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Rice blast is arguably the most devastating fungal disease of rice. Utilization of resistance genes to breed resistant cultivars is one of the most economical and environmentally friendly approaches to combat the disease. Pi25, a major resistance gene conferring broad-spectrum resistance to both leaf and neck blast, is an ideal gene resource to improve the resistance of rice varieties to blast. Recently, several allele-specific markers were developed. However, they were deficiently efficient due to either an additional process of restriction enzyme digestion for cleaved amplified polymorphic sequence (CAPS) markers or the risk of false-positive error in identifying susceptible Tetep allele (Pi25TTP) for PCR-based markers. In this study, based on a conserved single nucleotide polymorphism (SNP) between resistant and susceptible alleles, a tetra-primer amplification refractory mutation system (ARMS)-PCR marker was developed. The new marker, namely Pi25-2687R3, could effectively distinguish the resistant Gumei 2 (GM2) allele (Pi25GM2) and the susceptible allele Pi25TTP. Moreover, a perfect consistency of genotyping was exhibited between Pi25-2687R3 and published CAPS marker CAP3/Hpy 99I. A more accurate genotyping was also displayed compared to the previous PCR-based SNP marker Pi25-2566. Our finding proved that Pi25-2687R3 could achieve the same result as CAP3/Hpy 99I with less workload and cost and could promote the accuracy in the identification of genotypes superior to Pi25-2566. This study provided a quick and reliable functional marker for discriminating Pi25 alleles, which would be a valuable tool for genotypic assay and rice molecular breeding of blast resistance. [ABSTRACT FROM AUTHOR]

Rice is sensitive to high-temperature stress during almost all stages of growth and development. High-temperature stress has become one of the main factors restricting high yield and superior quality of rice. In this study, recombinant inbred lines (RILs) derived from an indica rice cross between two restorer lines were planted in two years. One sowing date was applied in 2019, and four sowing dates were set in 2020 according to the period of local high temperatures in recent years. Two traits closely related to high-temperature tolerance, heading date (HD), and spikelet fertility (SF) were measured. In each trial, the HD showed a bimodal distribution, whereas SF had a continuous and left-skewed distribution. QTL analysis was performed using a high-density bin map. For HD, a total of six QTL were detected. All of them correspond in position to the cloned genes, among which qHD8 in the DTH8/Ghd8 region showed the largest genetic effect. For SF, a total of eight QTL were detected. Five of them, qSF1, qSF2, qSF3.1, qSF3.2, and qSF8, showed high-temperature tolerance and had an important potential in rice breeding. [ABSTRACT FROM AUTHOR]

Grains number is one of the most important agronomic traits in the determination of rice productivity. To explore the underlying genetic basis of grain number in rice, quantitative trait locus (QTL) analysis was performed using three recombinant inbred line populations derived from indica rice crosses of Teqing/IRBB lines, Zhenshan 97/Milyang 46, and Xieqingzao/Milyang 46, respectively. A total of 58 QTLs distributed on all 12 rice chromosomes were identified, including 22 for number of grains per panicle (NGP), 17 for number of spikelets per panicle, and 19 for spikelet fertility. The individual QTL counted for 1.5 to 22.1% of phenotypic variation. Among them, 15 QTLs shared by two or three populations and eight QTLs showed large effects with R2 larger than 10%. Furthermore, three QTLs with minor effects for NGP, qNGP5.5, qNGP9.1, and qNGP12.1, were detected and validated by eliminating the segregation of major-effect QTL using four residual heterozygote-derived populations. These results not only enrich our understanding of the mechanism of grain number, but also provide a foundation for cloning and selecting candidate for marker-assisted selection breeding in rice. [ABSTRACT FROM AUTHOR]