TABLE 3.
QTL associated by GWA with straighthead disease response (qStHD) in the Rice Minicore Panel (RMC) arranged in chromosomal order. Overlaps with QTL for other traits within this study, and candidate genes are also noted. Panels for which QTL are listed include “all RMC” containing all RMC accessions, indica subspecies, japonica subspecies, IND subgroup, and AUS subgroup.
| QTL | Chr | Start of QTL region (bp) a | End of QTL region (bp) a | QTL size (Mb) | Peak SNP location (bp) a | Panel the QTL peak details are from b | -log10(p) | Effect of most common allele c | Most common allele | Alternate allele | Nu. acc. with common allele | Nu. acc. with alternate allele | % Panel having alt. All RMCele | QTL overlaps among traits in this RMC study | Co-location with QTL or genes for same/similar trait reported in literature | Candidate gene RAP ID d | Candidate gene symbol(s) or name(s) e |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| qStHD1-1 | 1 | 50,85,464 | 70,49,182 | 1.964 | 57,83,885 | All RMC | 5.18 | 1.48 | T | C | 61 | 17 | 21.79 | Si, PHT | Agrama and Yan (2009) | LOC_Os01g10530 | NIP1;5 |
| ↓ | LOC_Os01g10600 | NIP1;2 | |||||||||||||||
| ↓ | LOC_Os01g11946 | ABCD1 | |||||||||||||||
| qStHD1-2 | 1 | 93,23,012 | 1,02,02,956 | 0.880 | 97,59,244 | All RMC | 5.52 | 2.26 | C | T | 60 | 15 | 20.00 | none | Agrama and Yan (2009) | LOC_Os01g18670 | ABCB1 |
| qStHD1-3 | 1 | 2,26,92,755 | 2,46,17,484 | 1.272 | 2,33,95,696 | All RMC | 5.57 | 1.75 | C | G | 67 | 11 | 14.10 | As, Si, DHD | — | LOC_Os01g41250 thru _Os01g41530 | 8 Fbox genes, Fbox021 thru Fbox028 |
| ↓ | LOC_Os01g42430 | vacuolar H + -ATPase subunit C | |||||||||||||||
| ↓ | LOC_Os01g42830 | ABCI13 | |||||||||||||||
| ↓ | LOC_Os01g42900 | ABCG2 | |||||||||||||||
| qStHD1-4 | 1 | 3,15,81,270 | 3,53,78,105 | 3.797 | 3,26,58,417 | All RMC | 5.88 | 1.98 | C | T | 60 | 12 | 16.67 | As, Si, Cu, DHD, PHT | — | LOC_Os01g55210 thru _Os01g60920 | 11 Fbox genes, Fbox038 thru Fbox048 |
| ↓ | LOC_Os01g56050 | MATE, multidrug and toxic compound extrusion | |||||||||||||||
| ↓ | LOC_Os01g58290 | Root development & fertility gene | |||||||||||||||
| qStHD2-1 | 2 | 37,23,340 | 48,46,184 | 1.123 | 37,73,340 | All RMC | 6.16 | 2.23 | G | A | 104 | 6 | 5.45 | S | — | — | — |
| qStHD2-2 | 2 | 1,85,76,987 | 2,00,69,547 | 1.493 | 1,86,26,987 | japonica | 5.98 | 2.69 | G | A | 33 | 6 | 10.81 | Si, DHD | — | — | — |
| ↓ | 1,94,06,191 | indica | 5.09 | 2.63 | G | C | 30 | 6 | 11.76 | — | — | — | |||||
| qStHD2-3 | 2 | 2,87,47,996 | 2,94,74,023 | 0.726 | 2,92,36,156 | indica | 5.96 | 2.10 | A | C | 46 | 7 | 13.21 | Si, DHD, PHT | — | LOC_Os02g45380 | MATE, multidrug and toxic compound extrusion |
| qStHD3 | 3 | 1,30,69,711 | 1,40,35,564 | 0.966 | 1,31,19,711 | All RMC | 5.39 | 1.71 | C | A | 96 | 11 | 10.28 | S | Pan et al. (2012) | — | — |
| qStHD4 | 4 | 2,21,73,581 | 2,23,30,955 | 0.157 | 2,22,23,581 | All RMC | 5.95 | 1.86 | G | T | 87 | 12 | 12.12 | DHD, PHT | — | — | — |
| qStHD5-1 | 5 | 69,56,741 | 95,87,466 | 2.631 | 93,11,338 | All RMC | 5.03 | 2.55 | C | T | 85 | 5 | 5.56 | Si, Ca | — | — | — |
| qStHD5-2 | 5 | 1,58,46,555 | 1,87,68,896 | 2.922 | 1,79,96,989 | All RMC | 5.43 | 1.53 | A | T | 83 | 15 | 15.31 | PHT | Talukdar et al. (2015) | — | — |
| qStHD5-3 | 5 | 2,72,13,787 | 2,92,55,905 | 2.042 | 2,92,05,905 | All RMC | 5.78 | 1.66 | T | A | 52 | 42 | 44.68 | Si | — | LOC_Os05g33910 | MATE2, multidrug and toxic compound extrusion protein 2 |
| qStHD6-1 | 6 | 2,12,68,226 | 2,27,22,667 | 1.454 | 2,13,32,716 | All RMC | 5.73 | 1.83 | A | T | 96 | 10 | 9.43 | Ca, PHT | — | LOC_Os06g35930 | NIP1;4 |
| ↓ | LOC_Os06g36330 | MATE, multidrug and toxic compound extrusion | |||||||||||||||
| qStHD6-2 | 6 | 2,78,50,453 | 2,80,83,810 | 0.233 | 2,79,26,998 | All RMC | 5.02 | 1.94 | A | T | 80 | 16 | 16.67 | Si | — | — | — |
| qStHD7 | 7 | 2,60,79,985 | 2,84,51,701 | 1.935 | 2,76,86,009 | All RMC | 7.8 | 1.43 | A | G | 72 | 34 | 32.08 | Si, DHD | — | — | — |
| qStHD8-1 | 8 | 4,50,806 | 28,59,799 | 2.409 | 28,09,799 | All RMC | 6.63 | 2.16 | G | T | 87 | 7 | 7.45 | As, Si, S, DHD | — | LOC_Os08g03020 | RLK1, membrane-anchored receptor-like kinase1 |
| ↓ | LOC_Os08g03380 | heat shock protein | |||||||||||||||
| ↓ | LOC_Os08g03470, 03480, 03490, 03500, 03510, 03530, 03650 | 7 BTB-domain containing genes: MB17, MB18, MBTB16 thruough MBTN19, BTBN17 | |||||||||||||||
| ↓ | LOC_Os08g05580 | NIP3;4 | |||||||||||||||
| ↓ | LOC_Os08g05590 | NIP3;2 | |||||||||||||||
| ↓ | LOC_Os08g05600 | NIP3;3 | |||||||||||||||
| qStHD8-2 | 8 | 50,81,786 | 94,26,592 | 4.345 | 60,13,173 | All RMC | 6.59 | 1.49 | C | T | 59 | 19 | 24.36 | DHD, PHT | Pan et al. (2012), Li et al. (2016), Murugaiyan et al. (2019) | LOC_Os08g10480 | ATX1; antioxidant protein1 |
| ↓ | LOC_Os08g09860 | GLO6;glycolate oxidase6 | |||||||||||||||
| ↓ | LOC_Os08g15149 | Oxidoreductase | |||||||||||||||
| ↓ | LOC_Os08g15204 | thioredoxin domain-containing protein 9 | |||||||||||||||
| ↓ | LOC_Os08g15230 | heat shock protein | |||||||||||||||
| ↓ | LOC_Os08g15330 | anthocyanidin 3-O-glucosyltransferase | |||||||||||||||
| qStHD9-1 | 9 | 15,20,138 | 51,86,402 | 3.666 | 29,93,757 | All RMC | 6.35 | 2.88 | A | G | 41 | 34 | 45.33 | As, P | — | LOC_Os09g03939 | ABCG19 |
| ↓ | LOC_Os09g06499 | SULTR4;1, sulphate transporter4;1 | |||||||||||||||
| ↓ | LOC_Os09g07450 | flavonol synthase | |||||||||||||||
| ↓ | LOC_Os09g07670 | ABC20 | |||||||||||||||
| ↓ | LOC_Os08g08920 | GLP8-1 | |||||||||||||||
| ↓ | LOC_Os08g08970 | GLP8-3 | |||||||||||||||
| ↓ | LOC_Os08g08990 | GLP8-5 | |||||||||||||||
| ↓ | LOC_Os08g09000 | GLP8-6 | |||||||||||||||
| ↓ | LOC_Os09g09930 | heavy metal transport/detoxification protein | |||||||||||||||
| qStHD9-2 | 9 | 1,01,82,415 | 1,23,66,105 | 2.184 | 1,22,98,325 | All RMC | 5.06 | -2.38 | A | C | 59 | 23 | 28.05 | none | Agrama and Yan (2009) | LOC_Os09g18390 | flavonol synthase |
| ↓ | 9 | LOC_Os09g18450 | flavonol synthase | ||||||||||||||
| ↓ | 9 | LOC_Os09g18470 | Oxidoreductase | ||||||||||||||
| ↓ | 9 | LOC_Os09g18520 | Oxidoreductase | ||||||||||||||
| ↓ | 9 | LOC_Os09g19650 | ABCA6 | ||||||||||||||
| ↓ | 9 | LOC_Os09g20000 | heavy metal-associated domain containing protein | ||||||||||||||
| ↓ | 9 | LOC_Os09g20220 | GST5, glutathione S transferase5 | ||||||||||||||
| qStHD10 | 10 | 4,19,002 | 12,79,577 | 0.861 | 11,41,117 | All RMC | 7.24 | 2.13 | G | A | 75 | 8 | 9.64 | Si, Ca, DHD, PHT | LOC_Os10g02300 | PCR1, plant cadmium resistance1 | |
| ↓ | LOC_Os10g02350 | transmembrane 9 superfamily member | |||||||||||||||
| ↓ | LOC_Os10g02750 | PAP3B;purple acid phosphatase3B | |||||||||||||||
| qStHD11-1 | 11 | 26,20,435 | 36,39,030 | 1.018 | 26,73,334 | All RMC | 5.57 | 2.64 | A | G | 86 | 6 | 6.52 | none | — | LOC_Os11g05700 | ABCC16/MRP16, multidrug resistance-associated protein16 |
| ↓ | LOC_Os11g05410 | PAP20A;purple acid phosphatase20A | |||||||||||||||
| qStHD11-2 | 11 | 2,11,29,594 | 2,29,93,035 | 1.863 | 2,29,43,035 | All RMC | 5.5 | 2.04 | G | A | 92 | 6 | 5.15 | none | Pan et al. (2012) | LOC_Os11g36430 | AIR2, arsenic induced ring protein2 |
| qStHD12 | 12 | 1,09,38,230 | 1,31,11,966 | 2.174 | 1,21,15,679 | indica | 6.86 | 3.05 | G | A | 15 | 10 | 40.00 | PHT | LOC_Os12g22110 | ABCG29 | |
| ↓ | LOC_Os12g22284 | ABCG30 |
O. sativa SNPs are identified by their physical location based on the Os-Nipponbare-Reference-IRGSP-1.0 assembly (Kawahara et al., 2013).
The panels are defined as the complete Rice Minicore Diversity Panel (RMC, n = 166). The O. sativa subpopulation groups were tropical japonica (TRJ), temperate japonica (TEJ), aus (AUS), and indica (IND). The two O. sativa subspecies are indica, composed of IND and AUS combined, and japonica comprised TEJ and TRJ. QTL were often identified in GWA-mapping of more than one population (e.g., in INDAUS and AUS). Because alternate alleles became very rare in the smaller subpopulations, the table presents the results based on the entire RMC panel when the QTL was significant there.
A negative allele effect reflects a reduction in the trait associated with the most common allele.
RAP ID is the Rice Annotation Project identification locus identified for the candidate gene.
Gene nomenclature followed the standardized nomenclature for rice genes used in Oryzabase (Yamazaki et al., 2010).