Evidence map›Paper›PMID 32998693›Full record

ArticleBMC genomics2020

Genetic diversity, evolution and selection in the major histocompatibility complex DRB and DQB loci in the family Equidae.

Marie Klumplerova, Petra Splichalova, Jan Oppelt, Jan Futas, Aneta Kohutova, Petra Musilova, Svatava Kubickova, Roman Vodicka, Ludovic Orlando, Petr Horin

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

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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

10 authors at 4 institutions in 3 countries.

Marie KlumplerovaDepartment of Animal Genetics, Veterinary and Pharmaceutical University, Brno, Czech Republic.
Petra SplichalovaDepartment of Animal Genetics, Veterinary and Pharmaceutical University, Brno, Czech Republic.
Jan OppeltCeitec VFU, RG Animal Immunogenomics, Brno, Czech Republic.
Jan FutasDepartment of Animal Genetics, Veterinary and Pharmaceutical University, Brno, Czech Republic.
Aneta KohutovaDepartment of Animal Genetics, Veterinary and Pharmaceutical University, Brno, Czech Republic.
Petra MusilovaDepartment of Genetics and Reproductive Biotechnologies, Veterinary Research Institute, Brno, Czech Republic.
Svatava KubickovaDepartment of Genetics and Reproductive Biotechnologies, Veterinary Research Institute, Brno, Czech Republic.
Roman VodickaZoo Prague, U Trojského zámku 120/3, 171 00, Praha 7, Czech Republic.
Ludovic OrlandoLaboratoire d'Anthropobiologie Moléculaire et d'Imagerie de Synthèse, CNRS UMR 5288, Université de Toulouse, Université Paul Sabatier, 31000, Toulouse, France.
Petr HorinDepartment of Animal Genetics, Veterinary and Pharmaceutical University, Brno, Czech Republic. horin@dior.ics.muni.cz.ORCID http://orcid.org/0000-0002-5548-4212
University of Veterinary Sciences Brno · CZCentral European Institute of Technology · CZCentre National de la Recherche Scientifique · FRPrague Zoo · CZ

Funding

Central European Institute of Technology CEITEC CZ.1.05/1.1.00/02.0068Czech National Sustainability Programme NPU LQ1601
6 · The paper itself

Abstract

backgroundThe mammalian Major Histocompatibility Complex (MHC) is a genetic region containing highly polymorphic genes with immunological functions. MHC class I and class II genes encode antigen-presenting molecules expressed on the cell surface. The MHC class II sub-region contains genes expressed in antigen presenting cells. The antigen binding site is encoded by the second exon of genes encoding antigen presenting molecules. The exon 2 sequences of these MHC genes have evolved under the selective pressure of pathogens. Interspecific differences can be observed in the class II sub-region. The family Equidae includes a variety of domesticated, and free-ranging species inhabiting a range of habitats exposed to different pathogens and represents a model for studying this important part of the immunogenome. While equine MHC class II DRA and DQA loci have received attention, the genetic diversity and effects of selection on DRB and DQB loci have been largely overlooked. This study aimed to provide the first in-depth analysis of the MHC class II DRB and DQB loci in the Equidae family.

resultsThree DRB and two DQB genes were identified in the genomes of all equids. The genes DRB2, DRB3 and DQB3 showed high sequence conservation, while polymorphisms were more frequent at DRB1 and DQB1 across all species analyzed. DQB2 was not found in the genome of the Asiatic asses Equus hemionus kulan and E. h. onager. The bioinformatic analysis of non-zero-coverage-bases of DRB and DQB genes in 14 equine individual genomes revealed differences among individual genes. Evidence for recombination was found for DRB1, DRB2, DQB1 and DQB2 genes. Trans-species allele sharing was identified in all genes except DRB1. Site-specific selection analysis predicted genes evolving under positive selection both at DRB and DQB loci. No selected amino acid sites were identified in DQB3.

conclusionsThe organization of the MHC class II sub-region of equids is similar across all species of the family. Genomic sequences, along with phylogenetic trees suggesting effects of selection as well as trans-species polymorphism support the contention that pathogen-driven positive selection has shaped the MHC class II DRB/DQB sub-regions in the Equidae.

Indexed as

Evolution, MolecularPolymorphism, GeneticSelection, GeneticAnimalsEquidaeGenetic SpeciationMajor Histocompatibility ComplexPhylogenyRecombination, GeneticFamily EquidaeMajor histocompatibility complexMHC class II lociMHC exon 2Positive selectionSelected amino acid sitesTrans-species polymorphism

Identifiers

PMID32998693
PMCPMC7525986
OpenAlexW3090532133

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.