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An affordable and convenient diagnostic marker to identify male and female hop plants.
Clare, Shaun J; King, Ryan M; Tawril, Anna L; Havill, Joshua S; Muehlbauer, Gary J; Carey, Sarah B; Harkess, Alex; Bassil, Nahla; Altendorf, Kayla R.
Afiliação
  • Clare SJ; National Clonal Germplasm Repository, USDA-ARS, 33447 Peoria Road, Corvallis, OR 97333, USA.
  • King RM; National Clonal Germplasm Repository, USDA-ARS, 33447 Peoria Road, Corvallis, OR 97333, USA.
  • Tawril AL; Forage Seed and Cereal Research Unit, USDA-ARS, 24106 N Bunn Road, Prosser, WA 99350, USA.
  • Havill JS; Department of Agronomy and Plant Genetics, University of Minnesota, 1991 Upper Buford Circle, St.Paul, MN 55108, USA.
  • Muehlbauer GJ; Department of Agronomy and Plant Genetics, University of Minnesota, 1991 Upper Buford Circle, St.Paul, MN 55108, USA.
  • Carey SB; HudsonAlpha Institute for Biotechnology, 601 Genome Way Northwest, Huntsville, AL 35806, USA.
  • Harkess A; HudsonAlpha Institute for Biotechnology, 601 Genome Way Northwest, Huntsville, AL 35806, USA.
  • Bassil N; National Clonal Germplasm Repository, USDA-ARS, 33447 Peoria Road, Corvallis, OR 97333, USA.
  • Altendorf KR; Forage Seed and Cereal Research Unit, USDA-ARS, 24106 N Bunn Road, Prosser, WA 99350, USA.
G3 (Bethesda) ; 14(1)2023 Dec 29.
Article em En | MEDLINE | ID: mdl-37963231
Hop production utilizes exclusively female plants, whereas male plants only serve to generate novel variation within breeding programs through crossing. Currently, hop lacks a rapid and accurate diagnostic marker to determine whether plants are male or female. Without a diagnostic marker, breeding programs may take 1-2 years to determine the sex of new seedlings. Previous research on sex-linked markers was restricted to specific populations or breeding programs and therefore had limited transferability or suffered from low scalability. A large collection of 765 hop genotypes with known sex phenotypes, genotyping-by-sequencing, and genome-wide association mapping revealed a highly significant marker on the sex chromosome (LOD score = 208.7) that predicted sex within our population with 96.2% accuracy. In this study, we developed a PCR allele competitive extension (PACE) assay for the diagnostic SNP and tested three quick DNA extraction methodologies for rapid, high-throughput genotyping. Additionally, the marker was validated in a separate population of 94 individuals from 15 families from the USDA-ARS hop breeding program in Prosser, WA with 96% accuracy. This diagnostic marker is located in a gene predicted to encode the basic helix-loop-helix transcription factor protein, a family of proteins that have been previously implicated in male sterility in a variety of plant species, which may indicate a role in determining hop sex. The marker is diagnostic, accurate, affordable, and highly scalable and has the potential to improve efficiency in hop breeding.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estudo de Associação Genômica Ampla / Melhoramento Vegetal Limite: Humans Idioma: En Revista: G3 (Bethesda) Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estudo de Associação Genômica Ampla / Melhoramento Vegetal Limite: Humans Idioma: En Revista: G3 (Bethesda) Ano de publicação: 2023 Tipo de documento: Article