and the mean value of polymorphic information content (PIC) was 0.5182. The mean expected heterozygosity (He) and observed heterozygosity (Ho) were 0.1055 and 0.4956, respectively. The Nei°s genetic distances of the populations ranged between 0.0002 and 2.6346, and the mean was 0.5477. The average genetic diversity level (H=0.1044) of the 24 populations was lower than that of the species (H=0.4909). 2) The genetic differentiation coefficients (Fst) varied from 0.2374 to 0.9148, with an average value of 0.7727. The mean of population gene flow (Nm) was 0.0735, indicating a low level of genetic exchange between populations, and suggesting that the genetic variation mainly came from within populations. 3) With the UPGMA method, the 24 populations were clustered into 3 groups at Nei’s genetic identity (0.99): the populations from Guizhou Province and Guangxi Zhuang Autonomous Region were clustered into one group, the populations from Hunan Province were in another group, and the populations from Hubei Province were in the third group. The Mantel test analysis showed a significant correlation between Nei’s genetic distance and geographic distance (r=0.6318, P=0.009?0.05). The genetic diversity of the 24 populations of T. ciliata was at a low level. Geographic isolation was the main reason for genetic differentiation among T. ciliata provenances. In the protection of germplasm resources of T. ciliata, emphasis should be placed on breeding genetic resources from the populations with higher genetic diversity (P14, for example). As for the populations with low genetic diversity, an ex-situ protection strategy as well as ecological and timber objectives, should be taken into account to maximize the conservation and utilization of the diversity of T. ciliata.

Key words: Toona ciliata, SSR marker, natural population, genetic diversity, genetic differentiation