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Identification of accession-specific variants and development of KASP markers for assessing the genetic makeup of Brassica rapa seeds
BACKGROUND: Most crop seeds are F1 hybrids. Seed providers and plant breeders must be confident that the seed supplied to growers is of known, and uniform, genetic makeup. This requires maintenance of pure genotypes of the parental lines and testing to ensure the genetic purity of the F1 seed. Tradi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036802/ https://www.ncbi.nlm.nih.gov/pubmed/35468724 http://dx.doi.org/10.1186/s12864-022-08567-9 |
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author | Hong, Seongmin Choi, Su Ryun Kim, Jihyeong Jeong, Young-Min Kim, Ju-Sang Ahn, Chun-Hee Kwon, Suk-Yoon Lim, Yong Pyo Shin, Ah-Young Kim, Yong-Min |
author_facet | Hong, Seongmin Choi, Su Ryun Kim, Jihyeong Jeong, Young-Min Kim, Ju-Sang Ahn, Chun-Hee Kwon, Suk-Yoon Lim, Yong Pyo Shin, Ah-Young Kim, Yong-Min |
author_sort | Hong, Seongmin |
collection | PubMed |
description | BACKGROUND: Most crop seeds are F1 hybrids. Seed providers and plant breeders must be confident that the seed supplied to growers is of known, and uniform, genetic makeup. This requires maintenance of pure genotypes of the parental lines and testing to ensure the genetic purity of the F1 seed. Traditionally, seed purity has been assessed with a grow-out test (GOT) in the field, a time consuming and costly venture. Early in the last decade, seed testing with molecular markers was introduced as a replacement for GOT, and Kompetitive allele specific PCR (KASP) markers were recognized as promising tools for genetic testing of seeds. However, the markers available at that time could be inaccurate and applicable to only a small number of accessions or varieties due to the limited genetic information and reference genomes available. RESULTS: We identified 4,925,742 SNPs in 50 accessions of the Brasscia rapa core collection. From these, we identified 2,925 SNPs as accession-specific, considering properties of flanking region harboring accession-specific SNPs and genic region conservation among accessions by the Next Generation Sequencing (NGS) analysis. In total, 100 accession-specific markers were developed as accession-specific KASP markers. Based on the results of our validation experiments, the accession-specific markers successfully distinguised individuals from the mixed population including 50 target accessions from B. rapa core collection and the outgroup. Additionally, the marker set we developed here discriminated F1 hybrids and their parental lines with distinct clusters. CONCLUSIONS: This study provides efficient methods for developing KASP markers to distinguish individuals from the mixture comprised of breeding lines and germplasms from the resequencing data of Chinese cabbage (Brassica rapa spp. pekinensis). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-08567-9. |
format | Online Article Text |
id | pubmed-9036802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-90368022022-04-26 Identification of accession-specific variants and development of KASP markers for assessing the genetic makeup of Brassica rapa seeds Hong, Seongmin Choi, Su Ryun Kim, Jihyeong Jeong, Young-Min Kim, Ju-Sang Ahn, Chun-Hee Kwon, Suk-Yoon Lim, Yong Pyo Shin, Ah-Young Kim, Yong-Min BMC Genomics Research BACKGROUND: Most crop seeds are F1 hybrids. Seed providers and plant breeders must be confident that the seed supplied to growers is of known, and uniform, genetic makeup. This requires maintenance of pure genotypes of the parental lines and testing to ensure the genetic purity of the F1 seed. Traditionally, seed purity has been assessed with a grow-out test (GOT) in the field, a time consuming and costly venture. Early in the last decade, seed testing with molecular markers was introduced as a replacement for GOT, and Kompetitive allele specific PCR (KASP) markers were recognized as promising tools for genetic testing of seeds. However, the markers available at that time could be inaccurate and applicable to only a small number of accessions or varieties due to the limited genetic information and reference genomes available. RESULTS: We identified 4,925,742 SNPs in 50 accessions of the Brasscia rapa core collection. From these, we identified 2,925 SNPs as accession-specific, considering properties of flanking region harboring accession-specific SNPs and genic region conservation among accessions by the Next Generation Sequencing (NGS) analysis. In total, 100 accession-specific markers were developed as accession-specific KASP markers. Based on the results of our validation experiments, the accession-specific markers successfully distinguised individuals from the mixed population including 50 target accessions from B. rapa core collection and the outgroup. Additionally, the marker set we developed here discriminated F1 hybrids and their parental lines with distinct clusters. CONCLUSIONS: This study provides efficient methods for developing KASP markers to distinguish individuals from the mixture comprised of breeding lines and germplasms from the resequencing data of Chinese cabbage (Brassica rapa spp. pekinensis). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-08567-9. BioMed Central 2022-04-25 /pmc/articles/PMC9036802/ /pubmed/35468724 http://dx.doi.org/10.1186/s12864-022-08567-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visithttp://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Hong, Seongmin Choi, Su Ryun Kim, Jihyeong Jeong, Young-Min Kim, Ju-Sang Ahn, Chun-Hee Kwon, Suk-Yoon Lim, Yong Pyo Shin, Ah-Young Kim, Yong-Min Identification of accession-specific variants and development of KASP markers for assessing the genetic makeup of Brassica rapa seeds |
title | Identification of accession-specific variants and development of KASP markers for assessing the genetic makeup of Brassica rapa seeds |
title_full | Identification of accession-specific variants and development of KASP markers for assessing the genetic makeup of Brassica rapa seeds |
title_fullStr | Identification of accession-specific variants and development of KASP markers for assessing the genetic makeup of Brassica rapa seeds |
title_full_unstemmed | Identification of accession-specific variants and development of KASP markers for assessing the genetic makeup of Brassica rapa seeds |
title_short | Identification of accession-specific variants and development of KASP markers for assessing the genetic makeup of Brassica rapa seeds |
title_sort | identification of accession-specific variants and development of kasp markers for assessing the genetic makeup of brassica rapa seeds |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036802/ https://www.ncbi.nlm.nih.gov/pubmed/35468724 http://dx.doi.org/10.1186/s12864-022-08567-9 |
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