No retraction, correction or concern found when last checked on Oct 29, 2026.
Scanning the genome for gene single nucleotide polymorphisms involved in adaptive population differentiation in white spruce
MARIE‐CLAIRE NAMROUD, JEAN BEAULIEU, NICOLAS JUGE and 2 more
Molecular Ecology · 2008
doi:10.1111/j.1365-294x.2008.03840.x
Abstract
Conifers are characterized by a large genome size and a rapid decay of linkage disequilibrium, most often within gene limits. Genome scans based on noncoding markers are less likely to detect molecular adaptation linked to genes in these species. In this study, we assessed the effectiveness of a genome‐wide single nucleotide polymorphism (SNP) scan focused on expressed genes in detecting local adaptation in a conifer species. Samples were collected from six natural populations of white spruce ( Picea glauca ) moderately differentiated for several quantitative characters. A total of 534 SNPs representing 345 expressed genes were analysed. Genes potentially under natural selection were identified by estimating the differentiation in SNP frequencies among populations ( F ST ) and identifying outliers, and by estimating local differentiation using a Bayesian approach. Both average expected heterozygosity and population differentiation estimates ( H E = 0.270 and F ST = 0.006) were comparable to those obtained with other genetic markers. Of all genes, 5.5% were identified as outliers with F ST at the 95% confidence level, while 14% were identified as candidates for local adaptation with the Bayesian method. There was some overlap between the two gene sets. More than half of the candidate genes for local adaptation were specific to the warmest population, about 20% to the most arid population, and 15% to the coldest and most humid higher altitude population. These adaptive trends were consistent with the genes’ putative functions and the divergence in quantitative traits noted among the populations. The results suggest that an approach separating the locus and population effects is useful to identify genes potentially under selection. These candidates are worth exploring in more details at the physiological and ecological levels.
Shown for reading. Its publisher allows quoting it, not republishing it.
References 92
- 1.
Acheré V, Favre JM, Besnard G, Jeandroz S. Genomic organization of molecular differentiation in Norway spruce (Picea abies. Molecular Ecology. 2005;14:3191-3201.
Not in our library10.1111/j.1365-294x.2005.02646.x
- 2.
Akey JM, Zhang G, Zhang K, Jin L, Shriver MD. Interrogating a high-density SNP map for signatures of natural selection. Genome Research. 2002;12:1805-1814.
Not in our library10.1101/gr.631202
- 3.
Altshuler D, Pollara VJ, Cowles CR, et al. An SNP map of the human genome generated by reduced representation shotgun sequencing. Nature. 2000;407:513-516.
Not in our library10.1038/35035083
- 4.
Andalo C, Beaulieu J, Bousquet J. The impact of climate change on growth of local white spruce populations in Québec, Canada. Forest Ecology and Management. 2005;205:169-182.
Not in our library
- 5.
Beaty TH, Fallin MD, Hetmanski JB, et al. Haplotype diversity in 11 candidate genes across four populations. Genetics. 2005;171:259-267.
Not in our library10.1534/genetics.105.043075
- 6.
Beaumont MA, Balding DJ. Identifying adaptive genetic divergence among populations from genome scans. Molecular Ecology. 2004;13:969-980.
Not in our library10.1111/j.1365-294x.2004.02125.x
- 7.
Beaumont MA, Nichols RA. Evaluating loci for use in the genetic analysis of population structure. Proceedings of the Royal Scoiety B: Biological Sciences. 1996;263:1619-1626.
Not in our library
- 8.
Bedon F, Grima-Pettenati J, Mackay J. Conifer R2R3-MYB transcription factors: sequence analyses and gene expression in wood-forming tissues of white spruce (Picea glauca. BMC Plant Biology. 2007;7:17.
Not in our library10.1186/1471-2229-7-17
- 9.
Bonin A, Taberlet P, Miaud C, Pompanon F. Explorative genome scan to detect candidate loci for adaptation along a gradient in the common frog (Rana temporaria. Molecular Biology and Evolution. 2006;23:773-783.
Not in our library10.1093/molbev/msj087
- 10.
Bouck A, Vision T. The molecular ecologist's guide to expressed sequence tag. Molecular Ecology. 2007;16:909-924.
Not in our library10.1111/j.1365-294x.2006.03195.x
- 11.
Bousquet J, Isabel N, Pelgas B, Kole C, et al. Spruce. Forest Trees. 2007;Vol. 7:93-114.
Not in our library
- 12.
Bradshaw HDJ, Schemske DW. Allele substitution at a flower colour locus produces a pollinator shift in monkey flowers. Nature. 2003;426:176-178.
Not in our library10.1038/nature02106
- 13.
Brem RB, Yvert G, Clinton R, Kruglyak L. Genetic dissection of transcriptional regulation in budding yeast. Science. 2002;296:752-755.
Not in our library10.1126/science.1069516
- 14.
Broderick P, Carvajal-Carmona L, Webb E, et al. A genome–wide association study shows that common alleles of SMAD7 influence colorectal cancer risk. Nature Genetics. 2007;39:1315-1317.
Not in our library10.1038/ng.2007.18
- 15.
Brown GR, Gill GP, Kuntz RJ, Langley CH, Neale D. Nucleotide diversity and linkage disequilibrium in loblolly pine. Proceedings of the National Academy of Sciences, USA. 2004;101:15255-15260.
Not in our library10.1073/pnas.0404231101
- 16.
Brumfield RT, Beerli P, Nickerson DA, Edwards SV. The utility of single nucleotide polymorphisms in inferences of population history. Trends in Ecology and Evolution. 2003;18:249-256.
Not in our library
- 17.
Campbell D, Bernatchez L. Generic scan using AFLP markers as a means to assess the role of directional selection in the divergence of sympatric whitefish ecotypes. Molecular Biology and Evolution. 2004;21:945-956.
Not in our library10.1093/molbev/msh101
- 18.
Carmel L, Wolf YI, Rogozin IB, Koonin EV. Three distinct modes of intron dynamics in the evolution of eukaryotes. Genome Research. 2007;17:1034-1044.
Not in our library10.1101/gr.6438607
- 19.
Chamary JV, Hurst LD. Similar rates but different modes of sequence evolution in introns and at exonic silent sites in rodents: evidence for selectively driven codon usage. Molecular Biology and Evolution. 2004;21:1014-1023.
Not in our library10.1093/molbev/msh087
- 20.
Ching A, Caldwell K, Jung M, et al. SNP frequency, haplotype structure and linkage disequilibrium in elite maize inbred lines. BMC Genetics. 2002;3:19.
Not in our library10.1186/1471-2156-3-19
- 21.
Corcuera L, Camarero JJ, Gil-Pelegrín E. Effects of a severe drought on growth and wood anatomical properties of Quercus Faginea. IAWA Journal. 2004;25:185-204.
Not in our library
- 22.
Cork JM, Purugganan MD. High-diversity genes in the Arabidopsis genome. Genetics. 2005;170:1897-1911.
Not in our library10.1534/genetics.104.036152
- 23.
Drake JA, Bird C, Nemesh J, et al. Conserved noncoding sequences are selectively constrained and not mutation cold spots. Nature Genetics. 2005;38:223-227.
Not in our library10.1038/ng1710
- 24.
Erickson DL, Fenster CB, Stenoien HK, Price D. Quantitative trait locus analyses and the study of evolutionary process. Molecular Ecology. 2004;13:2505-2522.
Not in our library10.1111/j.1365-294x.2004.02254.x
- 25.
Fan JB, Oliphant A, Shen R, et al. Highly parallel SNP genotyping. Cold Spring Harbor Symposia on Quantitative Biology. 2003;69-78.
Not in our library10.1101/sqb.2003.68.69
- 26.
Ford MJ. Applications of selective neutrality tests to molecular ecology. Molecular Ecology. 2002;11:1245-1262.
Not in our library10.1046/j.1365-294x.2002.01536.x
- 27.
Frank AC, Lobry JR. Asymmetric substitution patterns: a review of possible underlying mutational or selective mechanisms. Gene. 1999;238:65-77.
Not in our library10.1016/s0378-1119(99)00297-8
- 28.
Frewen BE, Chen THH, Howe GT, et al. Quantitative trait loci and candidate gene mapping of bud set and bud flush in Populus. Genetics. 2000;154:837-845.
Not in our library10.1093/genetics/154.2.837
- 29.
Gazave E, Marqués-Bonet T, Fernando O, Charlesworth B, Navarro A. Patterns and rates of intron divergence between humans and chimpanzees. Genome Biology. 2007;8:R21.
Not in our library10.1186/gb-2007-8-2-r21
- 30.
Glazier AM, Nadeau JH, Aitman TJ. Finding genes that underlie complex traits. Science. 2002;298:2345-2349.
Not in our library10.1126/science.1076641
- 31.
Godt MJW, Hamrick MA, Edwards-Burke MA, Williams JH. Comparisons of genetic diversity in white spruce (Picea glauca) and jack pine (Pinus banksiana) seed orchards with natural populations. Canadian Journal of Forest Research. 2001;31:943-949.
Not in our library
- 32.
- 33.
Hassett DJ, Cohen MS. Bacterial adaptation to oxidative stress: implications for pathogenesis and interaction with phagocytic cells. The Federation of American Societies for Experimental Biology. 1989;3:2574-2582.
Not in our library10.1096/fasebj.3.14.2556311
- 34.
Hedrick PW. Perspective: highly variable loci and their interpretation in evolution and conservation. Evolution. 1999;53:313-318.
Not in our library10.1111/j.1558-5646.1999.tb03767.x
- 35.
Heidelberger P, Welch P. Spectral method for confidence interval generation and run length control in simulations. Communications of the ACM. 1981;24:233-245.
Not in our library
- 36.
Howe GT, Aitken SN, Neale DB, et al. From genotype to phenotype: unravelling the complexities of cold adaptation in forest trees. Canadian Journal of Botany. 2003;81:1247-1266.
Not in our library
- 37.
Hurme P, Sillanpaa MJ, Arjas E, Repo T, Savolainen O. Genetic basis of climatic adaptation in Scots pine by Bayesian quantitative trait locus analysis. Genetics. 2000;156:1309-1322.
Not in our library10.1093/genetics/156.3.1309
- 38.
- 39.
Isabel N, Beaulieu J, Bousquet J. Complete congruence between gene diversity estimates derived from genotypic data at enzyme and RAPD loci in black spruce. Proceedings of the National Academy of Sciences, USA. 1995;92:6369-6373.
Not in our library10.1073/pnas.92.14.6369
- 40.
Isabel N, Beaulieu J, Theriault P, Bousquet J. Direct evidence for biased gene diversity estimates from dominant random amplified polymorphic DNA (RAPD) fingerprints. Molecular Ecology. 1999;8:477-483.
Not in our library
Cited by papers we hold 6
- Characterization of Global Transcriptome Using Illumina Paired-End Sequencing and Development of EST-SSR Markers in Two Species of Gynostemma (Cucurbitaceae) · 2015Not checked
- Characterisation of adaptive genetic diversity in environmentally contrasted populations of Eucalyptus camaldulensis Dehnh. (river red gum). · 2014Not checked
- Potential for evolutionary responses to climate change – evidence from tree populations · 2013No notice
- Characterization of the sesame (Sesamum indicum L.) global transcriptome using Illumina paired-end sequencing and development of EST-SSR markers · 2011No notice
- Transcriptome sequencing in an ecologically important tree species: assembly, annotation, and marker discovery · 2010No notice
- Genomic signatures of local directional selection in a high gene flow marine organism; the Atlantic cod (Gadus morhua) · 2009No notice
Reads
Read by people on this page
None yet.
Checked or read by AI through naulon
None yet.
A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.
Are you an author?
Is this your paper?
Claim it to add your note and be paid when agents cite it. Free.