4.5 Article

Molecular mapping and transfer of a novel brown planthopper resistance gene bph42 from Oryza rufipogon (Griff.) To cultivated rice (Oryza sativa L.)

期刊

MOLECULAR BIOLOGY REPORTS
卷 49, 期 9, 页码 8597-8606

出版社

SPRINGER
DOI: 10.1007/s11033-022-07692-8

关键词

Brown planthopper; Oryza rufipogon; QTL mapping; Linkage map; Bulked segregant analysis; Marker-assisted selection

资金

  1. ICAR under the Project 'Molecular breeding for improvement of tolerance to biotic and abiotic stresses, yield and quality traits in Crops-Rice, Department of Biotechnology, New Delhi [BT/PR31, 75/ATGC/127/5/2019]
  2. Department of Science and Technology, New Delhi [CRG/2018/001833]

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This study successfully identified and transferred a novel BPH resistance gene, bph42, from wild rice species into elite rice cultivars. Through genetic mapping and QTL analysis, the location of this resistance gene on chromosome 4 was determined, providing important insights for future varietal release. The identified marker associated with bph42 can be efficiently used in marker-assisted selection for breeding BPH-resistant rice cultivars.
Background Brown planthopper (BPH), Nilaparvata lugens (Stal), is one of the most destructive pests of rice accounting for 52% of annual yield loss. The breakdown of resistance against known BPH biotypes necessitates the identification and deployment of new genes from diverse sources. The current study aimed at mapping and transfer of a novel BPH resistance gene from the wild species of rice O. rufipogon accession CR100441 to the elite rice cultivar against BPH biotype 4. Methods and Results The phenotypic screening against BPH biotype 4 was conducted using the standard seedbox screening technique (SSST). Inheritance study using damage score caused by BPH infestation at the seedling stage indicated the presence of a single major recessive gene with the segregation ratio of susceptible to resistant plants in 3:1 (210:66, chi(2)c = 0.17 <= chi(2)(0.05,1) = 3.84). The genotyping of the mapping population was done using polymorphic microsatellite markers between PR122 and O.rufipogon acc.CR100441 spanning all the 12 chromosomes of rice. A total of 537 SSR markers were used to map a BPH resistance gene (designated as bph42) on the short arm of chromosome 4 between RM16282 and RM6659. QTL analysis identified a peak marker RM16335 contributing 29% of the phenotypic variance at 40.76 LOD. Conclusions The identified marker co-segregates with the bph42 and hence could be efficiently used for marker-assisted selection (MAS) for the transfer of resistance into elite rice cultivars. The introgression lines with higher yield and BPH resistance were identified and are under advanced yield trails for further varietal release.

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