QTL mapping in autotetraploids using SNP dosage information.
QTL mapping in autotetraploids using SNP dosage information.
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DOI:
10.1007/s00122-014-2347-2
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发表时间:
2014-09
影响因子:
5.4
通讯作者:
Bryan, Glenn J.
中科院分区:
文献类型:
--
作者:
Hackett, Christine A.;Bradshaw, John E.;Bryan, Glenn J.
Dense linkage maps derived by analysing SNP dosage in autotetraploids provide detailed information about the location of, and genetic model at, quantitative trait loci. Recent developments in sequencing and genotyping technologies enable researchers to generate high-density single nucleotide polymorphism (SNP) genotype data for mapping studies. For polyploid species, the SNP genotypes are informative about allele dosage, and Hackett et al. (PLoS ONE 8:e63939,) presented theory about how dosage information can be used in linkage map construction and quantitative trait locus (QTL) mapping for an F1 population in an autotetraploid species. Here, QTL mapping using dosage information is explored for simulated phenotypic traits of moderate heritability and possibly non-additive effects. Different mapping strategies are compared, looking at additive and more complicated models, and model fitting as a single step or by iteratively re-weighted modelling. We recommend fitting an additive model without iterative re-weighting, and then exploring non-additive models for the genotype means estimated at the most likely position. We apply this strategy to re-analyse traits of high heritability from a potato population of 190 F1 individuals: flower colour, maturity, height and resistance to late blight (Phytophthora infestans (Mont.) de Bary) and potato cyst nematode (Globodera pallida), using a map of 3839 SNPs. The approximate confidence intervals for QTL locations have been improved by the detailed linkage map, and more information about the genetic model at each QTL has been revealed. For several of the reported QTLs, candidate SNPs can be identified, and used to propose candidate trait genes. We conclude that the high marker density is informative about the genetic model at loci of large effects, but that larger populations are needed to detect smaller QTLs. The online version of this article (doi:10.1007/s00122-014-2347-2) contains supplementary material, which is available to authorized users.
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影响因子:
3.7
作者:
Baird NA;Etter PD;Atwood TS;Currey MC;Shiver AL;Lewis ZA;Selker EU;Cresko WA;Johnson EA
通讯作者:
Johnson EA
DOI:
10.1007/s004380050800
发表时间:
1998-08-01
期刊:
MOLECULAR AND GENERAL GENETICS
影响因子:
--
作者:
Meyer, RC;Milbourne, D;Waugh, R
通讯作者:
Waugh, R
影响因子:
64.8
作者:
Kloosterman, Bjorn;Abelenda, Jose A.;Bachem, Christian W. B.
通讯作者:
Bachem, Christian W. B.
影响因子:
1.9
作者:
MacKenzie, Katrin;Hackett, Christine A.
通讯作者:
Hackett, Christine A.
影响因子:
3.7
作者:
Elshire RJ;Glaubitz JC;Sun Q;Poland JA;Kawamoto K;Buckler ES;Mitchell SE
通讯作者:
Mitchell SE