ID 57453
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Author
Tanaka, Tsuyoshi Breeding Informatics Research Unit, Division of Basic Research, Institute of Crop Science, National Agriculture and Food Research Organization (NARO),
Ishikawa, Goro Breeding Strategies Research Unit, Division of Basic Research, Institute of Crop Science, National Agriculture and Food Research Organization (NARO)
Ogiso-Tanaka, Eri Soybean and Field Crop Applied Genomics Research Unit, Division of Field Crop Research, Institute of Crop Science, National Agriculture and Food Research Organization (NARO)
Yanagisawa, Takashi Wheat and Barley Breeding Unit, Division of Wheat and Barley Research, Institute of Crop Science, National Agriculture and Food Research Organization (NARO)
Sato, Kazuhiro Group of Genome Diversity, Institute of Plant Science and Resources, Okayama University Kaken ID
Abstract
Marker-assisted selection of crop plants requires DNA markers that can distinguish between the closely related strains often used in breeding. The availability of reference genome sequence facilitates the generation of markers, by elucidating the genomic positions of new markers as well as of their neighboring sequences. In 2017, a high quality genome sequence was released for the six-row barley (Hordeum vulgare) cultivar Morex. Here, we developed a de novo RNA-Seq-based genotyping procedure for barley strains used in Japanese breeding programs. Using RNA samples from the seedling shoot, seedling root, and immature flower spike, we mapped next-generation sequencing reads onto the transcribed regions, which correspond to ∼590 Mb of the whole ∼4.8-Gbp reference genome sequence. Using 150 samples from 108 strains, we detected 181,567 SNPs and 45,135 indels located in the 28,939 transcribed regions distributed throughout the Morex genome. We evaluated the quality of this polymorphism detection approach by analyzing 387 RNA-Seq-derived SNPs using amplicon sequencing. More than 85% of the RNA-Seq SNPs were validated using the highly redundant reads from the amplicon sequencing, although half of the indels and multiple-allele loci showed different polymorphisms between the platforms. These results demonstrated that our RNA-Seq-based de novo polymorphism detection system generates genome-wide markers, even in the closely related barley genotypes used in breeding programs.
Keywords
Japanese barley breeding
RNA-Seq
amplicon sequencing
barley; genotyping
barley
genotyping
Published Date
2019-05-10
Publication Title
Frontiers in plant science.
Volume
volume577
Publisher
Frontiers Research Foundation
Start Page
577
ISSN
1664-462X
Content Type
Journal Article
language
英語
OAI-PMH Set
岡山大学
Copyright Holders
Copyright © 2019 Tanaka, Ishikawa, Ogiso-Tanaka, Yanagisawa and Sato.
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PubMed ID
DOI
Related Url
isVersionOf https://doi.org/10.3389/fpls.2019.00577
License
http://creativecommons.org/licenses/by/4.0/
Citation
Tanaka T, Ishikawa G, Ogiso-Tanaka E, Yanagisawa T and Sato K (2019) Development of Genome-Wide SNP Markers for Barley via Reference- Based RNA-Seq Analysis. Front. Plant Sci. 10:577. doi: 10.3389/fpls.2019.00577