Table 1.
Trait | Na | Thresh.b | ICMc | cMd | LODe | Expl. Varf | Modelg | Act.h | Dir.i | Effectj | SEk |
---|---|---|---|---|---|---|---|---|---|---|---|
Stem length | 121 | 4.0 | 2 | 19 (19.8)l | 4.4 (4.6)l | 0.14 (0.15)l | oQ2Q3o × ooQ7Q8 | CD | — | **** | **** |
Stem prickles | 121 | 4.4 | 3 | 22 (27.4) | 6.5 (7.8) | 0.21 (0.25) | ooQQ × Qooo | SD | + | 2.75 | 0.67 |
4 | 74 (74.5) | 5.8 (6.1) | 0.19 (0.20) | oooQ × oQoo | A | − | 1.92 | 0.34 | |||
6 | 14 (14.4) | 4.4 (4.1) | 0.14 (0.13) | QQoQ × oQoo | A | − | 1.61 | 0.32 | |||
Petiole prickles | 121 | 4.5 | 4 | 66 (64.7) | 6.7 (7.0) | 0.21 (0.22) | QQoo × Qooo | A | + | 0.78 | 0.12 |
Num. petals | 120 | 5.2 | 2 | 88 (92.7) | 6.5 (7.1) | 0.21 (0.23) | QooQ × oooQ | A | + | 8.62 | 1.46 |
3 | 27 (33.7) | 6.1 (6.6) | 0.20 (0.21) | oQQo × oooQ | DD | − | 6.71 | 1.01 | |||
Chlorophyll | 121 | 3.0 | 4 | 50 (50.3) | 3.3 (3.5) | 0.11 (0.11) | oQQo × QQoo | SD | + | 2.95 | 0.95 |
aN number of offspring for which genotype and phenotype data were available for each trait
bThresh. experiment-wide LOD significance threshold, determined by permutation test with N = 1000 and α = 0.05
cICM chromosomal linkage group, using the integrated consensus map (ICM) numbering of Spiller et al. (2011) and Bourke et al. (2017)
dcM centiMorgan position of QTL peak
eLOD logarithm of odds at QTL peak
fExpl. Var. fraction of phenotypic variance explained by the QTL model at the peak position ( of the linear model)
gModel QTL model that best fit the data at the QTL position (i.e. minimised the BIC). “Q” signifies a predicted QTL allele with an estimated effect, whereas “o” denotes an allele with neutral effect (i.e. the remaining, grouped alleles at a QTL whose effects are not estimated). In cases where the most likely model was multi-allelic, subscripts (Q1 etc.) are used to denote the parental origin of the allele. Note that in the case of dominance, the Q (or QQ) alleles are taken to be dominant
hAct. mode of action of QTL model, A (bi-allelic) additive, CD (multi-allelic) codominant, SD (bi-allelic) simplex dominant, DD (bi-allelic) duplex dominant
iDir. Direction of the allele effect, either positive (+), i.e. increasing trait value, or negative (−). In the case of multiple QTL alleles, the direction of each QTL allele Qn is given
jEffect QTL allele effect, estimated using the slope of a (weighted) regression of the genotype means from the 36 genotype classes against the QTL allele count (coded as 0/1 in the case of both simplex or duplex dominance to signify the absence or presence of the dominance-causing alleles)
kSE standard error of the estimated slope of the regression line
lNumbers shown are results from initial QTL scan, with those in parentheses the results following re-saturation of QTL region with additional markers
****Q2 = 1.28 ± 1.76, Q3 = 2.35 ± 1.73, Q7 = 2.78 ± 1.73, Q8 = 5.87 ± 1.47