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Microsatellite marker development by partial sequencing of the sour passion fruit genome (Passiflora edulis Sims)

BACKGROUND: The Passiflora genus comprises hundreds of wild and cultivated species of passion fruit used for food, industrial, ornamental and medicinal purposes. Efforts to develop genomic tools for genetic analysis of P. edulis, the most important commercial Passiflora species, are still incipient....

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Autores principales: Araya, Susan, Martins, Alexandre M, Junqueira, Nilton T V, Costa, Ana Maria, Faleiro, Fábio G, Ferreira, Márcio E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520361/
https://www.ncbi.nlm.nih.gov/pubmed/28732469
http://dx.doi.org/10.1186/s12864-017-3881-5
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author Araya, Susan
Martins, Alexandre M
Junqueira, Nilton T V
Costa, Ana Maria
Faleiro, Fábio G
Ferreira, Márcio E
author_facet Araya, Susan
Martins, Alexandre M
Junqueira, Nilton T V
Costa, Ana Maria
Faleiro, Fábio G
Ferreira, Márcio E
author_sort Araya, Susan
collection PubMed
description BACKGROUND: The Passiflora genus comprises hundreds of wild and cultivated species of passion fruit used for food, industrial, ornamental and medicinal purposes. Efforts to develop genomic tools for genetic analysis of P. edulis, the most important commercial Passiflora species, are still incipient. In spite of many recognized applications of microsatellite markers in genetics and breeding, their availability for passion fruit research remains restricted. Microsatellite markers in P. edulis are usually limited in number, show reduced polymorphism, and are mostly based on compound or imperfect repeats. Furthermore, they are confined to only a few Passiflora species. We describe the use of NGS technology to partially assemble the P. edulis genome in order to develop hundreds of new microsatellite markers. RESULTS: A total of 14.11 Gbp of Illumina paired-end sequence reads were analyzed to detect simple sequence repeat sites in the sour passion fruit genome. A sample of 1300 contigs containing perfect repeat microsatellite sequences was selected for PCR primer development. Panels of di- and tri-nucleotide repeat markers were then tested in P. edulis germplasm accessions for validation. DNA polymorphism was detected in 74% of the markers (PIC = 0.16 to 0.77; number of alleles/locus = 2 to 7). A core panel of highly polymorphic markers (PIC = 0.46 to 0.77) was used to cross-amplify PCR products in 79 species of Passiflora (including P. edulis), belonging to four subgenera (Astrophea, Decaloba, Distephana and Passiflora). Approximately 71% of the marker/species combinations resulted in positive amplicons in all species tested. DNA polymorphism was detected in germplasm accessions of six closely related Passiflora species (P. edulis, P. alata, P. maliformis, P. nitida, P. quadrangularis and P. setacea) and the data used for accession discrimination and species assignment. CONCLUSION: A database of P. edulis DNA sequences obtained by NGS technology was examined to identify microsatellite repeats in the sour passion fruit genome. Markers were submitted to evaluation using accessions of cultivated and wild Passiflora species. The new microsatellite markers detected high levels of DNA polymorphism in sour passion fruit and can potentially be used in genetic analysis of P. edulis and other Passiflora species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3881-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-55203612017-07-21 Microsatellite marker development by partial sequencing of the sour passion fruit genome (Passiflora edulis Sims) Araya, Susan Martins, Alexandre M Junqueira, Nilton T V Costa, Ana Maria Faleiro, Fábio G Ferreira, Márcio E BMC Genomics Research Article BACKGROUND: The Passiflora genus comprises hundreds of wild and cultivated species of passion fruit used for food, industrial, ornamental and medicinal purposes. Efforts to develop genomic tools for genetic analysis of P. edulis, the most important commercial Passiflora species, are still incipient. In spite of many recognized applications of microsatellite markers in genetics and breeding, their availability for passion fruit research remains restricted. Microsatellite markers in P. edulis are usually limited in number, show reduced polymorphism, and are mostly based on compound or imperfect repeats. Furthermore, they are confined to only a few Passiflora species. We describe the use of NGS technology to partially assemble the P. edulis genome in order to develop hundreds of new microsatellite markers. RESULTS: A total of 14.11 Gbp of Illumina paired-end sequence reads were analyzed to detect simple sequence repeat sites in the sour passion fruit genome. A sample of 1300 contigs containing perfect repeat microsatellite sequences was selected for PCR primer development. Panels of di- and tri-nucleotide repeat markers were then tested in P. edulis germplasm accessions for validation. DNA polymorphism was detected in 74% of the markers (PIC = 0.16 to 0.77; number of alleles/locus = 2 to 7). A core panel of highly polymorphic markers (PIC = 0.46 to 0.77) was used to cross-amplify PCR products in 79 species of Passiflora (including P. edulis), belonging to four subgenera (Astrophea, Decaloba, Distephana and Passiflora). Approximately 71% of the marker/species combinations resulted in positive amplicons in all species tested. DNA polymorphism was detected in germplasm accessions of six closely related Passiflora species (P. edulis, P. alata, P. maliformis, P. nitida, P. quadrangularis and P. setacea) and the data used for accession discrimination and species assignment. CONCLUSION: A database of P. edulis DNA sequences obtained by NGS technology was examined to identify microsatellite repeats in the sour passion fruit genome. Markers were submitted to evaluation using accessions of cultivated and wild Passiflora species. The new microsatellite markers detected high levels of DNA polymorphism in sour passion fruit and can potentially be used in genetic analysis of P. edulis and other Passiflora species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3881-5) contains supplementary material, which is available to authorized users. BioMed Central 2017-07-21 /pmc/articles/PMC5520361/ /pubmed/28732469 http://dx.doi.org/10.1186/s12864-017-3881-5 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 Research Article
Araya, Susan
Martins, Alexandre M
Junqueira, Nilton T V
Costa, Ana Maria
Faleiro, Fábio G
Ferreira, Márcio E
Microsatellite marker development by partial sequencing of the sour passion fruit genome (Passiflora edulis Sims)
title Microsatellite marker development by partial sequencing of the sour passion fruit genome (Passiflora edulis Sims)
title_full Microsatellite marker development by partial sequencing of the sour passion fruit genome (Passiflora edulis Sims)
title_fullStr Microsatellite marker development by partial sequencing of the sour passion fruit genome (Passiflora edulis Sims)
title_full_unstemmed Microsatellite marker development by partial sequencing of the sour passion fruit genome (Passiflora edulis Sims)
title_short Microsatellite marker development by partial sequencing of the sour passion fruit genome (Passiflora edulis Sims)
title_sort microsatellite marker development by partial sequencing of the sour passion fruit genome (passiflora edulis sims)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520361/
https://www.ncbi.nlm.nih.gov/pubmed/28732469
http://dx.doi.org/10.1186/s12864-017-3881-5
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