Genomic-Assisted Marker Development Suitable for CsCvy-1 Selection in Cucumber Breeding


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Kahveci E., Devran Z., oezkaynak E., Hong Y., Studholme D. J., Toer M.

FRONTIERS IN PLANT SCIENCE, cilt.12, 2021 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 12
  • Basım Tarihi: 2021
  • Doi Numarası: 10.3389/fpls.2021.691576
  • Dergi Adı: FRONTIERS IN PLANT SCIENCE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, BIOSIS, Directory of Open Access Journals
  • Anahtar Kelimeler: CVYV, cucumber, marker assisted selection, kompetitive allele-specific PCR genotyping, plant breeding, VEIN-YELLOWING-VIRUS, INNATE IMMUNITY, BIOLOGICAL-CONTROL, RESISTANCE GENES, BEMISIA-TABACI, SEQUENCE, DISEASE, MEMBER
  • Akdeniz Üniversitesi Adresli: Evet

Özet

Cucumber is a widely grown vegetable crop plant and a host to many different plant pathogens. Cucumber vein yellowing virus (CVYV) causes economic losses on cucumber crops in Mediterranean countries and in some part of India such as West Bengal and in African countries such as Sudan. CVYV is an RNA potyvirus transmitted mechanically and by whitefly (Bemisia tabaci) in a semipersistent manner. Control of this virus is heavily dependent on the management of the insect vector and breeding virus-resistant lines. DNA markers have been used widely in conventional plant breeding programs via marker-assisted selection (MAS). However, very few resistance sources against CVYV in cucumber exist, and also the lack of tightly linked molecular markers to these sources restricts the rapid generation of resistant lines. In this work, we used genomics coupled with the bulked segregant analysis method and generated the MAS-friendly Kompetitive allele specific PCR (KASP) markers suitable for CsCvy-1 selection in cucumber breeding using a segregating F-2 mapping population and commercial plant lines. Variant analysis was performed to generate single-nucleotide polymorphism (SNP)-based markers for mapping the population and genotyping the commercial lines. We fine-mapped the region by generating new markers down to 101 kb with eight genes. We provided SNP data for this interval, which could be useful for breeding programs and cloning the candidate genes.