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Development of AhMITE1 markers through genome-wide analysis in peanut (Arachis hypogaea L.)
OBJECTIVE: In peanut, the DNA polymorphism is very low despite enormous phenotypic variations. This limits the use of genomics-assisted breeding to enhance peanut productivity. This study aimed to develop and validate new AhMITE1 and cleaved amplified polymorphic sequences (CAPS) markers. RESULTS: I...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5759262/ https://www.ncbi.nlm.nih.gov/pubmed/29310707 http://dx.doi.org/10.1186/s13104-017-3121-8 |
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author | Gayathri, M. Shirasawa, Kenta Varshney, R. K. Pandey, M. K. Bhat, R. S. |
author_facet | Gayathri, M. Shirasawa, Kenta Varshney, R. K. Pandey, M. K. Bhat, R. S. |
author_sort | Gayathri, M. |
collection | PubMed |
description | OBJECTIVE: In peanut, the DNA polymorphism is very low despite enormous phenotypic variations. This limits the use of genomics-assisted breeding to enhance peanut productivity. This study aimed to develop and validate new AhMITE1 and cleaved amplified polymorphic sequences (CAPS) markers. RESULTS: In total, 2957 new AhMITE1 markers were developed in addition to identifying 465 already reported markers from the whole genome re-sequencing data (WGRS) of 33 diverse genotypes of peanut. The B sub-genome (1620) showed more number of markers than the A sub-genome (1337). Distribution also varied among the chromosomes of both the sub-genomes. Further, 52.6% of the markers were from genic regions; where 31.0% were from intronic regions and 5.2% were from exonic regions. Of the 343 randomly selected markers, 82.2% showed amplification validation, with up to 35.5% polymorphism. From the SNPs on the A03, B01, B02 and B03 chromosomes, 11,730 snip-SNPs (potential CAPS sites) were identified, and 500 CAPS markers were developed from chromosome A03. Of these markers, 30.0% showed validation and high polymorphism. This study demonstrated the potential of the WGRS data to develop AhMITE1 and CAPS markers, which showed high level of validation and polymorphism. These marker resources will be useful for various genetic studies and mapping in peanut. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13104-017-3121-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5759262 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57592622018-01-10 Development of AhMITE1 markers through genome-wide analysis in peanut (Arachis hypogaea L.) Gayathri, M. Shirasawa, Kenta Varshney, R. K. Pandey, M. K. Bhat, R. S. BMC Res Notes Research Note OBJECTIVE: In peanut, the DNA polymorphism is very low despite enormous phenotypic variations. This limits the use of genomics-assisted breeding to enhance peanut productivity. This study aimed to develop and validate new AhMITE1 and cleaved amplified polymorphic sequences (CAPS) markers. RESULTS: In total, 2957 new AhMITE1 markers were developed in addition to identifying 465 already reported markers from the whole genome re-sequencing data (WGRS) of 33 diverse genotypes of peanut. The B sub-genome (1620) showed more number of markers than the A sub-genome (1337). Distribution also varied among the chromosomes of both the sub-genomes. Further, 52.6% of the markers were from genic regions; where 31.0% were from intronic regions and 5.2% were from exonic regions. Of the 343 randomly selected markers, 82.2% showed amplification validation, with up to 35.5% polymorphism. From the SNPs on the A03, B01, B02 and B03 chromosomes, 11,730 snip-SNPs (potential CAPS sites) were identified, and 500 CAPS markers were developed from chromosome A03. Of these markers, 30.0% showed validation and high polymorphism. This study demonstrated the potential of the WGRS data to develop AhMITE1 and CAPS markers, which showed high level of validation and polymorphism. These marker resources will be useful for various genetic studies and mapping in peanut. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13104-017-3121-8) contains supplementary material, which is available to authorized users. BioMed Central 2018-01-08 /pmc/articles/PMC5759262/ /pubmed/29310707 http://dx.doi.org/10.1186/s13104-017-3121-8 Text en © The Author(s) 2018 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 | Research Note Gayathri, M. Shirasawa, Kenta Varshney, R. K. Pandey, M. K. Bhat, R. S. Development of AhMITE1 markers through genome-wide analysis in peanut (Arachis hypogaea L.) |
title | Development of AhMITE1 markers through genome-wide analysis in peanut (Arachis hypogaea L.) |
title_full | Development of AhMITE1 markers through genome-wide analysis in peanut (Arachis hypogaea L.) |
title_fullStr | Development of AhMITE1 markers through genome-wide analysis in peanut (Arachis hypogaea L.) |
title_full_unstemmed | Development of AhMITE1 markers through genome-wide analysis in peanut (Arachis hypogaea L.) |
title_short | Development of AhMITE1 markers through genome-wide analysis in peanut (Arachis hypogaea L.) |
title_sort | development of ahmite1 markers through genome-wide analysis in peanut (arachis hypogaea l.) |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5759262/ https://www.ncbi.nlm.nih.gov/pubmed/29310707 http://dx.doi.org/10.1186/s13104-017-3121-8 |
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