Identification and fine-mapping of a new resistance gene, Xa40, conferring resistance to bacterial blight races in rice (Oryza sativa L.)

被引:95
|
作者
Kim, Suk-Man [1 ,2 ]
Suh, Jung-Pil [3 ]
Qin, Yang [4 ]
Noh, Tae-Hwan [5 ]
Reinke, Russell F. [1 ,2 ]
Jena, Kshirod K. [1 ]
机构
[1] Int Rice Res Inst, Plant Breeding Genet & Biotechnol Div, Manila, Philippines
[2] Rural Dev Adm, Natl Inst Crop Sci, IRRI Korea Off, Wanju Gun 565851, Jeollabuk Do, South Korea
[3] Rural Dev Adm, Natl Inst Crop Sci, Cent Area Crop Breeding Res Div, Suwon 441857, South Korea
[4] Rural Dev Adm, Natl Acad Agr Sci, Biosafety Div, Jeonju 560500, South Korea
[5] Rural Dev Adm, Natl Inst Crop Sci, Wanju Gun 565851, Jeollabuk Do, South Korea
关键词
WALL-ASSOCIATED KINASES; NBS-LRR PROTEINS; DISEASE RESISTANCE; XANTHOMONAS-ORYZAE; RECEPTOR KINASE; PV; ORYZAE; EXPRESSION; INHERITANCE; CULTIVARS; PATHOGEN;
D O I
10.1007/s00122-015-2557-2
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
A new bacterial blight resistance gene has been identified through fine-mapping, which confers high levels of resistance to all Korean Xanthomonas oryzae pv. oryzae ( Xoo ) races, including the new Xoo race K3a. Rice bacterial leaf blight (BB) disease caused by Xanthomonas oryzae pv. oryzae (Xoo) is a serious constraint to rice production in Asia and Africa. The japonica advanced backcross breeding lines derived from the indica line IR65482-7-216-1-2 in the background of cultivar Junam are resistant to all Korean BB races, including K3a. To identify the gene(s) involved in resistance to Korean Xoo races, the association of genotypic and phenotypic variations was examined in two F-2 populations derived from the crosses between 11325 (IR83261-3-7-23-6-2-1-1-2-1-2)/Anmi and 11325/Ilpum. The segregation ratios of F-2 individuals from the crosses of 11325/Anmi and 11325/Ilpum were 578 resistant:209 susceptible and 555 resistant:241 susceptible, respectively, which is consistent with the expected allelic frequency of a 3:1 ratio. Genetic analysis using graphical mapping indicated that resistance (R) was controlled by a new resistance gene linked with the flanking markers RM27320 and ID55.WA18-5 within an approximately 80-kb region between 28.14 and 28.22 Mbp on chromosome 11. The eight candidate genes functionally predicted were included in the target region. Examination of the candidate genes by RT-PCR analysis only corroborated with the significant difference in transcript levels of the WAK3 gene in the presence or absence of pathogen infection. Allelism tests performed with other known BB R-genes revealed that the allele was distinct from others having a similar chromosomal location.
引用
收藏
页码:1933 / 1943
页数:11
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