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Mapping of a major quantitative trait locus for bakanae disease resistance in rice by genome resequencing

Authors :
Tae Ho Kim
Hyun-Ju Kang
Song Lim Kim
Seung-Bum Lee
Jeong-Ho Baek
Hyeonso Ji
Kyung-Hwan Kim
Inchan Choi
Gang-Seob Lee
Seok Cheol Suh
Source :
Molecular genetics and genomics : MGG. 293(3)
Publication Year :
2017

Abstract

Bakanae disease (BD) has emerged as a serious threat in almost all rice cultivation regions worldwide. Nampyeong is a Korean japonica rice variety known to be resistant to BD. In this study, quantitative trait locus (QTL) mapping was performed with F2 and F3 plants derived from a cross between the Nampyeong variety and a susceptible Korean japonica line, DongjinAD. First, resequencing of Nampyeong and DongjinAD was performed, which identified 171,035 single nucleotide polymorphisms (SNPs) between the two parental varieties. Using these SNPs, 161 cleaved amplified polymorphic sequence (CAPS) markers and six derived CAPS markers were developed; then, a genetic map was constructed from the genotypes of 180 plants from the DongjinAD/Nampyeong F2 plants. The total length of the constructed genetic map was 1386 cM, with an average interval of 8.9 cM between markers. The BD mortality rates of each F3 family were measured by testing 40 F3 progenies using in vitro seedling screening method. QTL analysis based on the genetic map and mortality rate data revealed a major QTL, qFfR1, on rice chromosome 1. qFfR1 was located at 89.8 cM with a logarithm of the odds (LOD) score of 22.7. Further, there were three markers at this point: JNS01033, JNS01037, and JNS01041. A total of 15 genes were identified with annotations related to defense against plant diseases among the 179 genes in the qFfR1 interval at 95% probability, thereby providing potential candidate genes for qFfR1. qFfR1 and its closely linked markers will be useful in breeding rice varieties resistant to BD.

Details

ISSN :
16174623
Volume :
293
Issue :
3
Database :
OpenAIRE
Journal :
Molecular genetics and genomics : MGG
Accession number :
edsair.doi.dedup.....a0e237b1153a3b3016036ac11cbf750a