Map-based Cloning and Characterization of a Brown Planthopper Resistance Gene BPH26 from Oryza sativa L. ssp indica Cultivar ADR52

被引:156
作者
Tamura, Yasumori [1 ]
Hattori, Makoto [1 ]
Yoshioka, Hirofumi [2 ]
Yoshioka, Miki [2 ]
Takahashi, Akira [3 ]
Wu, Jianzhong [4 ]
Sentoku, Naoki [5 ]
Yasui, Hideshi [6 ]
机构
[1] Natl Inst Agrobiol Sci, Div Insect Sci, Ibaraki 3058634, Japan
[2] Nagoya Univ, Lab Def Plant Pathogen Interact, Grad Sch Bioagr Sci, Nagoya, Aichi 4648601, Japan
[3] Natl Inst Agrobiol Sci, Genetically Modified Organism Res Ctr, Ibaraki 3058602, Japan
[4] Natl Inst Agrobiol Sci, Agrogen Res Ctr, Ibaraki 3058634, Japan
[5] Natl Inst Agrobiol Sci, Div Plant Sci, Ibaraki 3058604, Japan
[6] Kyushu Univ, Grad Sch, Plant Breeding Lab, Fac Agr, Fukuoka 8128581, Japan
来源
SCIENTIFIC REPORTS | 2014年 / 4卷
关键词
NILAPARVATA-LUGENS STAL; CONFERS RESISTANCE; MIGRATION ANALYSIS; PROBING BEHAVIOR; BARNYARD GRASS; LINKAGE MAP; RICE; DELPHACIDAE; HOMOPTERA; IDENTIFICATION;
D O I
10.1038/srep05872
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The brown planthopper (BPH) is the most serious insect pest of rice in Asia. The indica rice cultivar ADR52 carries two BPH resistance genes, BPH26 (BROWN PLANTHOPPER RESISTANCE 26) and BPH25. Map-based cloning of BPH26 revealed that BPH26 encodes a coiled-coil-nucleotide-binding-site-leucine-rich repeat (CC-NBS-LRR) protein. BPH26 mediated sucking inhibition in the phloem sieve element. BPH26 was identical to BPH2 on the basis of DNA sequence analysis and feeding ability of the BPH2-virulent biotype of BPH. BPH2 was widely incorporated in elite rice cultivars and was well-cultivated in many Asian countries as a favorable gene resource in rice breeding against BPH. However, BPH2 was rendered ineffective by a virulent biotype of BPH in rice fields in Asia. In this study, we suggest that BPH2 can be reused by combining with other BPH resistance genes, such as BPH25, to ensure durable resistance to BPH.
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页数:8
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