Evidence map›Paper›PMID 28100699›Full record

ArticleNucleic acids research2017

Proteogenomics produces comprehensive and highly accurate protein-coding gene annotation in a complete genome assembly of Malassezia sympodialis.

Yafeng Zhu, Pär G Engström, Christian Tellgren-Roth, Charles D Baudo, John C Kennell, Sheng Sun, R Blake Billmyre, Markus S Schröder, Anna Andersson, Tina Holm and 12 more

Abstract read
In one paragraph

Article in Nucleic acids research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Frequent transitions in mating-type locus chromosomal organization inProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  6. Frequent transitions in mating-type locus chromosomal organization inbioRxiv : the preprint server for biology · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Identification ofFrontiers in cellular and infection microbiology · 2020
    Article
  15. Approaches for Genetic Discoveries in the Skin Commensal and PathogenicFrontiers in cellular and infection microbiology · 2020
    Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

22 authors.

Yafeng ZhuScience for Life Laboratory, Department of Oncology-Pathology, Karolinska Institutet, 17121 Solna, Sweden.
Pär G EngströmScience for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, 17121 Solna, Sweden.
Christian Tellgren-RothNational Genomics Infrastructure, Science for Life Laboratory, Department of Immunology, Genetics and Pathology, Uppsala University, 75108 Uppsala, Sweden.
Charles D BaudoDepartment of Biology, Saint Louis University, St. Louis, MO 63103, USA.
John C KennellDepartment of Biology, Saint Louis University, St. Louis, MO 63103, USA.
Sheng SunDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
R Blake BillmyreDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Markus S SchröderSchool of Biomedical and Biomolecular Science, Conway Institute, University College Dublin, Belfield, Dublin 4, Ireland.
Anna AnderssonDepartment of Medicine Solna, Translational Immunology Unit, Karolinska Institutet and University Hospital, 17177 Stockholm, Sweden.
Tina HolmDepartment of Medicine Solna, Translational Immunology Unit, Karolinska Institutet and University Hospital, 17177 Stockholm, Sweden.
Benjamin SigurgeirssonScience for Life Laboratory, School of Biotechnology, Royal Institute of Technology, 17121 Solna, Sweden.
Guangxi WuComputational and Systems Biology, Genome Institute of Singapore, Agency for Science, Technology and Research (A*STAR), 138672, Singapore.
Sundar Ram SankaranarayananMolecular Mycology Laboratory, Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur, Bangalore 560 064, India.
Rahul SiddharthanThe Institute of Mathematical Sciences/HBNI, Taramani, Chennai 600 113, India.
Kaustuv SanyalMolecular Mycology Laboratory, Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur, Bangalore 560 064, India.
Joakim LundebergScience for Life Laboratory, School of Biotechnology, Royal Institute of Technology, 17121 Solna, Sweden.
Björn NystedtScience for Life Laboratory, Department of Cell and Molecular Biology, Uppsala University, 75123 Uppsala, Sweden.
Teun BoekhoutCBS-Fungal Biodiversity Centre, Utrecht, 3508, The Netherlands and Institute for Biodiversity and ecosystem Dynamics (IBED), University of Amsterdam, 1012 WX Amsterdam, The Netherlands.
Thomas L DawsonInstitute of Medical Biology, Agency for Science, Technology and Research (A*STAR), 138648, Singapore.
Joseph HeitmanDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Annika ScheyniusScience for Life Laboratory, Department of Clinical Science and Education, Karolinska Institutet, and Sachs' Children and Youth Hospital, Södersjukhuset, SE-118 83 Stockholm, Sweden.
Janne LehtiöScience for Life Laboratory, Department of Oncology-Pathology, Karolinska Institutet, 17121 Solna, Sweden.

Funding

ORGANIZATION AND FUNCTIONS OF CELLULAR STRUCTUREST32GM007184 · NIGMS · DUKE UNIVERSITY · PI JINKS-ROBERTSON, SUE · 1985 to 2019
$18.2M
Structure, function, and evolution of the Cryptococcus MAT locusR01AI050113 · NIAID · DUKE UNIVERSITY · PI HEITMAN, JOSEPH · 2002 to 2024
$8.5M
Genetics of Cryptococcus sexual reproductionR37AI039115 · NIAID · DUKE UNIVERSITY · PI HEITMAN, JOSEPH · 2011 to 2020
$4.9M
NIAID NIH HHS R01 AI050113NIAID NIH HHS R37 AI039115NIGMS NIH HHS T32 GM007184
6 · The paper itself

Abstract

Complete and accurate genome assembly and annotation is a crucial foundation for comparative and functional genomics. Despite this, few complete eukaryotic genomes are available, and genome annotation remains a major challenge. Here, we present a complete genome assembly of the skin commensal yeast Malassezia sympodialis and demonstrate how proteogenomics can substantially improve gene annotation. Through long-read DNA sequencing, we obtained a gap-free genome assembly for M. sympodialis (ATCC 42132), comprising eight nuclear and one mitochondrial chromosome. We also sequenced and assembled four M. sympodialis clinical isolates, and showed their value for understanding Malassezia reproduction by confirming four alternative allele combinations at the two mating-type loci. Importantly, we demonstrated how proteomics data could be readily integrated with transcriptomics data in standard annotation tools. This increased the number of annotated protein-coding genes by 14% (from 3612 to 4113), compared to using transcriptomics evidence alone. Manual curation further increased the number of protein-coding genes by 9% (to 4493). All of these genes have RNA-seq evidence and 87% were confirmed by proteomics. The M. sympodialis genome assembly and annotation presented here is at a quality yet achieved only for a few eukaryotic organisms, and constitutes an important reference for future host-microbe interaction studies.

Indexed as

Genome, FungalFungal ProteinsGenes, FungalGenome, MitochondrialMalasseziaMolecular Sequence AnnotationPeptidesProtein DomainsProteogenomicsSequence Analysis, RNAFungal ProteinsPeptides

Identifiers

PMID28100699
PMCPMC5389616

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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.