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. 2018 Mar 9;9:306. doi: 10.3389/fpls.2018.00306

Table 1.

QTL results of DT detection via joint analysis of segregation distortion in three selected breeding populations.

QTL Chr. Bin interval Positiona (100 k) Wald valueb Donor genetic effect
Source of favorable allelec QTL/Marker previously reported
Teqing CDR22 OM1723
qDT2.8 2 915–917 312–313 10.59 -0.93 1.08 0.98 Teqing
qDT3.1 3 995–1013 0.5–15 31.85 -1.60 -1.02 -0.83 Teqing, CDR22, OM1723
qDT3.8 3 1390 311.5 10.20 -1.67 0.80 1.60 Teqing
qDT3.9 3 1447 350.5 22.96 -1.30 -0.90 -1.47 OM1723, Teqing, CDR22 QSf3, QGyp3 (Wang et al., 2013a)
qDT5.4 5 2208 247 16.72 -0.64 -1.00 1.30 CDR22, Teqing QFgwp5b, QGyp5 (Wang et al., 2014)
qDT5.5 5 2228 261 9.26 -0.54 0.94 0.90 Teqing
qDT6.3 6 2339–2347 37.5–42 11.52 -0.98 -0.06 0.25 Teqing
qDT8.4 8 3255–3257 206.5–207.5 8.75 -0.74 0.16 -0.19 Teqing QGy8 (Xu et al., 2005); QPn8, QTgw8, QSf8 (Wang et al., 2012)
qDT12.3 12 4351–4354 29–31.5 11.06 0.19 -0.85 1.17 CDR22 QPn12, QSf12 (Wang et al., 2012); QSnp12 (Wang et al., 2014)

a Position is reference to the Rice Genome Annotation Project Release 7 (RGAP 7 of Nipponbare). b P = 0.01, Wald value = 11.34; p = 0.05, Wald value = 7.81. c The genetic effects indicate that the introgression of the donors resulted in the segregation distortion loci. Indicates the significant difference at P < 0.05.