Detection of QTLs controlling alpha-amylase activity in a diversity panel of 343 barley accessions
Autor: | Makoto Kihara, Kazuhiro Sato, Tian Su Zhou, Hiroshi Hisano, Satoko Matsumoto |
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Rok vydání: | 2018 |
Předmět: |
0106 biological sciences
0301 basic medicine Alpha-amylase activity Haplotype food and beverages Chromosome Single-nucleotide polymorphism Plant Science Biology Quantitative trait locus 01 natural sciences 03 medical and health sciences Horticulture 030104 developmental biology Genotype Genetics High activity Allele Agronomy and Crop Science Molecular Biology 010606 plant biology & botany Biotechnology |
Zdroj: | Molecular Breeding. 38 |
ISSN: | 1572-9788 1380-3743 |
DOI: | 10.1007/s11032-017-0773-y |
Popis: | The α–amylase activity of cultivated barley is critically important to the brewing industry. Here, we surveyed variation in malt α–amylase activity in 343 cultivated barley accessions from around the world. Population structure analysis based on genotype data at 1536 SNPs clustered these accessions into two groups, one comprising South-East Asian and Ethiopian accessions and one group containing the other accessions. A genome-wide association study identified significant quantitative trait loci (QTLs) for α–amylase activity on all seven chromosomes of barley. Accessions showing high and low α–amylase activity were crossed with the high-quality Japanese malting barley cv. Harun Nijo to develop F2 mapping populations. We identified two QTLs on chromosome 6H in a cross between Haruna Nijo (high activity) × Weal (highest activity). Single QTLs were identified each on 3H, 4H, and 5H from a cross between Haruna Nijo (high activity) × VLB-1 (low activity), indicating that the high α–amylase activity in Haruna Nijo might be derived from loci on these chromosomes. The addition of the high α–amylase activity QTL alleles from chromosome 6H in cv. Weal further increased the α–amylase activity conferred by alleles of Haruna Nijo. These results demonstrate that a target haplotype can be successfully improved using a strategy comprising diversity analysis of ex situ collections followed by introducing effective new alleles. |
Databáze: | OpenAIRE |
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