Evidence map›Paper›PMID 27493218›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Alternative haplotypes of antigen processing genes in zebrafish diverged early in vertebrate evolution.

Sean C McConnell, Kyle M Hernandez, Dustin J Wcisel, Ross N Kettleborough, Derek L Stemple, Jeffrey A Yoder, Jorge Andrade, Jill L O de Jong

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

37 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Antigen Presentation and Autophagy in Teleost Adaptive Immunity.International journal of molecular sciences · 2022
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  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

8 authors at 3 institutions in 2 countries.

Sean C McConnellSection of Hematology-Oncology and Stem Cell Transplant, Department of Pediatrics, The University of Chicago, Chicago, IL 60637; scmcconnell@uchicago.edu jdejong@peds.bsd.uchicago.edu.
Kyle M HernandezCenter for Research Informatics, The University of Chicago, Chicago, IL 60637;
Dustin J WciselDepartment of Molecular Biomedical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, NC 27607; Genomic Sciences Graduate Program, North Carolina State University, Raleigh, NC 27607;
Ross N KettleboroughVertebrate Development and Genetics, Wellcome Trust Sanger Institute, Cambridge CB10 1SA, United Kingdom;
Derek L StempleVertebrate Development and Genetics, Wellcome Trust Sanger Institute, Cambridge CB10 1SA, United Kingdom;
Jeffrey A YoderDepartment of Molecular Biomedical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, NC 27607; Genomic Sciences Graduate Program, North Carolina State University, Raleigh, NC 27607; Comparative Medicine Institute, North Carolina State University, Raleigh, NC 27607.ORCID 0000-0002-6083-1311
Jorge AndradeCenter for Research Informatics, The University of Chicago, Chicago, IL 60637;
Jill L O de JongSection of Hematology-Oncology and Stem Cell Transplant, Department of Pediatrics, The University of Chicago, Chicago, IL 60637; scmcconnell@uchicago.edu jdejong@peds.bsd.uchicago.edu.
University of Chicago · USNorth Carolina State University · USWellcome Sanger Institute · GB

Funding

VIRAL ONCOLOGY CORE FACILITYP30CA014599 · NCI · UNIVERSITY OF CHICAGO · PI CHIEN-MIN KAO · 1985 to 2026
$122.1M
NCI NIH HHS P30 CA014599
6 · The paper itself

Abstract

Antigen processing and presentation genes found within the MHC are among the most highly polymorphic genes of vertebrate genomes, providing populations with diverse immune responses to a wide array of pathogens. Here, we describe transcriptome, exome, and whole-genome sequencing of clonal zebrafish, uncovering the most extensive diversity within the antigen processing and presentation genes of any species yet examined. Our CG2 clonal zebrafish assembly provides genomic context within a remarkably divergent haplotype of the core MHC region on chromosome 19 for six expressed genes not found in the zebrafish reference genome: mhc1uga, proteasome-β 9b (psmb9b), psmb8f, and previously unknown genes psmb13b, tap2d, and tap2e We identify ancient lineages for Psmb13 within a proteasome branch previously thought to be monomorphic and provide evidence of substantial lineage diversity within each of three major trifurcations of catalytic-type proteasome subunits in vertebrates: Psmb5/Psmb8/Psmb11, Psmb6/Psmb9/Psmb12, and Psmb7/Psmb10/Psmb13. Strikingly, nearby tap2 and MHC class I genes also retain ancient sequence lineages, indicating that alternative lineages may have been preserved throughout the entire MHC pathway since early diversification of the adaptive immune system ∼500 Mya. Furthermore, polymorphisms within the three MHC pathway steps (antigen cleavage, transport, and presentation) are each predicted to alter peptide specificity. Lastly, comparative analysis shows that antigen processing gene diversity is far more extensive than previously realized (with ancient coelacanth psmb8 lineages, shark psmb13, and tap2t and psmb10 outside the teleost MHC), implying distinct immune functions and conserved roles in shaping MHC pathway evolution throughout vertebrates.

Indexed as

Biological EvolutionGenomeHaplotypesAnimalsAntigen PresentationCloning, OrganismCysteine EndopeptidasesHigh-Throughput Nucleotide SequencingHistocompatibility Antigens Class IPhylogenyProteasome Endopeptidase ComplexProtein IsoformsTranscriptomeZebrafishZebrafish ProteinsCysteine EndopeptidasesHistocompatibility Antigens Class IProteasome Endopeptidase ComplexProtein IsoformsPsmb7 protein, zebrafishZebrafish ProteinsCG2 clonal zebrafishcomparative genomicsmajor histocompatibilityMHC class I pathwayproteasome and TAP evolution

Identifiers

PMID27493218
PMCPMC5003237
OpenAlexW2482639080

What OpenQuestion holds

Textmetadata
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.