Evidence map›Paper›PMID 28851275›Full record

ArticleBMC genomics2017

Gapless genome assembly of Colletotrichum higginsianum reveals chromosome structure and association of transposable elements with secondary metabolite gene clusters.

Jean-Félix Dallery, Nicolas Lapalu, Antonios Zampounis, Sandrine Pigné, Isabelle Luyten, Joëlle Amselem, Alexander H J Wittenberg, Shiguo Zhou, Marisa V de Queiroz, Guillaume P Robin and 9 more

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 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
24.8field-weighted citation impact, top 1% 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

55 citing papers in PubMed, 119 citations in OpenAlex.

  1. Chromosome-Level Genome Assembly and Annotation of theJournal of fungi (Basel, Switzerland) · 2026
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  8. Comparative Genomic Analyses ofJournal of fungi (Basel, Switzerland) · 2024
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  10. The Molecular Genetics and Genomics of Plant-Pathogen Interactions.International journal of molecular sciences · 2024
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  12. Genome Comparisons betweenJournal of fungi (Basel, Switzerland) · 2024
    Article
  13. Comparative Genomic Analysis ofJournal of fungi (Basel, Switzerland) · 2023
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Chromosome-level analysis of theFrontiers in microbiology · 2023
    Article
  20. Review
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

19 authors at 10 institutions in 7 countries.

Jean-Félix DalleryUMR BIOGER, INRA, AgroParisTech, Université Paris-Saclay, Thiverval-Grignon, France.
Nicolas LapaluUMR BIOGER, INRA, AgroParisTech, Université Paris-Saclay, Thiverval-Grignon, France.
Antonios ZampounisUMR BIOGER, INRA, AgroParisTech, Université Paris-Saclay, Thiverval-Grignon, France.
Sandrine PignéUMR BIOGER, INRA, AgroParisTech, Université Paris-Saclay, Thiverval-Grignon, France.
Isabelle LuytenUR1164 URGI, INRA, Versailles, France.
Joëlle AmselemUR1164 URGI, INRA, Versailles, France.
Alexander H J WittenbergKeyGene N.V., Wageningen, The Netherlands.
Shiguo ZhouLaboratory for Molecular and Computational Genomics, Department of Chemistry, Laboratory of Genetics, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Marisa V de QueirozLaboratório de Genética Molecular de Fungos, Universidade Federal de Viçosa, Viçosa, Brazil.
Guillaume P RobinUMR BIOGER, INRA, AgroParisTech, Université Paris-Saclay, Thiverval-Grignon, France.
Annie AugerUMR BIOGER, INRA, AgroParisTech, Université Paris-Saclay, Thiverval-Grignon, France.
Matthieu HainautCNRS UMR 7257, Aix-Marseille University, Marseille, France.
Bernard HenrissatCNRS UMR 7257, Aix-Marseille University, Marseille, France.
Ki-Tae KimDepartment of Agricultural Biotechnology, Center for Fungal Genetic Resources, Seoul National University, Seoul, Korea.
Yong-Hwan LeeDepartment of Agricultural Biotechnology, Center for Fungal Genetic Resources, Seoul National University, Seoul, Korea.
Olivier LespinetLaboratoire de Recherche en Informatique, CNRS, Université Paris-Sud, Orsay, France.
David C SchwartzLaboratory for Molecular and Computational Genomics, Department of Chemistry, Laboratory of Genetics, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Michael R ThonInstituto Hispano-Luso de Investigaciones Agrarias (CIALE), Department of Microbiology and Genetics, University of Salamanca, Salamanca, Spain.
Richard J O'ConnellUMR BIOGER, INRA, AgroParisTech, Université Paris-Saclay, Thiverval-Grignon, France. richard.oconnell@inra.fr.
Biologie et Gestion des Risques en Agriculture · FRCentre National de la Recherche Scientifique · FRSeoul National University · KRUniversity of Wisconsin–Madison · USAgroParisTech · FRKeyGene (Netherlands) · NLLaboratoire de Recherche en Informatique · FRUniversidad de Salamanca · ESUniversidade Federal de Viçosa · BRUniversité Paris-Saclay · FR

Funding

NEW PHYSICAL METHODOLOGIES FOR GENOMIC ANALYSISR01HG000225 · NHGRI · UNIVERSITY OF WISCONSIN-MADISON · PI SCHWARTZ, DAVID C. · 1991 to 2014
$5.2M
NHGRI NIH HHS R01 HG000225
6 · The paper itself

Abstract

backgroundThe ascomycete fungus Colletotrichum higginsianum causes anthracnose disease of brassica crops and the model plant Arabidopsis thaliana. Previous versions of the genome sequence were highly fragmented, causing errors in the prediction of protein-coding genes and preventing the analysis of repetitive sequences and genome architecture.

resultsHere, we re-sequenced the genome using single-molecule real-time (SMRT) sequencing technology and, in combination with optical map data, this provided a gapless assembly of all twelve chromosomes except for the ribosomal DNA repeat cluster on chromosome 7. The more accurate gene annotation made possible by this new assembly revealed a large repertoire of secondary metabolism (SM) key genes (89) and putative biosynthetic pathways (77 SM gene clusters). The two mini-chromosomes differed from the ten core chromosomes in being repeat- and AT-rich and gene-poor but were significantly enriched with genes encoding putative secreted effector proteins. Transposable elements (TEs) were found to occupy 7% of the genome by length. Certain TE families showed a statistically significant association with effector genes and SM cluster genes and were transcriptionally active at particular stages of fungal development. All 24 subtelomeres were found to contain one of three highly-conserved repeat elements which, by providing sites for homologous recombination, were probably instrumental in four segmental duplications.

conclusionThe gapless genome of C. higginsianum provides access to repeat-rich regions that were previously poorly assembled, notably the mini-chromosomes and subtelomeres, and allowed prediction of the complete SM gene repertoire. It also provides insights into the potential role of TEs in gene and genome evolution and host adaptation in this asexual pathogen.

Indexed as

GenomicsChromosomes, FungalColletotrichumDNA Transposable ElementsHomologous RecombinationMolecular Sequence AnnotationMultigene FamilyPhylogenyPoint MutationDNA Transposable Elementsaccessory chromosomesColletotrichum higginsianumFungal genomeoptical mapsecondary metabolism genessegmental duplicationSMRT sequencingsubtelomerestransposable elements

Identifiers

PMID28851275
PMCPMC5576322
OpenAlexW2752683716

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.