Evidence map›Paper›PMID 27517292›Full record

ArticleImmunogenetics2017

Egernia stokesii (gidgee skink) MHC I positively selected sites lack concordance with HLA peptide binding regions.

Sarah K Pearson, C Michael Bull, Michael G Gardner

Abstract read
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In one paragraph

Article in Immunogenetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

1 citing paper in PubMed, 8 citations in OpenAlex.

  1. 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

3 authors at 2 institutions in 1 country.

Sarah K PearsonSchool of Biological Sciences, Flinders University of South Australia, Bedford Park, Adelaide, 5042, Australia. sarah.pearson@flinders.edu.au.
C Michael BullSchool of Biological Sciences, Flinders University of South Australia, Bedford Park, Adelaide, 5042, Australia.
Michael G GardnerSchool of Biological Sciences, Flinders University of South Australia, Bedford Park, Adelaide, 5042, Australia.
Flinders University · AUSouth Australian Museum · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genes of the major histocompatibility complex (MHC) play an important role in vertebrate disease resistance, kin recognition and mate choice. Mammalian MHC is the most widely characterised of all vertebrates, and attention is often given to the peptide binding regions of the MHC because they are presumed to be under stronger selection than non-peptide binding regions. For vertebrates where the MHC is less well understood, researchers commonly use the amino acid positions of the peptide binding regions of the human leukocyte antigen (HLA) to infer the peptide binding regions within the MHC sequences of their taxon of interest. However, positively selected sites within MHC have been reported to lack correspondence with the HLA in fish, frogs, birds and reptiles including squamates. Despite squamate diversity, the MHC has been characterised in few snakes and lizards. The Egernia group of scincid lizards is appropriate for investigating mechanisms generating MHC variation, as their inclusion will add a new lineage (i.e. Scincidae) to studies of selection on the MHC. We aimed to identify positively selected sites within the MHC of Egernia stokesii and then determine if these sites corresponded with the peptide binding regions of the HLA. Six positively selected sites were identified within E. stokesii MHC I, only two were homologous with the HLA. E. stokesii positively selected sites corresponded more closely to non-lizard than other lizard taxa. The characterisation of the MHC of more intermediate taxa within the squamate order is necessary to understand the evolution of the MHC across all vertebrates.

Indexed as

Biological EvolutionAllelesAmino Acid SequenceAnimalsHistocompatibility Antigens Class IHLA AntigensHumansLizardsPeptide FragmentsProtein BindingSequence Homology, Amino AcidHistocompatibility Antigens Class IHLA AntigensPeptide FragmentsEgernia stokesiiMHCPeptide binding regionPositively selected sitesScincidaeSquamata

Identifiers

PMID27517292
OpenAlexW2508483767

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.