<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kumar R</submitter><funding>National Institute of Food and Agriculture</funding><pagination>299</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12596284</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>138(12)</volume><pubmed_abstract>&lt;h4>Key message&lt;/h4>A major QTL conferring powdery mildew resistance was fine mapped to a 54.8 kb region on chromosome 2 using an interspecific RIL population (Citrullus mucosospermus × Citrullus lanatus). Four co-segregating KASP markers were developed and validated across multiple populations, demonstrating their utility for marker-assisted selection. Powdery mildew, caused by Podosphaera xanthii, is a major fungal disease that significantly affects watermelon production worldwide. Developing resistant cultivars through marker-assisted selection (MAS) offers an effective and sustainable strategy for disease management. In this study, a 54,772 bp quantitative trait locus (QTL) associated with powdery mildew resistance was mapped to chromosome 2 (30,111,475-30,166,247 bp) using an F&lt;sub>11&lt;/sub> recombinant inbred line (RIL) population derived from an interspecific cross between the resistant C. mucosospermus line USVL531-MDR and the susceptible C. lanatus line USVL677-PMS. Genetic analysis revealed that resistance is controlled by a single dominant gene, supported by a 3:1 segregation ratio observed in F&lt;sub>2&lt;/sub> populations. The mapped region harbored three lipoxygenase (LOX) genes and one 50S ribosomal protein L27-like gene. Four KASP markers were developed from SNPs located within four putative genes in the QTL region and were validated across multiple segregating populations, including the RIL (USVL531-MDR × USVL677-PMS) and two F&lt;sub>2&lt;/sub> populations (USVL531-MDR × 'Sugar Baby' and PI 560003 × USVL677-PMS). These markers accurately differentiated resistant and susceptible individuals (R2 = 0.68-0.82) and exhibited 100% co-segregation with powdery mildew resistance in the RIL and two F&lt;sub>2&lt;/sub> populations, demonstrating their utility for MAS. The identified QTL and validated KASP markers will facilitate MAS for powdery mildew resistance breeding and enable future gene cloning work.</pubmed_abstract><journal>TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik</journal><pubmed_title>Fine mapping, introgression, and KASP marker development for powdery mildew resistance in watermelon using an interspecific RIL population (Citrullus mucosospermus × C. lanatus).</pubmed_title><pmcid>PMC12596284</pmcid><funding_grant_id>2015-51181-24285</funding_grant_id><funding_grant_id>2020-51181-32139</funding_grant_id><pubmed_authors>Karthikeyan R</pubmed_authors><pubmed_authors>Ikerd J</pubmed_authors><pubmed_authors>Kumar R</pubmed_authors><pubmed_authors>Kousik C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Fine mapping, introgression, and KASP marker development for powdery mildew resistance in watermelon using an interspecific RIL population (Citrullus mucosospermus × C. lanatus).</name><description>&lt;h4>Key message&lt;/h4>A major QTL conferring powdery mildew resistance was fine mapped to a 54.8 kb region on chromosome 2 using an interspecific RIL population (Citrullus mucosospermus × Citrullus lanatus). Four co-segregating KASP markers were developed and validated across multiple populations, demonstrating their utility for marker-assisted selection. Powdery mildew, caused by Podosphaera xanthii, is a major fungal disease that significantly affects watermelon production worldwide. Developing resistant cultivars through marker-assisted selection (MAS) offers an effective and sustainable strategy for disease management. In this study, a 54,772 bp quantitative trait locus (QTL) associated with powdery mildew resistance was mapped to chromosome 2 (30,111,475-30,166,247 bp) using an F&lt;sub>11&lt;/sub> recombinant inbred line (RIL) population derived from an interspecific cross between the resistant C. mucosospermus line USVL531-MDR and the susceptible C. lanatus line USVL677-PMS. Genetic analysis revealed that resistance is controlled by a single dominant gene, supported by a 3:1 segregation ratio observed in F&lt;sub>2&lt;/sub> populations. The mapped region harbored three lipoxygenase (LOX) genes and one 50S ribosomal protein L27-like gene. Four KASP markers were developed from SNPs located within four putative genes in the QTL region and were validated across multiple segregating populations, including the RIL (USVL531-MDR × USVL677-PMS) and two F&lt;sub>2&lt;/sub> populations (USVL531-MDR × 'Sugar Baby' and PI 560003 × USVL677-PMS). These markers accurately differentiated resistant and susceptible individuals (R2 = 0.68-0.82) and exhibited 100% co-segregation with powdery mildew resistance in the RIL and two F&lt;sub>2&lt;/sub> populations, demonstrating their utility for MAS. The identified QTL and validated KASP markers will facilitate MAS for powdery mildew resistance breeding and enable future gene cloning work.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-06-06T13:28:16.312Z</modification><creation>2026-05-31T03:08:03.164Z</creation></dates><accession>S-EPMC12596284</accession><cross_references><pubmed>41205047</pubmed><doi>10.1007/s00122-025-05079-4</doi></cross_references></HashMap>