Clonal genetic diversity and populational genetic differentiation in Phragmites australis distributed in the Songnen Prairie in northeast China as revealed by amplified fragment length polymorphism and sequence-specific amplification polymorphism molecular markers

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dc.contributor.author Kimatu, Josphert N.
dc.contributor.author Li, M.
dc.contributor.author Gong, L.
dc.contributor.author Tian, Q.
dc.contributor.author Hu, L.
dc.contributor.author Guo, W.
dc.contributor.author Wang, D.
dc.contributor.author Liu, B.
dc.date.accessioned 2015-01-16T12:07:32Z
dc.date.available 2015-01-16T12:07:32Z
dc.date.issued 2009-02
dc.identifier.citation Annals of Applied Biology Volume 154, Issue 1, pages 43–55, February 2009 en_US
dc.identifier.issn 0003-4746
dc.identifier.uri http://onlinelibrary.wiley.com/doi/10.1111/j.1744-7348.2008.00269.x/pdf
dc.identifier.uri http://hdl.handle.net/123456789/594
dc.description DOI: 10.1111/j.1744-7348.2008.00269.x en_US
dc.description.abstract Genetic variation within and between four naturally occurring Phragmites australis land populations, DBS, QG, SS1 and SS2 (named after locality), which colonise distinct habitats (different edaphic conditions) in the Songnen Prairie in northeast China, were investigated by amplified fragment length polymorphism (AFLP) and sequence-specific amplification polymorphism (S-SAP) markers. It was found that the selected primer combinations of both markers were highly efficient in revealing the inter-clonal genetic diversity and inter-populational genetic differentiation in P. australis from a molecular ecological perspective. Cluster analysis categorised the plants into distinct groups (DBS, QG and SS groups), which were in line with their localities, albeit the two SS group populations (SS1 and SS2) showed a lower degree of inter-populational differentiation. These results were strongly supported by multiple statistical analysis including Mantel’s test, principal coordinate analysis, allocation test and analysis of molecular variance, which further suggested that gene flow, genetic drift and differences in as yet unidentified edaphic factors may all underpin the inter-clonal genetic diversity and inter-populational differentiation at the nucleotide sequence level. Analysis of intra-population clonal diversity also revealed that the QG population harboured a strikingly lower amount of within-population variation compared with those of the other three populations, presumably being caused by genetic drift and followed by physical and/or biological isolation. Homology analysis of a subset of population-specific or population-private AFLP and S-SAP bands suggested that regulatory genes and retroelements might play important roles in the ecological adaptation and differentiation of the P. australis populations. Possible causes for and implications of the extensive genetic variability in P. australis were discussed for its future genetic conservation and use in ecological revegetation. en_US
dc.language.iso en en_US
dc.publisher Association of Applied Biologists en_US
dc.subject Ecological adaptation en_US
dc.subject genetic diversity en_US
dc.subject molecular marker en_US
dc.subject Phragmites australis en_US
dc.subject population genetic differentiation en_US
dc.title Clonal genetic diversity and populational genetic differentiation in Phragmites australis distributed in the Songnen Prairie in northeast China as revealed by amplified fragment length polymorphism and sequence-specific amplification polymorphism molecular markers en_US
dc.type Article en_US


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