A next-generation sequencing method for overcoming the multiple gene copy problem in polyploid phylogenetics, applied to Poa grasses

BMC Biology

Methodology Article

Charles Robin¹  Philippa C Griffin¹  Ary A Hoffmann² 

[1] Department of Genetics, University of Melbourne, Parkville 3010, Victoria, Australia;Department of Genetics, University of Melbourne, Parkville 3010, Victoria, Australia;Department of Zoology, University of Melbourne, Parkville 3010, Victoria, Australia;

关键词: Nuclear Gene;    Spatial Genetic Structure;    Nuclear Region;    Incomplete Lineage Sorting;    Bacterial Cloning;   

DOI  :  10.1186/1741-7007-9-19

 received in 2011-03-01, accepted in 2011-03-23,  发布年份 2011

来源: Springer

【 摘 要 】

BackgroundPolyploidy is important from a phylogenetic perspective because of its immense past impact on evolution and its potential future impact on diversification, survival and adaptation, especially in plants. Molecular population genetics studies of polyploid organisms have been difficult because of problems in sequencing multiple-copy nuclear genes using Sanger sequencing. This paper describes a method for sequencing a barcoded mixture of targeted gene regions using next-generation sequencing methods to overcome these problems.ResultsUsing 64 3-bp barcodes, we successfully sequenced three chloroplast and two nuclear gene regions (each of which contained two gene copies with up to two alleles per individual) in a total of 60 individuals across 11 species of Australian Poa grasses. This method had high replicability, a low sequencing error rate (after appropriate quality control) and a low rate of missing data. Eighty-eight percent of the 320 gene/individual combinations produced sequence reads, and >80% of individuals produced sufficient reads to detect all four possible nuclear alleles of the homeologous nuclear loci with 95% probability.We applied this method to a group of sympatric Australian alpine Poa species, which we discovered to share an allopolyploid ancestor with a group of American Poa species. All markers revealed extensive allele sharing among the Australian species and so we recommend that the current taxonomy be re-examined. We also detected hypermutation in the trnH-psbA marker, suggesting it should not be used as a land plant barcode region. Some markers indicated differentiation between Tasmanian and mainland samples. Significant positive spatial genetic structure was detected at <100 km with chloroplast but not nuclear markers, which may be a result of restricted seed flow and long-distance pollen flow in this wind-pollinated group.ConclusionsOur results demonstrate that 454 sequencing of barcoded amplicon mixtures can be used to reliably sample all alleles of homeologous loci in polyploid species and successfully investigate phylogenetic relationships among species, as well as to investigate phylogeographic hypotheses. This next-generation sequencing method is more affordable than and at least as reliable as bacterial cloning. It could be applied to any experiment involving sequencing of amplicon mixtures.

【 授权许可】

CC BY   
© Griffin et al; licensee BioMed Central Ltd. 2011