Author:
Ji Hyeonso,Kim Sung-Ryul,Kim Yul-Ho,Suh Jung-Pil,Park Hyang-Mi,Sreenivasulu Nese,Misra Gopal,Kim Suk-Man,Hechanova Sherry Lou,Kim Hakbum,Lee Gang-Seob,Yoon Ung-Han,Kim Tae-Ho,Lim Hyemin,Suh Suk-Chul,Yang Jungil,An Gynheung,Jena Kshirod K.
Abstract
Abstract
Brown planthopper (BPH) is a phloem sap-sucking insect pest of rice which causes severe yield loss. We cloned the BPH18 gene from the BPH-resistant introgression line derived from the wild rice species Oryza australiensis. Map-based cloning and complementation test revealed that the BPH18 encodes CC-NBS-NBS-LRR protein. BPH18 has two NBS domains, unlike the typical NBS-LRR proteins. The BPH18 promoter::GUS transgenic plants exhibited strong GUS expression in the vascular bundles of the leaf sheath, especially in phloem cells where the BPH attacks. The BPH18 proteins were widely localized to the endo-membranes in a cell, including the endoplasmic reticulum, Golgi apparatus, trans-Golgi network, and prevacuolar compartments, suggesting that BPH18 may recognize the BPH invasion at endo-membranes in phloem cells. Whole genome sequencing of the near-isogenic lines (NILs), NIL-BPH18 and NIL-BPH26, revealed that BPH18 located at the same locus of BPH26. However, these two genes have remarkable sequence differences and the independent NILs showed differential BPH resistance with different expression patterns of plant defense-related genes, indicating that BPH18 and BPH26 are functionally different alleles. These findings would facilitate elucidation of the molecular mechanism of BPH resistance and the identified novel alleles to fast track breeding BPH resistant rice cultivars.
Publisher
Springer Science and Business Media LLC
Cited by
126 articles.
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