Identification and candidate analysis of a new brown planthopper resistance locus in an Indian landrace of rice, paedai kalibungga
The brown planthopper ( Nilaparvata lugens Stål, BPH) is the most destructive pest of rice ( Oryza sativa L.). Utilizing resistant rice cultivars that harbor resistance gene/s is an effective strategy for integrated pest management. Due to the co-evolution of BPH and rice, a single resistance gene m...
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Veröffentlicht in: | Molecular breeding 2024-07, Vol.44 (7), p.45-45, Article 45 |
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Zusammenfassung: | The brown planthopper (
Nilaparvata lugens
Stål, BPH) is the most destructive pest of rice (
Oryza sativa
L.). Utilizing resistant rice cultivars that harbor resistance gene/s is an effective strategy for integrated pest management. Due to the co-evolution of BPH and rice, a single resistance gene may fail because of changes in the virulent BPH population. Thus, it is urgent to explore and map novel BPH resistance genes in rice germplasm. Previously, an
indica
landrace from India, Paedai kalibungga (PK), demonstrated high resistance to BPH in both in Wuhan and Fuzhou, China. To map BPH resistance genes from PK, a BC
1
F
2:3
population derived from crosses of PK and a susceptible parent, Zhenshan 97 (ZS97), was developed and evaluated for BPH resistance. A novel BPH resistance locus,
BPH39
, was mapped on the short arm of rice chromosome 6 using next-generation sequencing-based bulked segregant analysis (BSA-seq).
BPH39
was validated using flanking markers within the locus. Furthermore, near-isogenic lines carrying
BPH39
(NIL-BPH39) were developed in the ZS97 background. NIL-BPH39 exhibited the physiological mechanisms of antibiosis and preference toward BPH.
BPH39
was finally delimited to an interval of 84 Kb ranging from 1.07 to 1.15 Mb. Six candidate genes were identified in this region. Two of them (
LOC_Os06g02930
and
LOC_Os06g03030
) encode proteins with a similar short consensus repeat (SCR) domain, which displayed many variations leading to amino acid substitutions and showed higher expression levels in NIL-BPH39. Thus, these two genes are considered reliable candidate genes for
BPH3
9. Additionally, transcriptome sequencing, DEGs analysis, and gene RT-qPCR verification preliminary revealed that
BPH39
may be involved in the jasmonic acid (JA) signaling pathway, thus mediating the molecular mechanism of BPH resistance. This work will facilitate map-based cloning and marker-assisted selection for the locus in breeding programs targeting BPH resistance. |
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ISSN: | 1380-3743 1572-9788 1572-9788 |
DOI: | 10.1007/s11032-024-01485-6 |