Evidence map›Paper›PMID 28732469›Full record

ArticleBMC genomics2017

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

Susan Araya, Alexandre M Martins, Nilton T V Junqueira, Ana Maria Costa, Fábio G Faleiro, Márcio E Ferreira

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
9.1field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
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  4. Genome-Wide Identification and Characterization of theInternational journal of molecular sciences · 2022
    Article
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  10. Identification of passion fruit (Passiflora edulis) chromosomes using BAC-FISH.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2019
    Article
  11. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Susan ArayaDepartment of Agronomy, Campus Universitário Darcy Ribeiro, University of Brasilia (UnB), Brasília, 70910-900, Brazil.
Alexandre M MartinsEmbrapa Genetic Resources and Biotechnology, Genetics Laboratory, CEP 70770-917, Brasilia, DF, Brazil.
Nilton T V JunqueiraEmbrapa Cerrados, Caixa Postal 08233, CEP, Planaltina, DF, 73310-970, Brazil.
Ana Maria CostaEmbrapa Cerrados, Caixa Postal 08233, CEP, Planaltina, DF, 73310-970, Brazil.
Fábio G FaleiroEmbrapa Cerrados, Caixa Postal 08233, CEP, Planaltina, DF, 73310-970, Brazil.
Márcio E FerreiraEmbrapa Genetic Resources and Biotechnology, Genetics Laboratory, CEP 70770-917, Brasilia, DF, Brazil. marcio.ferreira@embrapa.br.
Brazilian Agricultural Research Corporation · BRAgricultural Research Service · USUniversidade de Brasília · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe 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.

resultsA 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.

conclusionA 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.

Indexed as

GenomicsSequence AnalysisGenome, PlantHigh-Throughput Nucleotide SequencingMicrosatellite RepeatsPassifloraSpecies SpecificityCross-species transferabilityDe novo genome assemblyMicrosatellite

Identifiers

PMID28732469
PMCPMC5520361
OpenAlexW2738920936

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.