DOI: https://doi.org/10.21203/rs.3.rs-86456/v1
Rice is a semi-aquatic plant and staple food crop of more than half of the world population (Oladosu et al. 2018). It provides about 21% food need of the world and approximately 76% calorie intake of Southeast Asia (Fitzgerald et al. 2008, Miura et al. 2011). 167.25 million ha of cultivated area yielded a global production of approximately 770 million tons (FAOSTAT, 2017) with Asia producing 90%, Africa and Americas producing 4.8% and 4.6% respectively. The estimated demand because of population increase in the face of global climate change and its attendant effect on agriculture, most especially rice production has called for yield improvement of this very important cereal (Choudhury et al. 2012). Sustainable high yielding potential is often threatened by the devastating incidences of various biotic and abiotic stresses.
Rice blast is the most detrimental fungal disease among the biotic stresses that affect rice yield. Rice blast disease or rye grass blast, oval leaf spot of graminea, rice rotten neck, Johnson’s spot, pitting disease, rice seedling blight, rice blast fungus and blast of rice, are caused by Magnaporthe oryzae. This disease has been reported in over 85 rice growing countries (Wang et al., 2014), which has led to 70 to 80% yield losses depending on the severity (Miah et al. 2017). Due to this disease, economic losses of over $70 billion of abundant rice to feed more than 60 million were reported due to blast (Miah et al. 2017). Bacterial leaf blight is another potential threat to rice cultivation which was reported to have decimated yield up to 50% depending on incidence level (Scardaci et al. 2003). Drought is a threat to rice production in Asia and Africa, with reported effect on 23 million hectares (Kumbhar et al. 2015; Bray et al. 2000) with yield losses of up 100% depending on duration and time water deficit.
Putra-1 rice variety is a product of a high yielding MR219 blast susceptible rice cultivar and Pongsu Seribu 1, a blast resistance cultivar with poor yield. It has a broad-spectrum blast resistance with Piz, Pi2 and Pi9 genes (Miah et al. 2016). Similarly, drought tolerant MR219-PL-137 rice variety was developed by pyramiding of three drought yield quantitative trait loci (QTLs); qDTY2.2, qDTY3.2, qDTY12.1 from IR77298-14-1-2-10 (IR64 + Aday Sel), IR8196-B-B-195 (Swarna + Apo), IR84984-83-15-18-B (Vandana + Way Rarem) respectively, with consistent effect on grain yield during reproductive-stage drought stress, it was developed through marker-assisted breeding (Shamsudin et al. 2016). Also, IRBB60 has high resistance with disease rating of one and 0.5 cm lesion length. It is a product of pyramiding of IR24 with IRBB4, IRBB5, IRBB13 and IRBB21 Xa4 + xa5 + xa13 + Xa21, it crossed and produced IRBB50 (Xa4 + xa5), IRBB52 (Xa4 + Xa21) and IRBB53 (xa5 + Xa21) thereby producing a variety IRBB60 with Xa4 + xa5 + xa13 + Xa21 (Habarurema et al. 2013; Huang et al. 1997). The variety is a broad-spectrum bacterial leaf blight resistance variety with four R genes Xa4, xa5, xa13 & Xa21 (Baliyan et al. 2016).
Shamsudin et al. (2016) reported that marker-assisted pyramiding allows breeders to introgress two or more genes of biotic and or abiotic stresses into a single variety of plant. This will enable the plant to maintain its yield in the face of single or multiple and simultaneous infection/stress of disease pathogens/drought stress due to host resistance and tolerance to biotic and abiotic stresses respectively. Therefore, the objectives of these research were to identify the polymorphic markers at the target region (parental survey) and screened for selection of variety with multiple traits of resistance to blast, bacterial leaf blight and drought tolerance by genotyping and phenotyping.
Plant Materials and Breeding Design
Two high yielding rice; Putra-1 (blast resistance), MR219-PL-137 (Drought tolerant) and IRBB60 (Bacterial leaf blight resistant) varieties were crossed by pedigree breeding method in a single, three-way (and reciprocal) and double crosses breeding scheme to produce single line with multiple traits through pyramiding approach by using marker-assisted selection. The experiment was conducted in a glass house at the Rice Research Centre (RRC) and Laboratory of Climate and Smart-Food Crop Production, Universiti Putra Malaysia (UPM).
Breeding Scheme to Develop Hybrid Disease Resistance and Tolerance Lines
The procedures used to develop improved lines with multiple traits of blast resistance, bacterial leaf blight and drought tolerance are shown in Figure 1.
Genomic DNA Extraction
Complete genomic DNA of each of the plant samples collected was extracted from the leaf tissues of 2-4 weeks old of the parental cultivars and progenies of individual plants using Cetyltrimethylammonium bromide (CTAB) method protocol Doyle and Doyle (1987) with modification following the protocol of McCouch et al. (1988).
The DNA pellet (crude form) was washed with 75% ethanol and dissolved in 50µl TE buffer and then treated with RNAse. The quality and integrity of the DNA were quantified using Nanodrop spectrophotometer (ND1000 Spectrophotometer) to determine the concentration and purity of samples.
Molecular markers
Some primers polymorphic to the different genes responsible for blast resistance, bacterial leaf blight and drought tolerance were selected through the gramene data base. Linked markers associated with the genes of interest were selected from published article for foreground selection which included; Blast resistance (Ashkani et al. (2011), Pinta et al. (2013), Miah et al. (2016), drought tolerance (Shamsudin et al. 2016). Some of the primers were mapped by Miah et al. (2016), for blast resistance, (Miah et al. 2016) and (Shamsudin et al. 2016) for drought tolerance, and bacterial leaf blight (Pinta et al. 2013; He et al. 2006; Khan et al. 2015; Pradhan et al. 2015)as indicated in Table 1.
Amplification and electrophoresis
Primer pairs were optimized for polymerase chain reaction (PCR) to amplify microsatellite loci. Parental survey of the three varieties was carried out to identify polymorphic SSR markers among the parental varieties. The total PCR reaction of 15μL contained 70ng template DNA, 1.0 μmol L−1 concentration of each primer, 7.5μL master mix (Thermo Scientific, Waltham, MA, USA) and 4.5μL nuclease-free water. PCR amplification was carried out in a thermocycler (T100TM, Bio-Rad, Hercules, CA, USA) following the initial denaturation at 940C for 5 min followed by 35 cycles at 940C for 30 s, 550C for 30 s, 720C for 30 s and a final extension at 720C for 5 min, followed by rapid cooling to 40C prior to analysis for conventional protocol while the touch procedure used was; the lid temperature was 1050C, denaturation, annealing and elongation temperatures as follows; (1. 940C for 3mims, (2. 940C for 30sec, (3. 620C for 1min., +10C per cycle (4. 720C for 30sec., (5. Go to step 2, 9× (6. 940C, 30sec. (7. 520C, 1min., (8. 720C, 2mins., (9. Go to step 6, 29×., (10. 720C, 10mins. (11. rapid cooling to 40Cꝏ, and (12. 120C ꝏprior to analysis.
Gel electrophoresis was carried out where 5μL of PCR product was mixed with loading dye (ladder) and run using 2.0% MetaphorTM agarose (Lonza) gel containing 5-10𝜇L Midori green in 1× TBE buffer (0.05 mol L−1 Tris, 0.05 mol L−1 boric acid, 1 mmolL−1 EDTA, pH 8.0). The gel was run at a constant voltage of 80V for 60 minutes. Band pattern was documented under UV light and analyzed using Molecular imager system (GelDocTM XR, BioRad) for amplified products.
Identification of polymorphic and linked markers for parental survey and selection of improved lines using gel electrophoresis
Two paired parents of donors and recurrent (recipients) used to determine polymorphisms are Putra-1(Blast)×MR219-PL-137 (drought tolerance), Putra-1(Blast) × IRBB60 (BLB).
Biparental cultivars with MR219-PL-137 and IRBB60 designated as donors were dusted on Putra-1 used as recipient parent each for the donor parent cultivars. The markers identified during parental survey are RM6836, RM8225 for blast resistance (Putra-1) which served as polymorphic and linked markers. RM236, RM520, RM511, RM1261 comprised of polymorphic, linked and flanking markers for drought tolerance in MR219-PL-137 line, while IRBB60 had markers RG136, Xa13Prom, RM224, RM122, RM21, pTA248 as both polymorphic and linked to genes of resistance as shown in Table 1.
Table 1. Polymorphic and linked microsatellite (SSR) markers used for parental survey and associated to genes of resistance and quantitative trait loci (QTL)/Flanking markers
Variety |
Genes |
Primer sequences (5′ –3′) |
Chr. position |
Exp. size |
References |
|
SSR linked marker |
Forward primer |
Reverse primer |
||||
Putra-1(Blast resistance) |
||||||
RM6836 |
Piz, Pi2, Pi9 |
TGTTGCATATGGTGCTATTTGA |
GATACGGCTTCTAGGCCAAA |
6 |
240 |
(Miah et al., 2016; Akos et al., 2019ab) |
M8225 |
Piz |
ATGCGTGTTCAGAAATTAGG |
TGTTGTATACCTCATCGACAG |
6 |
221 |
(Miah et al., 2016) |
MR219-PL-137 drought tolerance |
||||||
RM511 |
qDTY12.1 |
CTTCGATCCGGTGACGAC |
AACGAAAGCGAAGCTGTCTC |
12 |
130 |
(Shamsudin et al., 2016) (Shamsudin et al., 2016) (Shamsudin et al., 2016) (Akos et al., 2019b) (Mishra et al., 2013) (Bernier et al., 2007) |
RM520 |
qDTY3.1 |
AGGAGCAAGAAAAGTTCCCC |
GCCAATGTGTGACGCAATAG |
3 |
247 |
|
RM236 |
qDTY2.2 |
GCGCTGGTGGAAAATGAG |
GGCATCCCTCTTTGATTCCTC |
2 |
174 |
|
RM276 |
qDTY2.2,3.1 |
CTCAACGTTGACACCTCGTG |
TCCTCCATCGAGCAGTATCA |
6 |
149 |
|
RM1261 |
qDTY12.1 |
GTCCATGCCCAAGACACAAC |
GTTACATCATGGGTGACCCC |
12 |
167 |
|
IRBB60 (Bact. leaf blight) |
||||||
RM224 |
Xa-4 |
ATCGATCGATCTTCACGAGG |
TGCTATAAAAGGCATTCGGG |
11 |
157 |
(He et al., 2006) (Wu and Tanksley, 1993) (Khan et al., 2015) |
RM122 |
xa-5 |
GAGTCGATGTAATGTCATCAGTGC |
GAAGGAGGTATCGCTTTGTTGGAC |
5 |
227 |
|
RM13 |
xa-5 |
TCCAACATGGCAAGAGAGAG |
GGTGGCATTCGATTCCAG |
5 |
141 |
|
RG136 |
xa-13 |
TCTTGCCCGTCACTGCAGATATCC |
GCAGCCCTAATGCTACAATTCTTC |
8 |
246 |
(Zhang et al., 1996) (Akos et al., 2019bc) (Chen et al., 1997) (Ronald et al., 1992) |
Xa13Prom |
xa13 |
GCCATGGCTCAGTGTTTAT |
GAGCTCCAGCTCTCCAAATG |
8 |
- |
|
RM21 |
Xa-21 |
ACAGTATTCCGTAGGCACGG |
GCTCCATGAGGGTGGTAGAG |
11 |
157 |
|
pTA248 |
Xa-21 |
AGACGCGGAAGGGTGGTTCCCGGA |
AGACGCGGTAATCGAAGATGAAA |
11 |
- |
Note: Chr. (Chromosome) position, Exp. (Expected) base pair size
Bacterial and Fungal Culture
Bacterial leaf blight (Xanthomonas oryzae pv oryzae) MXO 1552 and blast (Magnaporthe grisea) fungus with virulent pathotype P7.2 were obtained from the Malaysia Agricultural Research and Development Institute (MARDI), Serdang and sub-cultured in nutrient agar (NA) and potato dextrose agar (PDA) respectively for use. The former was incubated at 300C for 48hours (Suresh et al. 2013), while the latter was incubated at 250C for 14 days (Mahdieh et al. 2013).
Diseases inoculation, tolerance imposition and evaluation
M. grisea the most virulent pathotype P7.2 and X. oryzae MX0 1552 were used to screen susceptible and improved lines for resistance to blast and bacterial leaf blight pathogens. Drought tolerance was also screen at an in vivo condition at RRC, UPM by subjecting the plants at reproductive stage to drought stress condition. Young seedlings of 2-3 weeks were inoculated with suspension of blast 1.9×105 conidia mL-1 in a high relative humidity (>90%) for 48hrs, and then observed after 7 days for disease infection. Blast lesion degree was scored and evaluated according to (IRRI-SES 2014) glass house scale of 0-9. The plants lesion scores are thus; 0-2, were considered as resistant (R), score of 3 considered as moderately resistant (MR) and scores of 4-6 as MS, while 7-9 as S.
The suspension of bacterial leaf blight (X. oryzae) pathogen at concentration of 109 cells/ml from 48hrs cultured Xoo bacterium (Banito et al., 2012). Young seedlings of 3-4weeks old were clip inoculated on leaves 1-2cm from the tip of leaves. Plants lesion lengths were measured after 14 days using meter rule in centimetres and scored according to IRRI-SES, (2014). Banito et al. (2012) glasshouse scale and modification according to Amante-Bordeos et al. (1992) 0-5 considered as R, >5-10 as MR, >10-15 as MS, while >15 were considered as S.
Drought stress condition was imposed to test for drought tolerance according to IRRI-SES scale with slight modification at reproductive stage, which is between 70-90 days after sowing and it is considered as the most sensitive stage of rice growth. One week of severe drought is capable of greatly affecting rice under glass house experiment (IRRI-SES, 2014).
Marker assisted selection
Parental survey was carried out to identified markers polymorphic to blast resistance genes (RM6836, RM8225), bacterial leaf blight (Xa13Prom, pTA248, RM164 ) and drought tolerance (RM520, RM511, RM1261), these markers are also linked to the genes/QTLs of interest and were similarly used on the same traits by Ashkani et al. (2011); Pinta et al. (2013); Miah et al. (2016); Khan et al. (2015); Shamsudin et al. (2016). In F1 generation, crosses between Putra-1 (blast resistance) and MR219-PL-137 drought tolerance cultivars and between Putra-1 and IRBB60 (bacterial leaf blight) was carried out, true F1 were those plants with heterozygous amplification. The two F1s crossed together generated a double-crossed population. While each F1 was crossed with one of the varieties lacking in its F1 which produced three-way crosses, the initial F1s were maintained as single crosses. In F2 segregating generation, the homozygous resistant plants similar to recipient parent (banding pattern alignment) were selected using the polymorphic and linked markers (RM6836, RM8225) and (RM520, RM511 and RM1261) for three-way cross and reciprocal with MR219-PL-137 drought tolerant line as the recipient parent, and the heterozygous and homozygous similar to the two parents and donor respectively were not selected as was represented in similar fashion as the Mendelian ratio 1:2:1 (Figures 2-12).
Genotyping selection in segregation lines (F2) for target genes using gel electrophoresis for single, double and three-way crosses
The Mendelian segregation generation is often an F2 generation represented by ratio 1:2:1 shown in the banding pattern by gel electrophoresis. The parental bands were standard band to gauge the orientation of the progeny bands, these were arranged in the order of cross pollination with the recipient often the first, followed by the donor either in single, double or three-way cross. Each of the aligned band tallied with recipient parent as single band (ratio 1), heterozygote, the two parents of recipient and donor (ratio 2) and donor parent as the last band of 1 in the ratio. The polymorphic markers created this pattern of selection, but the selection at this segregating generation was basically for the band aligning with the recipient parent (Mishra et al. 2013; Chen et al. 1997) (Figures 13-16)
Pure-line selection of F4 single, F3 three-way and F3(2) double crosses using
Non-segregating F4 single crosses, F3 three-way, and F3(2) double crosses lines were selected F2 recipient lines in a segregating generation that self-pollinated resulting in improved stable lines that corresponded to the recipient parent which is Putra-1 (blast resistance), except for the reciprocal cross where the recipient parent was MR219-PL-137 drought tolerance variety. Polymorphic markers were used to determine plants selected (Mishra et al. 2013; Chen et al. 1997) (Figures 17-21).
Phenotyping
This is a strategy used in selection of rice plants that have shown resistance and tolerance to pathogens and water stress situations respectively. It is also a process known as “challenging”, the rice plants (progenies) introgressed with desired traits of resistance and tolerance QTLs determined by linked markers to the traits were infected with pathogens whose resistance and tolerance were introgressed. This basically revealed the levels of expression of resistances and tolerance of genes/QTLs introgressed, it is similar to gene expression determine through western blot analysis. The procedures were according to IRRI-SES (2014) with slight modifications.
Infested glasshouse and selection of F1
The F1 rice plants were grown in a highly blast infested environment without prior treatment with fungicide, so that it can challenge the plants and those that survived were selected and advanced to the next generation of self pollination, double and three-way crosses. This exposed the plant to varied strains of the pathogens within the environment and selection was carried out (Figure 22 g & h). The inability to resist blast even though as hybrid was because it was not a stable line which implied that it was not yet integrated in the plant and could not be expressed.
Selection of resistance and tolerance lines
The success of this selection entailed that the genes/QTLs introgressed to produce the improved lines were expressed, and the resultant effect is that when the pathogens and water deficit conditions were appropriately introduced to the plants, they showed resistance and tolerance, except on the susceptible (Control) parent plants, which actually showed susceptibility as shown in Figure 22(c,d,g,h). The blast’s three R genes conferred resistance to leaves at all stages of growth, likewise bacterial leaf blight with four R genes, and also drought tolerance with three qDTY. The potential of developing resistance to blast and bacterial leaf blight are possibilities attainable, the Figure 23 showed the scores of both traits inoculated with the disease pathogens, it recorded resistant (R) and moderately resistant (MR) to blast and bacterial leaf blight for M. grisea and X. oryzae respectively. These results agreed with the findings of Chen et al. 1997 and Miah et al. 2017 on the development of blast resistant variety. Sun et al. (2004) and Zhang et al. (2009) reported that Xa21 gene was the best to induced resistance against BLB. These R genes were also introgressed in the improved lines.
Table 2 Genotypic and phenotypic segregation of resistance (R.) heterozygous (H) and susceptible (S) to rice in parental, F1 hybrid and F2 populations
Population |
Expected ratio |
Observed frequency |
Chi-square |
P-value |
||
R:H:S |
R |
H |
S |
|||
F2 (PD) |
||||||
PR |
6 |
- |
- |
|||
PS |
- |
4 |
||||
F1 hybrid |
- |
11 |
- |
|||
F2 genotype |
1:2:1 |
18.5 |
5.99 |
|||
F2 Phenotype |
3:1 |
16 |
- |
4 |
3.58 |
3.84 |
F2 (PB) |
||||||
PR |
2 |
- |
- |
|||
PS |
- |
- |
9 |
|||
F1 hybrid |
- |
1 |
- |
|||
F2 genotype |
1:2:1 |
149.69 |
5.99 |
|||
F2 Phenotype |
3:1 |
3 |
- |
9 |
20.5 |
3.84 |
F2 (PBD) |
||||||
PR |
3 |
- |
- |
|||
PS |
- |
- |
2 |
|||
F1 hybrid |
- |
12 |
- |
|||
F2 genotype |
1:2:1 |
13.5 |
5.99 |
|||
F2 Phenotype |
3:1 |
15 |
- |
2 |
5.75 |
3.84 |
F2 (PDB) |
||||||
PR |
6 |
- |
- |
|||
PS |
- |
- |
4 |
|||
F1 hybrid |
- |
11 |
- |
|||
F2 genotype |
1:2:1 |
28 |
5.99 |
|||
F2 Phenotype |
3:1 |
17 |
- |
4 |
10.42 |
3.84 |
F2 (DPB) |
||||||
PR |
5 |
- |
- |
|||
PS |
- |
- |
7 |
|||
F1 hybrid |
- |
8 |
- |
|||
F2 genotype |
1:2:1 |
31 |
5.99 |
|||
F2 Phenotype |
3:1 |
13 |
- |
7 |
16.83 |
3.84 |
Phenotype df(2) @ 0.05; Genotype df(1) @ 0.05
Selection for inheritance of resistance and tolerance
Total of 20 heterozygous F1 plants selected were advanced to the next generation by selfing (F2), double cross (F1(2)) and three-way crosses (F1). A total of 102 F2, single cross, F1(2) double and F1 three-way crosses were evaluated for genotyping analysis using polymorphic and linked markers as presented in Table 2. The F2 was segregated as resistance (aligning with the recipient female), susceptible (donor male) and heterozygous scored markers. While F1(2) was selected based on resemblance to parents (recipient female of initial F1 and new donor for the three-way cross and double cross) as F1 heterozygous. The F1(2) is similar to F1 and therefore only the heterozygous plants were selected.
There was an interplay of genes of inheritance among blast M. grisea, BLB X. oryzae and Drought MR219-PL-137 (drought tolerance) in the F2 single, double and three-way crosses. All the traits for resistance and tolerance had dominant and recessive genes as shown in Table 2 The statistical value in the populations PD (Putra-1 and MR219-PL-137 drought tolerance) single cross F2 phenotype was less than the P-value. The phenotypic t calculated and t tabulated values are 3.58 and 3.84 respectively. Therefore, there is no significant difference P≤0.05 and so, does not conform to 3:1 Mendelian ratio. The genotypic t calculated and t tabulated values of the chi-square are 18.5 and 5.99 respectively. Therefore, it is significant (P≤0.05), which conformed to the Mendelian genotypic ratio (1:2:1). This non conformity of phenotypic ratio 3:1 could be attributed to epistasis and linkage effect. However, considering PB (Putra-1 and IRBB60), PBD, PDB and DPB populations, the genotypic and phenotypic ratio conformed to Mendelian chi-square statistics (P≤0.05) in the F2 generation. The t calculated were greater than t tabulated. It corroborated with the findings of 18, although on single gene model. This research introgressed multiple genes, but dominance-recessive effect conformed to the model as well as the single gene model. This was also visible in the F4 single, F3(2) double and F3 three-way crosses stable non-segregating pure-lines generation. This principle was always applied in all breeding research which often result to multiplication of seeds and released as new variety after multi-locational evaluation (Nyguist and Baker, 1991; Acquaah, 2007).
Means comparison of days to 50% flowering (DTF) showed that the susceptible variety (CONTROL) recorded more days compared to other improved lines when imposed with reproductive stage drought stress. The susceptible (Control) took an average of between 95-98days to 50% flowering, while the improved lines had the lowest and maximum days of 92-95 days. The stress was imposed for >2weeks starting from intermediate to severe stress with leaves turned from U-shaped to 0-shaped respectively. Over ten days of severe drought stress imposed against the seven days of reproductive drought stress recommended for glass house (IRRI-SES, 2014). Other parameters observed included; panicle length (PL), fully filled grain and (FFG), yield maturity (YM). These traits are reproductive stage influenced and therefore, their responses to effect of drought was important in determining their level of tolerance (Figure 24).
The average panicle length for control (susceptible) and improved lines under reproductive stage drought stress was 20cm and 24cm respectively, while the fully filled grain (FFG) was similarly 27g and 44g, and yield maturity was 132 days and 128 days respectively. Water deficit stress delays flowering and more so when the cultivar has no tolerant QTLs. It was recorded that although both were subjected to the same stress condition, the improved lines with QTLs flowered somewhat earlier. This corroborated with the reports and findings of Pantuwan et al. (2002); Lanceras et al. (2004); Atlinet al. (2006); Jongdee et al. (2006); Ouk et al. (2006); Venuprasad et al. (2007); Zhao et al. (2010); Blum (2011); Vikram et al. (2011); Ghimire et al. (2012) that reproductive stage drought stress delays flowering. The percentage of FFG yield of 27g and 44g was 15.13% and 24.66% for susceptible and improved lines respectively. According to Yambao and Ingram (1988) yield reduction of up to 70%, 88% and 52% when rice was imposed drought stress for 15 days at panicle initiation stage, flowering and grain filling stage respectively was considered tolerant (Kano-Nakata et al. 2014). however stated that any drought protocol that has the potential of reducing yield to 65% compared to those under no drought stress could be considered as drought tolerant. This conveniently agrees with our result of 75% reduction.
Delay in flowering would normally result in delay in yield maturity because a stage was delayed. The physiological and biochemical processes adjusted in response of stress to conserve water as a system of adaptation, it slowed down the processes thereby causing delay. This emphasizes the importance of water to plants (Juraimi et al. 2009). The reproductive stage drought stress was delayed to 133days to attend physiological maturity with the susceptible line, while the improved tolerant line was 128 days. A check on the drought tolerant variety under non stress condition matured at an average of 118 days.
Report shows that qDTY12.1 and qDTY3.1 conferred tolerance and produce high yield with increasing drought effect in upland (Wu and Tanksley, 1993), and in lowland (Venuprasad et al. 2009) respectively. Zhang et al. (1996) reported qDTY12.1 as the first QTL with large effect of grain yield on reproductive stage drought stress. Similarly, QTLs qDTY12.1and qDTY3.2with confirmed large effects also recorded in Nepal (Bernier et al. 2007; Yadaw et al. 2013). Figure 25 and Figure 26 shows the stages and pattern of rice growth under normal stress-free and in reproductive stage drought stress conditions, from planting to when drought stress was imposed (reproductive stage), and when the plants flowered (heading) to yield maturity in each of the 4 populations of the improved lines which had drought tolerance QTLs introgressed based on parental traits crossed.
Improved lines of high yielding and diseases resistance and drought tolerance rice were developed from three parents. These were properly selected based on the genotyping results obtained through gel electrophoresis and with the aid of the polymorphic markers which formed the bases for accurate gene introgression and selection. The polymorphic and linked markers to the R genes of the disease pathogens (Blast, Bacterial leaf blight) and the drought tolerant QTLs were used and confirmed to be present on the selected segregating generations to non-segregating, pure-line selection, either as single (F4), double (F3(2)) and three-way (F3) crosses. The susceptible varieties confirmed the level of resistance of the improved lines. The reproductive stage drought test showed that the yield was within acceptable range for drought tolerant varieties. These lines are therefore, suitable for cultivation in lowlands and low water availability to mitigate the effect of climate change.
Description of letter symbol used
Characteristics |
Denotation |
Description |
PB PD PBD PDB DPB Population Resistant Moderately resistant Moderately susceptible Susceptible Potato dextrose agar Nutrient agar |
F1(PB) F1(PD) PBD PDB DPB Pop. R MR MS S PDA NA |
Cross between Putra-1 and IRBB60 Cross between Putra-1 and MR219-PL-137 3-way cross between putar1 and IRBB60(F1) and MR219 Drought tolerant Double cross (from two F1s; P×D and P×B) 4-way reciprocal cross (between MR219-PL-137 drought tolerant and F1 Putra-1×IRBB60) Population signifies the breeding or crossed lines Score of measure of resistance to pathogens Score of moderate resistance Measures and score for moderately susceptible to pathogen Measure of plants susceptibility to pathogens Growth media for fungi Media for growing bacteria |
Ethical Approval and Consent to participate
Not applicable
Consent for publication
Not applicable
Availability of data and materials
Not applicable for all, but for those applicable are available on demand
Competing interests
Authors declare that they have no competing interests
Funding
Not applicable
Authors’ contributions
MYR conceived the study and was also involved in the design and project coordination. ISA drafted the manuscript and laboratory experiment. MRI, SIR, NAAS and ABR also participated in the breeding design, protocols for phenotyping and molecular (genotyping) experiment and project coordination. OY and IM involved in the analysis and formatting.
Acknowledgments
The authors express gratitude to the Heads, Laboratory of Climate-Smart Food Crop Production, Institute of Tropical Agriculture and Food Security, and Rice Research Centre (RRC), Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia.
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