Evidence map›Paper›PMID 37355591›Full record

ArticleBMC ecology and evolution2023

High functional allelic diversity and copy number in both MHC classes in the common buzzard.

Jamie Winternitz, Nayden Chakarov, Tony Rinaud, Meinolf Ottensmann, Oliver Krüger

Open access · goldAbstract read
In one paragraph

Article in BMC ecology and evolution, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Possible Shifts in the Genetic Diversity of Red-crowned Cranes (Animals : an open access journal from MDPI · 2024
    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

5 authors at 1 institution in 1 country.

Jamie WinternitzDepartment of Animal Behaviour, Bielefeld University, Morgenbreede 45, 33615, Bielefeld, Germany. jamie.winternitz@uni-bielefeld.de.ORCID 0000-0002-1113-9126
Nayden ChakarovDepartment of Animal Behaviour, Bielefeld University, Morgenbreede 45, 33615, Bielefeld, Germany.ORCID 0000-0002-9124-1242
Tony RinaudDepartment of Animal Behaviour, Bielefeld University, Morgenbreede 45, 33615, Bielefeld, Germany.ORCID 0000-0003-3811-2270
Meinolf OttensmannDepartment of Animal Behaviour, Bielefeld University, Morgenbreede 45, 33615, Bielefeld, Germany.ORCID 0000-0003-3112-6928
Oliver KrügerDepartment of Animal Behaviour, Bielefeld University, Morgenbreede 45, 33615, Bielefeld, Germany.
Bielefeld University · DE

Funding

Deutsche Forschungsgemeinschaft 316099922Deutsche Forschungsgemeinschaft 398434413Deutsche Forschungsgemeinschaft 433069365
6 · The paper itself

Abstract

backgroundThe major histocompatibility complex (MHC), which encodes molecules that recognize various pathogens and parasites and initiates the adaptive immune response in vertebrates, is renowned for its exceptional polymorphism and is a model of adaptive gene evolution. In birds, the number of MHC genes and sequence diversity varies greatly among taxa, believed due to evolutionary history and differential selection pressures. Earlier characterization studies and recent comparative studies suggest that non-passerine species have relatively few MHC gene copies compared to passerines. Additionally, comparative studies that have looked at partial MHC sequences have speculated that non-passerines have opposite patterns of selection on MHC class I (MHC-I) and class II (MHC-II) loci than passerines: namely, greater sequence diversity and signals of selection on MHC-II than MHC-I. However, new sequencing technology is revealing much greater MHC variation than previously expected while also facilitating full sequence variant detection directly from genomic data. Our study aims to take advantage of high-throughput sequencing methods to fully characterize both classes and domains of MHC of a non-passerine bird of prey, the common buzzard (Buteo buteo), to test predictions of MHC variation and differential selection on MHC classes.

resultsUsing genetic, genomic, and transcriptomic high-throughput sequencing data, we established common buzzards have at least three loci that produce functional alleles at both MHC classes. In total, we characterize 91 alleles from 113 common buzzard chicks for MHC-I exon 3 and 41 alleles from 125 chicks for MHC-IIB exon 2. Among these alleles, we found greater sequence polymorphism and stronger diversifying selection at MHC-IIB exon 2 than MHC-I exon 3, suggesting differential selection pressures on MHC classes. However, upon further investigation of the entire peptide-binding groove by including genomic data from MHC-I exon 2 and MHC-IIA exon 2, this turned out to be false. MHC-I exon 2 was as polymorphic as MHC-IIB exon 2 and MHC-IIA exon 2 was essentially invariant. Thus, comparisons between MHC-I and MHC-II that included both domains of the peptide-binding groove showed no differences in polymorphism nor diversifying selection between the classes. Nevertheless, selection analysis indicates balancing selection has been acting on common buzzard MHC and phylogenetic inference revealed that trans-species polymorphism is present between common buzzards and species separated for over 33 million years for class I and class II.

conclusionsWe characterize and confirm the functionality of unexpectedly high copy number and allelic diversity in both MHC classes of a bird of prey. While balancing selection is acting on both classes, there is no evidence of differential selection pressure on MHC classes in common buzzards and this result may hold more generally once more data for understudied MHC exons becomes available.

Indexed as

DNA Copy Number VariationsMajor Histocompatibility ComplexAllelesAnimalsPeptidesPhylogenyPeptidesBirds of preyButeo buteoCharacterizationCopy number variationGenotypingHigh-throughput sequencingLong-read sequencingMajor histocompatibility complexNonclassical MHCPeptide-binding groovePeptide binding residuesRNAseqSelectionTrans-species polymorphism

Identifiers

PMID37355591
PMCPMC10290333
OpenAlexW4381930618

What OpenQuestion holds

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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.