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Mango (Mangifera indica L.) germplasm diversity based on single nucleotide polymorphisms derived from the transcriptome
BACKGROUND: Germplasm collections are an important source for plant breeding, especially in fruit trees which have a long duration of juvenile period. Thus, efforts have been made to study the diversity of fruit tree collections. Even though mango is an economically important crop, most of the studi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4647706/ https://www.ncbi.nlm.nih.gov/pubmed/26573148 http://dx.doi.org/10.1186/s12870-015-0663-6 |
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author | Sherman, Amir Rubinstein, Mor Eshed, Ravit Benita, Miri Ish-Shalom, Mazal Sharabi-Schwager, Michal Rozen, Ada Saada, David Cohen, Yuval Ophir, Ron |
author_facet | Sherman, Amir Rubinstein, Mor Eshed, Ravit Benita, Miri Ish-Shalom, Mazal Sharabi-Schwager, Michal Rozen, Ada Saada, David Cohen, Yuval Ophir, Ron |
author_sort | Sherman, Amir |
collection | PubMed |
description | BACKGROUND: Germplasm collections are an important source for plant breeding, especially in fruit trees which have a long duration of juvenile period. Thus, efforts have been made to study the diversity of fruit tree collections. Even though mango is an economically important crop, most of the studies on diversity in mango collections have been conducted with a small number of genetic markers. RESULTS: We describe a de novo transcriptome assembly from mango cultivar ‘Keitt’. Variation discovery was performed using Illumina resequencing of ‘Keitt’ and ‘Tommy Atkins’ cultivars identified 332,016 single-nucleotide polymorphisms (SNPs) and 1903 simple-sequence repeats (SSRs). Most of the SSRs (70.1 %) were of trinucleotide with the preponderance of motif (GGA/AAG)n and only 23.5 % were di-nucleotide SSRs with the mostly of (AT/AT)n motif. Further investigation of the diversity in the Israeli mango collection was performed based on a subset of 293 SNPs. Those markers have divided the Israeli mango collection into two major groups: one group included mostly mango accessions from Southeast Asia (Malaysia, Thailand, Indonesia) and India and the other with mainly of Floridian and Israeli mango cultivars. The latter group was more polymorphic (F(S) = −0.1 on the average) and was more of an admixture than the former group. A slight population differentiation was detected (F(ST) = 0.03), suggesting that if the mango accessions of the western world apparently was originated from Southeast Asia, as has been previously suggested, the duration of cultivation was not long enough to develop a distinct genetic background. CONCLUSIONS: Whole-transcriptome reconstruction was used to significantly broaden the mango’s genetic variation resources, i.e., SNPs and SSRs. The set of SNP markers described in this study is novel. A subset of SNPs was sampled to explore the Israeli mango collection and most of them were polymorphic in many mango accessions. Therefore, we believe that these SNPs will be valuable as they recapitulate and strengthen the history of mango diversity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-015-0663-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4647706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46477062015-11-18 Mango (Mangifera indica L.) germplasm diversity based on single nucleotide polymorphisms derived from the transcriptome Sherman, Amir Rubinstein, Mor Eshed, Ravit Benita, Miri Ish-Shalom, Mazal Sharabi-Schwager, Michal Rozen, Ada Saada, David Cohen, Yuval Ophir, Ron BMC Plant Biol Research Article BACKGROUND: Germplasm collections are an important source for plant breeding, especially in fruit trees which have a long duration of juvenile period. Thus, efforts have been made to study the diversity of fruit tree collections. Even though mango is an economically important crop, most of the studies on diversity in mango collections have been conducted with a small number of genetic markers. RESULTS: We describe a de novo transcriptome assembly from mango cultivar ‘Keitt’. Variation discovery was performed using Illumina resequencing of ‘Keitt’ and ‘Tommy Atkins’ cultivars identified 332,016 single-nucleotide polymorphisms (SNPs) and 1903 simple-sequence repeats (SSRs). Most of the SSRs (70.1 %) were of trinucleotide with the preponderance of motif (GGA/AAG)n and only 23.5 % were di-nucleotide SSRs with the mostly of (AT/AT)n motif. Further investigation of the diversity in the Israeli mango collection was performed based on a subset of 293 SNPs. Those markers have divided the Israeli mango collection into two major groups: one group included mostly mango accessions from Southeast Asia (Malaysia, Thailand, Indonesia) and India and the other with mainly of Floridian and Israeli mango cultivars. The latter group was more polymorphic (F(S) = −0.1 on the average) and was more of an admixture than the former group. A slight population differentiation was detected (F(ST) = 0.03), suggesting that if the mango accessions of the western world apparently was originated from Southeast Asia, as has been previously suggested, the duration of cultivation was not long enough to develop a distinct genetic background. CONCLUSIONS: Whole-transcriptome reconstruction was used to significantly broaden the mango’s genetic variation resources, i.e., SNPs and SSRs. The set of SNP markers described in this study is novel. A subset of SNPs was sampled to explore the Israeli mango collection and most of them were polymorphic in many mango accessions. Therefore, we believe that these SNPs will be valuable as they recapitulate and strengthen the history of mango diversity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-015-0663-6) contains supplementary material, which is available to authorized users. BioMed Central 2015-11-14 /pmc/articles/PMC4647706/ /pubmed/26573148 http://dx.doi.org/10.1186/s12870-015-0663-6 Text en © Sherman et al. 2015 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 Article Sherman, Amir Rubinstein, Mor Eshed, Ravit Benita, Miri Ish-Shalom, Mazal Sharabi-Schwager, Michal Rozen, Ada Saada, David Cohen, Yuval Ophir, Ron Mango (Mangifera indica L.) germplasm diversity based on single nucleotide polymorphisms derived from the transcriptome |
title | Mango (Mangifera indica L.) germplasm diversity based on single nucleotide polymorphisms derived from the transcriptome |
title_full | Mango (Mangifera indica L.) germplasm diversity based on single nucleotide polymorphisms derived from the transcriptome |
title_fullStr | Mango (Mangifera indica L.) germplasm diversity based on single nucleotide polymorphisms derived from the transcriptome |
title_full_unstemmed | Mango (Mangifera indica L.) germplasm diversity based on single nucleotide polymorphisms derived from the transcriptome |
title_short | Mango (Mangifera indica L.) germplasm diversity based on single nucleotide polymorphisms derived from the transcriptome |
title_sort | mango (mangifera indica l.) germplasm diversity based on single nucleotide polymorphisms derived from the transcriptome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4647706/ https://www.ncbi.nlm.nih.gov/pubmed/26573148 http://dx.doi.org/10.1186/s12870-015-0663-6 |
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