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Open Access Research article

Enhancing genetic mapping of complex genomes through the design of highly-multiplexed SNP arrays: application to the large and unsequenced genomes of white spruce and black spruce

Nathalie Pavy1*, Betty Pelgas12, Stéphanie Beauseigle1, Sylvie Blais1, France Gagnon1, Isabelle Gosselin1, Manuel Lamothe12, Nathalie Isabel12 and Jean Bousquet1

Author Affiliations

1 Arborea and Canada Research Chair in Forest and Environmental Genomics, Centre d'Étude de la Forêt, Pavillon Charles-Eugène-Marchand, Université Laval, Québec, Québec G1V 0A6, Canada

2 Natural Resources Canada, Canadian Forest Service, Laurentian Forestry Centre, 1055 Rue du P.E.P.S., C.P. 10380, succ. Saint-Foy, Québec, Québec G1V 4C7, Canada

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BMC Genomics 2008, 9:21  doi:10.1186/1471-2164-9-21

Published: 18 January 2008

Abstract

Background

To explore the potential value of high-throughput genotyping assays in the analysis of large and complex genomes, we designed two highly multiplexed Illumina bead arrays using the GoldenGate SNP assay for gene mapping in white spruce (Picea glauca [Moench] Voss) and black spruce (Picea mariana [Mill.] B.S.P.).

Results

Each array included 768 SNPs, identified by resequencing genomic DNA from parents of each mapping population. For white spruce and black spruce, respectively, 69.2% and 77.1% of genotyped SNPs had valid GoldenGate assay scores and segregated in the mapping populations. For each of these successful SNPs, on average, valid genotyping scores were obtained for over 99% of progeny. SNP data were integrated to pre-existing ALFP, ESTP, and SSR markers to construct two individual linkage maps and a composite map for white spruce and black spruce genomes. The white spruce composite map contained 821 markers including 348 gene loci. Also, 835 markers including 328 gene loci were positioned on the black spruce composite map. In total, 215 anchor markers (mostly gene markers) were shared between the two species. Considering lineage divergence at least 10 Myr ago between the two spruces, interspecific comparison of homoeologous linkage groups revealed remarkable synteny and marker colinearity.

Conclusion

The design of customized highly multiplexed Illumina SNP arrays appears as an efficient procedure to enhance the mapping of expressed genes and make linkage maps more informative and powerful in such species with poorly known genomes. This genotyping approach will open new avenues for co-localizing candidate genes and QTLs, partial genome sequencing, and comparative mapping across conifers.