Evidence map›Paper›PMID 29979772›Full record

ArticlePloS one2018

The genome assembly of the fungal pathogen Pyrenochaeta lycopersici from Single-Molecule Real-Time sequencing sheds new light on its biological complexity.

Alessandra Dal Molin, Andrea Minio, Francesca Griggio, Massimo Delledonne, Alessandro Infantino, Maria Aragona

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. 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
1.2field-weighted citation impact, top 24% 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, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Structured Framework and Genome Analysis ofJournal of fungi (Basel, Switzerland) · 2022
    Article
  7. Review
  8. Genome Analysis of the Broad Host Range NecrotrophFrontiers in plant science · 2022
    Article
  9. Review
  10. International journal of molecular sciences · 2021
    Article
  11. Article
  12. Article
  13. 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 2 institutions in 1 country.

Alessandra Dal MolinDipartimento di Biotecnologie, Università degli Studi di Verona, Verona, Italy.ORCID 0000-0001-6281-9589
Andrea MinioDipartimento di Biotecnologie, Università degli Studi di Verona, Verona, Italy.ORCID 0000-0003-2643-9209
Francesca GriggioDipartimento di Biotecnologie, Università degli Studi di Verona, Verona, Italy.
Massimo DelledonneDipartimento di Biotecnologie, Università degli Studi di Verona, Verona, Italy.
Alessandro InfantinoConsiglio per la ricerca in agricoltura e l'analisi dell'economia agraria, Research Centre for Plant Protection and Certification, Rome, Italy.
Maria AragonaConsiglio per la ricerca in agricoltura e l'analisi dell'economia agraria, Research Centre for Plant Protection and Certification, Rome, Italy.ORCID 0000-0002-1320-2141
University of Verona · ITConsiglio per la ricerca in agricoltura e l’analisi dell’economia agraria · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The first draft genome sequencing of the non-model fungal pathogen Pyrenochaeta lycopersici showed an expansion of gene families associated with heterokaryon incompatibility and lacking of mating-type genes, providing insights into the genetic basis of this "imperfect" fungus which lost the ability to produce the sexual stage. However, due to the Illumina short-read technology, the draft genome was too fragmented to allow a comprehensive characterization of the genome, especially of the repetitive sequence fraction. In this work, the sequencing of another P. lycopersici isolate using long-read Single Molecule Real-Time sequencing technology was performed with the aim of obtaining a gapless genome. Indeed, a gapless genome assembly of 62.7 Mb was obtained, with a fraction of repetitive sequences representing 30% of the total bases. The gene content of the two P. lycopersici isolates was very similar, and the large difference in genome size (about 8 Mb) might be attributable to the high fraction of repetitive sequences detected for the new sequenced isolate. The role of repetitive elements, including transposable elements, in modulating virulence effectors is well established in fungal plant pathogens. Moreover, transposable elements are of fundamental importance in creating and re-modelling genes, especially in imperfect fungi. Their abundance in P. lycopersici, together with the large expansion of heterokaryon incompatibility genes in both sequenced isolates, suggest the presence of possible mechanisms alternative to gene re-assorting mediated by sexual recombination. A quite large fraction (~9%) of repetitive elements in P. lycopersici, has no homology with known classes, strengthening this hypothesis. The availability of a gapless genome of P. lycopersici allowed the in-depth analysis of its genome content, by annotating functional genes and TEs. This goal will be an important resource for shedding light on the evolution of the reproductive and pathogenic behaviour of this soilborne pathogen and the onset of a possible speciation within this species.

Indexed as

Genome, FungalAscomycotaChromosome MappingComputer SystemsDNA, FungalDNA Transposable ElementsMolecular Sequence AnnotationPhylogenySequence Analysis, DNADNA, FungalDNA Transposable Elements

Identifiers

PMID29979772
PMCPMC6034849
OpenAlexW2847541658

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.