文献类型: 外文期刊
作者: Fan, Yeyang 1 ; Zhang, Zhenhua 1 ; Huang, Derun 1 ; Huang, Tingxu 2 ; Wang, Hongfei 2 ; Zhuang, Jieyun 1 ; Zhu, Yujun 1 ;
作者机构: 1.China Natl Rice Res Inst, State Key Lab Rice Biol & Breeding, Hangzhou 310006, Peoples R China
2.Fujian Acad Agr Sci, Rice Res Inst, HW, Fuzhou 350018, Peoples R China
关键词: rice blast; allele-specific marker; allele; tetra-primer amplification refractory mutation system (ARMS)-PCR; single nucleotide polymorphism; marker-assisted selection
期刊名称:AGRICULTURE-BASEL ( 影响因子:3.6; 五年影响因子:3.6 )
ISSN:
年卷期: 2023 年 13 卷 10 期
页码:
收录情况: SCI
摘要: 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 (Pi25(TTP)) 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 (Pi25(GM2)) and the susceptible allele Pi25(TTP). 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.
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