Genomic prediction accuracies in space and time for height and wood density of Douglas-fir using exome capture as the genotyping platform
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články
PubMed
29197325
PubMed Central
PMC5712148
DOI
10.1186/s12864-017-4258-5
PII: 10.1186/s12864-017-4258-5
Knihovny.cz E-zdroje
- Klíčová slova
- Douglas-fir, Exome capture, Full-sib families, Genomic selection, Genotype x environment interaction, Predictive model,
- MeSH
- dřevo chemie genetika MeSH
- exom * MeSH
- genomika MeSH
- genotyp MeSH
- lineární modely MeSH
- lokus kvantitativního znaku MeSH
- modely genetické * MeSH
- Pseudotsuga genetika růst a vývoj MeSH
- selekce (genetika) * MeSH
- šlechtění rostlin * MeSH
- vysoce účinné nukleotidové sekvenování MeSH
- Publikační typ
- časopisecké články MeSH
BACKGROUND: Genomic selection (GS) can offer unprecedented gains, in terms of cost efficiency and generation turnover, to forest tree selective breeding; especially for late expressing and low heritability traits. Here, we used: 1) exome capture as a genotyping platform for 1372 Douglas-fir trees representing 37 full-sib families growing on three sites in British Columbia, Canada and 2) height growth and wood density (EBVs), and deregressed estimated breeding values (DEBVs) as phenotypes. Representing models with (EBVs) and without (DEBVs) pedigree structure. Ridge regression best linear unbiased predictor (RR-BLUP) and generalized ridge regression (GRR) were used to assess their predictive accuracies over space (within site, cross-sites, multi-site, and multi-site to single site) and time (age-age/ trait-trait). RESULTS: The RR-BLUP and GRR models produced similar predictive accuracies across the studied traits. Within-site GS prediction accuracies with models trained on EBVs were high (RR-BLUP: 0.79-0.91 and GRR: 0.80-0.91), and were generally similar to the multi-site (RR-BLUP: 0.83-0.91, GRR: 0.83-0.91) and multi-site to single-site predictive accuracies (RR-BLUP: 0.79-0.92, GRR: 0.79-0.92). Cross-site predictions were surprisingly high, with predictive accuracies within a similar range (RR-BLUP: 0.79-0.92, GRR: 0.78-0.91). Height at 12 years was deemed the earliest acceptable age at which accurate predictions can be made concerning future height (age-age) and wood density (trait-trait). Using DEBVs reduced the accuracies of all cross-validation procedures dramatically, indicating that the models were tracking pedigree (family means), rather than marker-QTL LD. CONCLUSIONS: While GS models' prediction accuracies were high, the main driving force was the pedigree tracking rather than LD. It is likely that many more markers are needed to increase the chance of capturing the LD between causal genes and markers.
Zobrazit více v PubMed
Hayes B, Bowman P, Chamberlain A, Goddard M. Genomic selection in dairy cattle: progress and challenges. J Dairy Sci. 2009;92:433–443. doi: 10.3168/jds.2008-1646. PubMed DOI
Grattapaglia D. Breeding forest trees by genomic selection: current progress and the way forward. In: Tuberosa R, et al., editors. Genomics of plant genetic resources. Netherlands: Springer; 2014. p. 651–82.
Lorenz AJ, Chao S, Asoro FG, Heffner EL, Hayashi T, Iwata H, Smith KP, Sorrells MK, Jannink JL. Genomic selection in plant breeding: knowledge and prospects. Adv Agron. 2011;110:77. doi: 10.1016/B978-0-12-385531-2.00002-5. DOI
Fisher RA. The correlation between relatives on the supposition of Mendelian inheritance. Trans R Soc Edinburgh. 1918;52:399–433. doi: 10.1017/S0080456800012163. DOI
Meuwissen T, Hayes B, Goddard M. Prediction of total genetic value using genome-wide dense marker maps. Genetics. 2001, 1819;157 PubMed PMC
Grattapaglia D, Resende MD. Genomic selection in forest tree breeding. Tree Genet Genomes. 2011;7:241–255. doi: 10.1007/s11295-010-0328-4. DOI
Resende MD, Resende MF, Sansaloni CP, Petroli CD, Missiaggia AA, Aguiar AM, Abad JM, Takahashi EK, Rosado AM, Faria DA, Pappas GJ, Jr, Kilian A, Grattapaglia D. Genomic selection for growth and wood quality in eucalyptus: capturing the missing heritability and accelerating breeding for complex traits in forest trees. New Phytol. 2012;194:116–128. doi: 10.1111/j.1469-8137.2011.04038.x. PubMed DOI
Resende MF, Muñoz P, Resende MD, Garrick DJ, Fernando RL, Davis JM, Jokela EJ, Martin TA, Peter GF, Kirst M. Accuracy of genomic selection methods in a standard data set of loblolly pine (Pinus taeda L.) Genetics. 2012;190:1503–1510. doi: 10.1534/genetics.111.137026. PubMed DOI PMC
Beaulieu J, Doerksen T, Clément S, Mackay J, Bousquet J. Accuracy of genomic selection models in a large population of open-pollinated families in white spruce. Heredity. 2014;113:343–352. doi: 10.1038/hdy.2014.36. PubMed DOI PMC
Beaulieu J, Doerksen TK, MacKay J, Rainville A, Bousquet J. Genomic selection accuracies within and between environments and small breeding groups in white spruce. BMC Genomics. 2014;15:1048. doi: 10.1186/1471-2164-15-1048. PubMed DOI PMC
Resende MFR, Muñoz P, Acosta JJ, Peter GF, Davis JM, Grattapaglia D, Resende MD, Kirst M. Accelerating the domestication of trees using genomic selection: accuracy of prediction models across ages and environments. New Phytol. 2012;193:617–624. doi: 10.1111/j.1469-8137.2011.03895.x. PubMed DOI
Gamal El-Dien O, Ratcliffe B, Klápště J, Chen C, Porth I, El-Kassaby YA. Prediction accuracies for growth and wood attributes of interior spruce in space using genotyping-by-sequencing. BMC Genomics. 2015;16:370. doi: 10.1186/s12864-015-1597-y. PubMed DOI PMC
Ratcliffe B, El-Dien OG, Klápště J, Porth I, Chen C, Jaquish B, El-Kassaby YA. Comparison of genomic selection models across time in interior spruce (Picea engelmannii × glauca) using unordered SNP imputation methods. Heredity. 2015;115:547–55. PubMed PMC
Bartholome J, van Heerwaarden J, Isik F, Boury C, Vidal M, Polmion C, Bouffier L. Performance of genomic prediction within and across generations in maritime pine. BMC Genomics. 2016;17:604. doi: 10.1186/s12864-016-2879-8. PubMed DOI PMC
Isik F, Bartholome J, Farjat A, Chancerel E, Raffin A, Sanchez L, Plomion C, Bouffier L. Genomic selection in maritime pine. Plant Sci. 2016;242:108–119. doi: 10.1016/j.plantsci.2015.08.006. PubMed DOI
Fuentes-Utrilla P., Goswami C., Cottrell J.E, Pong-Wong R., Law A., A’Hara S.W., Lee S.J., Woolliams J.A., QTL analysis and genomic selection using RADseq derived markers in Sitka spruce: the potential utility of within family data. Tree Genet Genomes 2017: 13: 33.
Resende RT, Resende MDV, Silva FF, Azevedo CF, Takahashi EK, Silva-Junior OB, Grattapaglia D. Assessing the expected response to genomic selection of individuals and families in Eucalyptus breeding with an additive-dominant model. SSS. 2017:1–11. PubMed PMC
Müller BSF, Neves LG, de Almeida Filho JE, Resende MFR, Jr, Muñoz PR, dos Santos PET, Filho EP, Kirst M, Grattapaglia D. Genomic prediction in contrast to a genome-wide association study in explaining heritable variation of complex growth traits in breeding populations of Eucalyptus. BMC Genomics. 2017;18:524. doi: 10.1186/s12864-017-3920-2. PubMed DOI PMC
Neves LG, Davis JM, Barbazuk WB, Kirst M. Whole-exome targeted sequencing of the uncharacterized pine genome. Plant J. 2013;75:146–156. doi: 10.1111/tpj.12193. PubMed DOI
Suren H, Hodgins KA, Yeaman S, Nurkowski KA, Smets P, Rieseberg LH, Aitken SN, Holliday JA. Exome capture from the spruce and pine giga-genomes. Mol. Ecol Res. 2016;16:1136–1146. doi: 10.1111/1755-0998.12570. PubMed DOI
Neale DB, McGuire PE, Wheeler NC, Stevens KA, Crepeau MW, Cardeno C, Zimin AV, Puiu D, Pertea GM, Sezen UU, Casola C, Koralewski TE, Paul R, Gonzalez-Ibeas D, Zaman S, Cronn R, Yandell M, Holt C, Langley CH, Yorke JA, Salzberg SL, Wegrzyn JL. The Douglas-fir genome sequence reveals specialization of the photosynthetic apparatus in Pinaceae. G3. 2017; 10.1534/g3.117.300078. PubMed PMC
Neale DB, Kremer A. Forest tree genomics: growing resources and applications. Nat Rev Genet. 2011;12:111–122. doi: 10.1038/nrg2931. PubMed DOI
Nystedt B, Street NR, Wetterbom A, Zuccolo A, Lin Y, Scofield DG, Vezzi F, Delhomme N, Giacomello S, Alexeyenko A, Vicedomini R, Sahlin K, Sherwood E, Elfstrand M, Gramzow L, Holmberg K, Hällman J, Keech O, Klasson L, Koriabine M, Kucukoglu M, Käller M, Luthman J, Lysholm F, Niittylä T, Olson Å, Rilakovic N, Ritland C, Rosselló JA, Sena J, Svensson T, Talavera-López C, Theißen G, Tuominen H, Vanneste K, Wu Z, Zhang B, Zerbe P, Arvestad L, Bhalerao R, Bohlmann J, Bousquet J, Gil RG, Hvidsten TR, de Jong P, MacKay J, Morgante M, Ritland K, Sundberg B, Lee Thompson S, Van de Peer Y, Andersson B, Nilsson O, Ingvarsson PK, Lundeberg J, Jansson S. The Norway spruce genome sequence and conifer genome evolution. Nature. 2013;497:579–584. doi: 10.1038/nature12211. PubMed DOI
Gnirke A, Melnikov A, Maguire J, Rogov P, LeProust EM, Brockman W, Fennell T, Giannoukos G, Fisher S, Russ C, Gabriel S, Jaffe DB, Lander ES, Nusbaum C. Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing. Nat Biotechnol. 2009;27:182–189. doi: 10.1038/nbt.1523. PubMed DOI PMC
Fu Y, Springer NM, Gerhardt DJ, Ying K, Yeh CT, Wu W, Swanson-Wagner R, D’Ascenzo M, Millard T, Freeberg L, Aoyama N, Kitzman J, Burgess D, Richmond T, Albert TJ, Barbazuk WB, Jeddeloh JA, Schnable PS. Repeat subtraction-mediated sequence capture from a complex genome. Plant J. 2010;62:898–909. doi: 10.1111/j.1365-313X.2010.04196.x. PubMed DOI
Walsh T, Shahin H, Elkan-Miller T, Lee MK, Thornton AM, Roeb W, Abu Rayyan A, Loulus S, Avraham KB, King MC, Kanaan M. Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82. Am J Hum Genet. 2010;87:90–94. doi: 10.1016/j.ajhg.2010.05.010. PubMed DOI PMC
Kiezun A, Garimella K, Do R, Stitziel NO, Neale BM, McLaren PJ, Gupta N, Sklar P, Sullivan PF, Moran JL, Hultman CM, Lichtenstein P, Magnusson P, Lehner T, Shugart YY, Price AL, de Bakker PIW, Purcell SM, Sunyaev SR. Exome sequencing and the genetic basis of complex traits. Nat Genet. 2012;44:623–630. doi: 10.1038/ng.2303. PubMed DOI PMC
Mertes F, El Sharawy A, Sauer S, van Helvoort JMLM, van der Zaag PJ, Franke A, Nilsson M, Lehrach H, Brookes AJ. Targeted enrichment of genomic DNA regions for next-generation sequencing. Brief Funct Genomics. 2011;10:374–86. PubMed PMC
Choi M, Scholl UI, Ji W, Liu T, Tikhonova IR, Zumbo P, Nayir A, Bakkaloğlu A, Ozen S, Sanjad S, Nelson-Williams C, Farhi A, Mane S, Lifton RP. Genetic diagnosis by whole exome capture and massively parallel DNA sequencing. Proc Natl Acad Sci U S A. 2009;106:19096–19101. doi: 10.1073/pnas.0910672106. PubMed DOI PMC
Bodi K, Perera AG, Adams PS, Bintzler D, Dewar K, Grove DS, Kieleczawa J, Lyons RH, Neubert TA, Noll AC, Singh S, Steen R, Zianni M. Comparison of commercially available target enrichment methods for next-generation sequencing. J Biomol Tech. 2013;24:73–86. PubMed PMC
Rutkoski JE, Poland J, Jannink J-L, Sorrells ME. Imputation of unordered markers and the impact on genomic selection accuracy. G3: Genes| Genomes| Genetics. 2013;3:427–439. doi: 10.1534/g3.112.005363. PubMed DOI PMC
Poland J, Endelman J, Dawson J, Rutkoski J, Wu S, Manes Y, Dreisigacker S, Crossa J, Sánchez-Villeda H, Sorrells M, Jannink J. Genomic selection in wheat breeding using genotyping-by-sequencing. Plant Genome. 2012;5:103–113. doi: 10.3835/plantgenome2012.06.0006. DOI
Ng SB, Turner EH, Robertson PD, Flygare SD, Bigham AW, Lee C, Shaffer T, Wong M, Bhattacharjee A, Eichler EE, Bamshad M, Nickerson DA, Shendure J. Targeted capture and massively parallel sequencing of 12 human exomes. Nature. 2009;461:272–276. doi: 10.1038/nature08250. PubMed DOI PMC
De La Torre AR, Birol I, Bousquet J, Ingvarsson PK, Jansson S, Jones SJM, Keeling CI, MacKay J, Nilsson O, Ritland K, Street N, Yanchuk A, Zerbe P, Bohlmann J. Insights into conifer Giga-genomes. Plant Physiol. 2014;166(4):1724–1732. doi: 10.1104/pp.114.248708. PubMed DOI PMC
Mӓrtens K, Hallin J, Warringer J, Liti G, Parts L. Predicting quantitative traits from genome and phenome with near perfect accuracy. Nat Commun. 2016;7:11512. doi: 10.1038/ncomms11512. PubMed DOI PMC
Xu S. Theoretical basis of the Beavis effect. Genetics. 2003;165:2259–68. PubMed PMC
Lande R, Thompson R. Efficiency of marker-assisted selection in the improvement of quantitative traits. Genetics. 1990;124:743–56. PubMed PMC
Whittaker JC, Thompson R, Denham MC. Marker-assisted selection using ridge regression. Genet Res. 2000;75:249–252. doi: 10.1017/S0016672399004462. PubMed DOI
Shen X, Alam M, Fikse F, Rönnegård LA. Novel generalized ridge regression method for quantitative genetics. Genetics. 2013;193:255–1268. doi: 10.1534/genetics.112.146720. PubMed DOI PMC
Gianola D, van Kaam JB. Reproducing kernel Hilbert spaces regression methods for genomic assisted prediction of quantitative traits. Genetics. 2008;178:2289–2303. doi: 10.1534/genetics.107.084285. PubMed DOI PMC
Yanchuk AD. General and specific combining ability from disconnected partial diallels of coastal Douglas-fir. Silvae Genet. 1996;45:37–45.
El-Kassaby YA, Park Y-S. Genetic variation and correlation in growth, biomass, and phenology pf Douglas-fir diallel progeny at different spacings. Silvae Genet. 1993;42:289–297.
Krakowski J, Park Y-S, El-Kassaby YA. Early testing of Douglas-fir: wood density and ring width. For Genet. 2005;12:99–105.
Beaulieu J, Doerksen T, Boyle B, Clément S, Deslauriers M, Beauseigle S, Blais S, Poulin P-L, Lenz P, Caron S, Rigault P, Bicho P, Bousquet J, Mackay J. Association genetics of wood physical traits in the conifer white spruce and relationships with gene expression. Genetics. 2011;188:197–214. doi: 10.1534/genetics.110.125781. PubMed DOI PMC
Burdon RD. Genetic correlation as a concept for studying genotype-environment interaction in forest tree breeding. Silvae Genet. 1977;26:168–175.
Owino F. Genotype x environment interaction and genotypic stability in loblolly pine. Silvae Genet. 1977;26:21–6.
Matheson AC, Raymond CA. The impact of genotype x environment interaction on Australian Pinus Radiata breeding programs. Aust. For Res. 1984;14:11–25.
Matheson AC, Cotterill PP. Utility of genotype x environment interactions. For Ecol Manag. 1990;30:159–174. doi: 10.1016/0378-1127(90)90134-W. DOI
Magnussen S, Yanchuk AD. Selection age and risk: finding the compromise. Silvae Genet. 1993;42:25–40.
Lerceteau E, Szmidt AE, Andersson B. Detection of quantitative trait loci in Pinus Sylvestris L. across years. Euphytica. 2001;121:117–122. doi: 10.1023/A:1012076825293. DOI
Ratcliffe B, Gamal el-Dien O, Klápště J, Porth I, Chen C, Jaquish B, el-Kassaby YA. A comparison of genomic selection models across time in interior spruce (Picea engelmannii x glauca) using unordered SNP imputation methods. Heredity. 2015;115:547–555. doi: 10.1038/hdy.2015.57. PubMed DOI PMC
White TL, Adams WT, Neale DB. Forest genetics. Cabi. 2007;
Neale DB, Savolainen O. Association genetics of complex traits in conifers. Trends Plant Sci. 2004;9:325–330. doi: 10.1016/j.tplants.2004.05.006. PubMed DOI
Ivanova NV, Fazekas AJ, Hebert PDN. Semi-automated, membrane-based protocol for DNA isolation from plants. Plant Mol Biol Rep. 2008;26:186–198. doi: 10.1007/s11105-008-0029-4. DOI
Howe GT, Yu J, Knaus B, Cronn R, Kolpak S, Dolan P, Lorenz WW, Dean JFDASNP. Resource for Douglas-fir: de novo transcriptome assembly and SNP detection and validation. BMC Genomics. 2013;14:137. doi: 10.1186/1471-2164-14-137. PubMed DOI PMC
Lee WP, Stromberg MP, Ward A, Stewart C, Garrison EP, Marth GTMOSAIK. A hash-based algorithm for accurate NextGeneration sequencing short-read mapping. PLoS One. 2014;9(3):e90581. doi: 10.1371/journal.pone.0090581. PubMed DOI PMC
Garrison E, Marth G. Haplotype-based variant detection from short-read sequencing. arXiv preprint arXiv:1207.3907 [q-bio.GN]. 2012;
El-Kassaby YA, Mansfield S, Isik F, Stoehr M. In situ wood quality assessment in Douglas-fir. Tree Genet Genomes. 2011;7:553–61.
Gilmour A.R., Gogel B., Cullis B., Thompson R.;ASReml user guide release 3.0. 2009
Cappa EP, Stoehr MU, Xie C-Y, Yanchuk AD. Identification and joint modeling of competition effects and environmental heterogeneity in three Douglas-fir (Pseudotsuga Menziesii Var. Menziesii) trials. Tree Genet Genomes. 2016;12:102. doi: 10.1007/s11295-016-1061-4. DOI
Garrick DJ, Taylor JF, Fernando RL. Deregressing estimated breeding values and weighting information for genomic regression analyses. Genet Sel Evol. 2009:41–55. PubMed PMC
Dutkowski GW, eSilva JC, Gilmour AR, Lopez GA. Spatial analysis methods for forest genetic trials. Can J For Res. 2002;32:2201–2214. doi: 10.1139/x02-111. DOI
Endelman JB. Ridge regression and other kernels for genomic selection with R package rrBLUP. Plant Genome. 2011;4:250–255. doi: 10.3835/plantgenome2011.08.0024. DOI
Henderson C. A simple method for computing the inverse of a numerator relationship matrix used in prediction of breeding values. Biometrics. 1976;32:69–83.
Genomic selection of juvenile height across a single-generational gap in Douglas-fir