Cargando…

Exome QTL-seq maps monogenic locus and QTLs in barley

BACKGROUND: QTL-seq, in combination with bulked segregant analysis and next-generation sequencing (NGS), is used to identify loci in small plant genomes, but is technically challenging to perform in species with large genomes, such as barley. A combination of exome sequencing and QTL-seq (exome QTL-...

Descripción completa

Detalles Bibliográficos
Autores principales: Hisano, Hiroshi, Sakamoto, Kazuki, Takagi, Hiroki, Terauchi, Ryohei, Sato, Kazuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288901/
https://www.ncbi.nlm.nih.gov/pubmed/28148242
http://dx.doi.org/10.1186/s12864-017-3511-2
_version_ 1782504413848403968
author Hisano, Hiroshi
Sakamoto, Kazuki
Takagi, Hiroki
Terauchi, Ryohei
Sato, Kazuhiro
author_facet Hisano, Hiroshi
Sakamoto, Kazuki
Takagi, Hiroki
Terauchi, Ryohei
Sato, Kazuhiro
author_sort Hisano, Hiroshi
collection PubMed
description BACKGROUND: QTL-seq, in combination with bulked segregant analysis and next-generation sequencing (NGS), is used to identify loci in small plant genomes, but is technically challenging to perform in species with large genomes, such as barley. A combination of exome sequencing and QTL-seq (exome QTL-seq) was used to map the mono-factorial Mendelian locus black lemma and pericarp (Blp) and QTLs for resistance to net blotch disease, a common disease of barley caused by the fungus Pyrenophora teres, which segregated in a population of 100 doubled haploid barley lines. METHODS: The provisional exome sequences were prepared by ordering the loci of expressed genes based on the genome information and concatenating genes with intervals of 200-bp spacer "N" for each chromosome. The QTL-seq pipeline was used to analyze short reads from the exome-captured library. RESULTS: In this study, short NGS reads of bulked total DNA samples from segregants with extreme trait values were subjected to exome capture, and the resulting exome sequences were aligned to the reference genome. SNP allele frequencies were compared to identify the locations of genes/QTLs responsible for the trait value differences between lines. For both objective traits examined, exome QTL-seq identified the monogenic Mendelian locus and associated QTLs. These findings were validated using conventional mapping approaches. CONCLUSIONS: Exome QTL-seq broadens the utility of NGS-based gene/QTL mapping in organisms with large genomes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3511-2) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5288901
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-52889012017-02-09 Exome QTL-seq maps monogenic locus and QTLs in barley Hisano, Hiroshi Sakamoto, Kazuki Takagi, Hiroki Terauchi, Ryohei Sato, Kazuhiro BMC Genomics Methodology Article BACKGROUND: QTL-seq, in combination with bulked segregant analysis and next-generation sequencing (NGS), is used to identify loci in small plant genomes, but is technically challenging to perform in species with large genomes, such as barley. A combination of exome sequencing and QTL-seq (exome QTL-seq) was used to map the mono-factorial Mendelian locus black lemma and pericarp (Blp) and QTLs for resistance to net blotch disease, a common disease of barley caused by the fungus Pyrenophora teres, which segregated in a population of 100 doubled haploid barley lines. METHODS: The provisional exome sequences were prepared by ordering the loci of expressed genes based on the genome information and concatenating genes with intervals of 200-bp spacer "N" for each chromosome. The QTL-seq pipeline was used to analyze short reads from the exome-captured library. RESULTS: In this study, short NGS reads of bulked total DNA samples from segregants with extreme trait values were subjected to exome capture, and the resulting exome sequences were aligned to the reference genome. SNP allele frequencies were compared to identify the locations of genes/QTLs responsible for the trait value differences between lines. For both objective traits examined, exome QTL-seq identified the monogenic Mendelian locus and associated QTLs. These findings were validated using conventional mapping approaches. CONCLUSIONS: Exome QTL-seq broadens the utility of NGS-based gene/QTL mapping in organisms with large genomes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3511-2) contains supplementary material, which is available to authorized users. BioMed Central 2017-02-02 /pmc/articles/PMC5288901/ /pubmed/28148242 http://dx.doi.org/10.1186/s12864-017-3511-2 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology Article
Hisano, Hiroshi
Sakamoto, Kazuki
Takagi, Hiroki
Terauchi, Ryohei
Sato, Kazuhiro
Exome QTL-seq maps monogenic locus and QTLs in barley
title Exome QTL-seq maps monogenic locus and QTLs in barley
title_full Exome QTL-seq maps monogenic locus and QTLs in barley
title_fullStr Exome QTL-seq maps monogenic locus and QTLs in barley
title_full_unstemmed Exome QTL-seq maps monogenic locus and QTLs in barley
title_short Exome QTL-seq maps monogenic locus and QTLs in barley
title_sort exome qtl-seq maps monogenic locus and qtls in barley
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288901/
https://www.ncbi.nlm.nih.gov/pubmed/28148242
http://dx.doi.org/10.1186/s12864-017-3511-2
work_keys_str_mv AT hisanohiroshi exomeqtlseqmapsmonogeniclocusandqtlsinbarley
AT sakamotokazuki exomeqtlseqmapsmonogeniclocusandqtlsinbarley
AT takagihiroki exomeqtlseqmapsmonogeniclocusandqtlsinbarley
AT terauchiryohei exomeqtlseqmapsmonogeniclocusandqtlsinbarley
AT satokazuhiro exomeqtlseqmapsmonogeniclocusandqtlsinbarley