Western white pine SNP discovery and high-throughput genotyping for breeding and conservation applications

BMC Plant Biology

Research Article

Jun-Jun Liu¹  Hao Chen¹  Rona N Sturrock¹  Richard A Sniezko² 

[1] Pacific Forestry Centre, Canadian Forest Service, Natural Resources Canada, 506 West Burnside Road, V8Z 1M5, Victoria, BC, Canada;USDA Forest Service, Dorena Genetic Resource Center, 34963 Shoreview Road, 97424, Cottage Grove, OR, USA;

关键词: Five-needle pine;    Genotyping array;    Linkage disequilibrium;    Marker-based selection;    Pedigree reconstruction;   

DOI  :  10.1186/s12870-014-0380-6

 received in 2014-03-31, accepted in 2014-12-11,  发布年份 2014

来源: Springer

【 摘 要 】

BackgroundWestern white pine (WWP, Pinus monticola Douglas ex D. Don) is of high interest in forest breeding and conservation because of its high susceptibility to the invasive disease white pine blister rust (WPBR, caused by the fungus Cronartium ribicola J. C. Fisch). However, WWP lacks genomic resource development and is evolutionarily far away from plants with available draft genome sequences. Here we report a single nucleotide polymorphism (SNP) study by bulked segregation-based RNA-Seq analysis.ResultsA collection of resistance germplasm was used for construction of cDNA libraries and SNP genotyping. Approximately 36–89 million 2 × 100-bp reads were obtained per library and de-novo assembly generated the first shoot-tip reference transcriptome containing a total of 54,661 unique transcripts. Bioinformatic SNP detection identified >100,000 high quality SNPs in three expressed candidate gene groups: Pinus highly conserved genes (HCGs), differential expressed genes (DEGs) in plant defense response, and resistance gene analogs (RGAs). To estimate efficiency of in-silico SNP discovery, genotyping assay was developed by using Sequenom iPlex and it unveiled SNP success rates from 40.1% to 61.1%. SNP clustering analyses consistently revealed distinct populations, each composed of multiple full-sib seed families by parentage assignment in the WWP germplasm collection. Linkage disequilibrium (LD) analysis identified six genes in significant association with major gene (Cr2) resistance, including three RGAs (two NBS-LRR genes and one receptor-like protein kinase -RLK gene), two HCGs, and one DEG. At least one SNP locus provided an excellent marker for Cr2 selection across P. monticola populations.ConclusionsThe WWP shoot tip transcriptome and those validated SNP markers provide novel genomic resources for genetic, evolutionary and ecological studies. SNP loci of those candidate genes associated with resistant phenotypes can be used as positional and functional variation sites for further characterization of WWP major gene resistance against C. ribicola. Our results demonstrate that integration of RNA-seq-based transcriptome analysis and high-throughput genotyping is an effective approach for discovery of a large number of nucleotide variations and for identification of functional gene variants associated with adaptive traits in a non-model species.

【 授权许可】

CC BY   
© Liu et al.; licensee BioMed Central. 2014