Evidence map›Paper›PMID 31906844›Full record

ArticleBMC evolutionary biology2020

Characterizing the ribosomal tandem repeat and its utility as a DNA barcode in lichen-forming fungi.

Michael Bradshaw, Felix Grewe, Anne Thomas, Cody H Harrison, Hanna Lindgren, Lucia Muggia, Larry L St Clair, H Thorsten Lumbsch, Steven D Leavitt

Open access · goldAbstract read
In one paragraph

Article in BMC evolutionary biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
6.3field-weighted citation impact, top 4% 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

9 citing papers in PubMed, 24 citations in OpenAlex.

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  6. Fungal systematics and evolution · 2021
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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

9 authors at 3 institutions in 2 countries.

Michael BradshawDepartment of Biology, Brigham Young University, 4102 Life Science Building, Provo, UT, 84602, USA.
Felix GreweGrainger Bioinformatics Center, The Field Museum, Chicago, IL, USA.
Anne ThomasDepartment of Biology, Brigham Young University, 4102 Life Science Building, Provo, UT, 84602, USA.
Cody H HarrisonDepartment of Biology, Brigham Young University, 4102 Life Science Building, Provo, UT, 84602, USA.
Hanna LindgrenScience & Education, The Field Museum, Chicago, IL, USA.
Lucia MuggiaDepartment of Life Sciences, University of Trieste, via Giorgieri 10, 34127, Trieste, Italy.
Larry L St ClairDepartment of Biology, Brigham Young University, 4102 Life Science Building, Provo, UT, 84602, USA.
H Thorsten LumbschScience & Education, The Field Museum, Chicago, IL, USA.
Steven D LeavittDepartment of Biology, Brigham Young University, 4102 Life Science Building, Provo, UT, 84602, USA. steve_leavitt@byu.edu.ORCID 0000-0002-5034-9724
Brigham Young University · USField Museum of Natural History · USUniversity of Trieste · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRegions within the nuclear ribosomal operon are a major tool for inferring evolutionary relationships and investigating diversity in fungi. In spite of the prevalent use of ribosomal markers in fungal research, central features of nuclear ribosomal DNA (nrDNA) evolution are poorly characterized for fungi in general, including lichenized fungi. The internal transcribed spacer (ITS) region of the nrDNA has been adopted as the primary DNA barcode identification marker for fungi. However, little is known about intragenomic variation in the nrDNA in symbiotic fungi. In order to better understand evolution of nrDNA and the utility of the ITS region for barcode identification of lichen-forming fungal species, we generated nearly complete nuclear ribosomal operon sequences from nine species in the Rhizoplaca melanophthalma species complex using short reads from high-throughput sequencing.

resultsWe estimated copy numbers for the nrDNA operon, ranging from nine to 48 copies for members of this complex, and found low levels of intragenomic variation in the standard barcode region (ITS). Monophyly of currently described species in this complex was supported in phylogenetic inferences based on the ITS, 28S, intergenic spacer region, and some intronic regions, independently; however, a phylogenetic inference based on the 18S provided much lower resolution. Phylogenetic analysis of concatenated ITS and intergenic spacer sequence data generated from 496 specimens collected worldwide revealed previously unrecognized lineages in the nrDNA phylogeny.

conclusionsThe results from our study support the general assumption that the ITS region of the nrDNA is an effective barcoding marker for fungi. For the R. melanophthalma group, the limited amount of potential intragenomic variability in the ITS region did not correspond to fixed diagnostic nucleotide position characters separating taxa within this species complex. Previously unrecognized lineages inferred from ITS sequence data may represent undescribed species-level lineages or reflect uncharacterized aspects of nrDNA evolution in the R. melanophthalma species complex.

Indexed as

DNA Barcoding, TaxonomicAscomycotaCell NucleusDNA, FungalDNA, IntergenicDNA, RibosomalDNA, Ribosomal SpacerHigh-Throughput Nucleotide SequencingLichensPhylogenySymbiosisTandem Repeat SequencesDNA, FungalDNA, IntergenicDNA, RibosomalDNA, Ribosomal SpacerCopy number variationDNA barcodingITSLichensRepeat regionRhizoplaca

Identifiers

PMID31906844
PMCPMC6945747
OpenAlexW3014007170

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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.