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Globally-deployed sorghum aphid resistance gene RMES1 is vulnerable to biotype shifts but being bolstered by RMES2

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NIAID Data Ecosystem2026-05-01 收录
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http://datadryad.org/dataset/doi%253A10.5061%252Fdryad.rv15dv4f6
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Durable host plant resistance (HPR) to insect pests is critical for sustainable agriculture. Natural variation exists for aphid HPR in sorghum (Sorghum bicolor) but the genetic architecture and phenotype have not been clarified for most sources. To assess the threat of a sorghum aphid (Melanaphis sorghi) biotype shift, we characterized the phenotype of Resistance to Melanaphis sorghi 1 (RMES1) and contributing HPR architecture in globally-admixed populations selected under severe aphid infestation in Haiti. We developed and sequenced RMES1 near-isogenic lines and found RMES1 reduces sorghum aphid fecundity but not bird cherry-oat aphid (Rhopalosiphum padi) fecundity, suggesting a discriminant HPR response typical of gene-for-gene interaction. Analyzing whole-genome resequencing of a global diversity panel, we found resistant alleles at a second gene, RMES2, were more frequent than RMES1 resistant alleles in landraces and historic breeding lines. RMES2 contributes early and mid-season aphid resistance in a segregating F2 population, however, RMES1 was only significant with mid-season fitness. In a fixed population with high aphid resistance, RMES1 and RMES2 were selected for demonstrating a lack of significant antagonistic pleiotropy. Associations with resistance co-located with cyanogenic glucoside biosynthesis genes support additional HPR sources. Globally, therefore, a vulnerable HPR source (RMES1) is bolstered by a second common source of resistance in breeding programs (RMES2) which may be staving off a biotype shift. Methods NIL genome characterization - newly generated resequencing data of near-isogenic lines and their parents was used to determine the genomic contribution of NILs Resequencing SAP,BAP association - previously generated phenotype data (Poosapati et al., 2022) and resequencing data (Boatwright et al., 2022, LeBauer et al., 2020) was combined to newly generate marker-trait association data Haitian breeding population association - newly generated DART sequencing and phenotype data was used to generate marker-trait association data Geographic mapping - plotting allele information of RMES1 and RMES2 with geographic coordinates or breeding origin metadata
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2023-11-29
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