Evidence map›Paper›PMID 26911875›Full record

ArticleBMC genomics2016

Comparative genome analysis and genome evolution of members of the magnaporthaceae family of fungi.

Laura H Okagaki, Joshua K Sailsbery, Alexander W Eyre, Ralph A Dean

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.1field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Comparative Genomics of ThreeFrontiers in microbiology · 2022
    Article
  7. Article
  8. Microorganisms · 2021
    Article
  9. Article
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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

4 authors at 1 institution in 1 country.

Laura H OkagakiCenter for Integrated Fungal Research, North Carolina State University, 851 Main campus Drive, Raleigh, NC, 27606, USA. laura.okagaki@gmail.com.
Joshua K SailsberyCenter for Integrated Fungal Research, North Carolina State University, 851 Main campus Drive, Raleigh, NC, 27606, USA. jsailsbery@hotmail.com.
Alexander W EyreCenter for Integrated Fungal Research, North Carolina State University, 851 Main campus Drive, Raleigh, NC, 27606, USA. aweyre@ncsu.edu.
Ralph A DeanCenter for Integrated Fungal Research, North Carolina State University, 851 Main campus Drive, Raleigh, NC, 27606, USA. radean2@ncsu.edu.
North Carolina State University · US

Funding

Tri-Institutional Molecular Mycology and Pathogenesis Training ProgramT32AI052080 · NIAID · DUKE UNIVERSITY · PI ANDREW ALSPAUGH, JOSEPH HEITMAN · 2003 to 2026
$8.7M
NIAID NIH HHS NIH 5 T32-AI052080-09NIAID NIH HHS T32 AI052080
6 · The paper itself

Abstract

backgroundMagnaporthaceae, a family of ascomycetes, includes three fungi of great economic importance that cause disease in cereal and turf grasses: Magnaporthe oryzae (rice blast), Gaeumannomyces graminis var. tritici (take-all disease), and Magnaporthe poae (summer patch disease). Recently, the sequenced and assembled genomes for these three fungi were reported. Here, the genomes were compared for orthologous genes in order to identified genes that are unique to the Magnaporthaceae family of fungi. In addition, ortholog clustering was used to identify a core proteome for the Magnaporthaceae, which was examined for diversifying and purifying selection and evidence of two-speed genome evolution.

resultsA genome-scale comparative study was conducted across 74 fungal genomes to identify clusters of orthologous genes unique to the three Magnaporthaceae species as well as species specific genes. We found 1149 clusters that were unique to the Magnaporthaceae family of fungi with 295 of those containing genes from all three species. Gene clusters involved in metabolic and enzymatic activities were highly represented in the Magnaporthaceae specific clusters. Also highly represented in the Magnaporthaceae specific clusters as well as in the species specific genes were transcriptional regulators. In addition, we examined the relationship between gene evolution and distance to repetitive elements found in the genome. No correlations between diversifying or purifying selection and distance to repetitive elements or an increased rate of evolution in secreted and small secreted proteins were observed.

conclusionsTaken together, these data show that at the genome level, there is no evidence to suggest multi-speed genome evolution or that proximity to repetitive elements play a role in diversification of genes.

Indexed as

Biological EvolutionGenome, FungalAscomycotaComparative Genomic HybridizationFungal ProteinsMagnaportheMultigene FamilyPhylogenyProteomeSpecies SpecificityTranscription FactorsFungal ProteinsProteomeTranscription Factors

Identifiers

PMID26911875
PMCPMC4766678
OpenAlexW2279493624

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.