Evidence map›Paper›PMID 32525943›Full record

ArticlePloS one2020

Chromosome evolution in Lophyohylini (Amphibia, Anura, Hylinae).

Pablo Suárez, Juan M Ferro, Cleusa Y Nagamachi, Dario E Cardozo, Ailin Blasco-Zúñiga, Jéssica B Silva, Euvaldo Marciano-Jr, Marco A Costa, Victor G D Orrico, Mirco Solé and 6 more

Abstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

16 authors.

Pablo SuárezInstituto de Biología Subtropical (CONICET-UNaM), Puerto Iguazú, Misiones, Argentina.
Juan M FerroLaboratorio de Genética Evolutiva "Claudio J. Bidau", Instituto de Biología Subtropical (CONICET-UNaM), Facultad de Ciencias Exactas, Químicas y Naturales, Universidad Nacional de Misiones, Posadas, Misiones, Argentina.ORCID 0000-0003-0287-5567
Cleusa Y NagamachiLaboratório de Citogenética, Centro de Estudos Avançados da Biodiversidade, Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém, Pará, Brasil.
Dario E CardozoLaboratorio de Genética Evolutiva "Claudio J. Bidau", Instituto de Biología Subtropical (CONICET-UNaM), Facultad de Ciencias Exactas, Químicas y Naturales, Universidad Nacional de Misiones, Posadas, Misiones, Argentina.ORCID 0000-0003-0612-2458
Ailin Blasco-ZúñigaLaboratorio de Investigación de Citogenética y Biomoléculas de Anfibios (LICBA), Centro de Investigación para la Salud en América Latina-CISeAL, Facultad de Ciencias Exactas y Naturales, Pontificia Universidad Católica del Ecuador, Quito, Ecuador.ORCID 0000-0002-7318-2795
Jéssica B SilvaLaboratório de Citogenética, Centro de Estudos Avançados da Biodiversidade, Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém, Pará, Brasil.
Euvaldo Marciano-JrDepartamento de Ciências Biológicas, Universidade Estadual de Santa Cruz, Ilhéus, Bahia, Brazil.ORCID 0000-0002-7647-2480
Marco A CostaDepartamento de Ciências Biológicas, Universidade Estadual de Santa Cruz, Ilhéus, Bahia, Brazil.
Victor G D OrricoDepartamento de Ciências Biológicas, Universidade Estadual de Santa Cruz, Ilhéus, Bahia, Brazil.ORCID 0000-0002-4560-4006
Mirco SoléDepartamento de Ciências Biológicas, Universidade Estadual de Santa Cruz, Ilhéus, Bahia, Brazil.ORCID 0000-0001-7881-6227
Igor J RobertoDepartamento de Ciências Biológicas, Pós-graduação em Zoologia, Universidade Federal do Amazonas, Amazonas, Brazil.ORCID 0000-0003-3268-9597
Miryan RiveraLaboratorio de Investigación de Citogenética y Biomoléculas de Anfibios (LICBA), Centro de Investigación para la Salud en América Latina-CISeAL, Facultad de Ciencias Exactas y Naturales, Pontificia Universidad Católica del Ecuador, Quito, Ecuador.
John E WileyDepartment of Pediatrics/Medical Genetics, East Carolina University School of Medicine, Greenville, NC, United States of America.
Julián FaivovichDivisión Herpetología, Museo Argentino de Ciencias Naturales "Bernardino Rivadavia"-CONICET, Buenos Aires, Argentina.
Diego BaldoLaboratorio de Genética Evolutiva "Claudio J. Bidau", Instituto de Biología Subtropical (CONICET-UNaM), Facultad de Ciencias Exactas, Químicas y Naturales, Universidad Nacional de Misiones, Posadas, Misiones, Argentina.ORCID 0000-0003-2382-0872
Julio C PieczarkaLaboratório de Citogenética, Centro de Estudos Avançados da Biodiversidade, Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém, Pará, Brasil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The hyline tribe Lophyohylini includes 87 species of treefrogs, of which cytogenetics aspects have been studied in less than 20% of them. In order to evaluate the evolution of some of its chromosome characters (NOR position, C-bands, and DAPI/CMA3 bands), we studied the karyotypes of 21 lophyohylines, 16 of them for the first time, and analyzed them in a phylogenetic context. Most species showed similar karyotypes regarding chromosome number (2n = 24) and morphology (FN = 48), excepting Phyllodytes edelmoi and Osteocephalus buckleyi with 2n = 22 (FN = 44) and 2n = 28 (FN = 50), respectively. The NOR location was variable among species and provided valuable phylogenetic information. This marker was located in pair 11 in all species of Trachycephalus, Itapotihyla langsdorffii, and Nyctimantis arapapa, representing the plesiomorphic condition of Lophyohylini. Besides, other apomorphic states were recovered for the clades comprising N. rugiceps and N. siemersi (NOR in pair 5), and Dryaderces pearsoni, Osteocephalus, and Osteopilus (NOR in pair 9). Phyllodytes presented variation for NORs position; they were in pair 2 in P. edelmoi, pair 7 in P. melanomystax, and pair 8 in P. gyrinaethes and P. praeceptor. Polymorphisms in size, number, and activity of this marker were observed for N. siemersi, Osteocephalus fuscifacies, and some species of Trachycephalus. Remarkably, in N. siemersi NORs were detected on a single chromosome in the two specimens studied by this technique, raising the question of how this complex polymorphism is maintained. Interstitial telomeric sequences were found in P. edelmoi, P. melanomystax, and Osteocephalus buckleyi, and their presence seems to be not related to the chromosome reorganization events. Finally, some species showed spontaneous rearrangements, possibly as a consequence of an uncommon phenomenon in anuran cytogenetics: the presence of fragile sites or secondary constrictions not associated with NORs. We propose that this rare feature would have played an important role in the evolution of this group of frogs. From the evidence obtained in this and previous studies, we conclude that Lophyohylini presents a complex chromosome evolution.

Indexed as

AnimalsAnuraChromosome BandingChromosome Fragile SitesChromosomesCytogenetic AnalysisEvolution, MolecularFemaleKaryotypeMaleNucleolus Organizer RegionPhylogenyPolymorphism, GeneticSouth AmericaSpecies SpecificityTelomere

Identifiers

PMID32525943
PMCPMC7289402

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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.