Evidence map›Paper›PMID 27628321›Full record

ArticleOpen biology2016

Different modes of variation for each BG lineage suggest different functions.

John Chattaway, R Andrei Ramirez-Valdez, Paul E Chappell, Joseph J E Caesar, Susan M Lea, Jim Kaufman

Open access · goldAbstract read
In one paragraph

Article in Open biology, 2016. 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
0.5field-weighted citation impact, top 33% 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, 6 citations in OpenAlex.

  1. Review
  2. Fourth Report on Chicken Genes and Chromosomes 2022.Cytogenetic and genome research · 2022
    Review
  3. Review
  4. Article
  5. 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

6 authors at 2 institutions in 1 country.

John ChattawayDepartment of Pathology, University of Cambridge, Cambridge CB2 1QP, UK.
R Andrei Ramirez-ValdezDepartment of Pathology, University of Cambridge, Cambridge CB2 1QP, UK.
Paul E ChappellSir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, UK.
Joseph J E CaesarSir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, UK.
Susan M LeaSir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, UK.
Jim KaufmanDepartment of Pathology, University of Cambridge, Cambridge CB2 1QP, UK Department of Veterinary Medicine, University of Cambridge, Cambridge CB3 0ES, UK jfk31@cam.ac.uk.ORCID 0000-0002-7216-8422
University of Cambridge · GBUniversity of Oxford · GB

Funding

Biotechnology and Biological Sciences Research CouncilWellcome Trust 089305Wellcome Trust RG49834
6 · The paper itself

Abstract

Mammalian butyrophilins have various important functions, one for lipid binding but others as ligands for co-inhibition of αβ T cells or for stimulation of γδ T cells in the immune system. The chicken BG homologues are dimers, with extracellular immunoglobulin variable (V) domains joined by cysteines in the loop equivalent to complementarity-determining region 1 (CDR1). BG genes are found in three genomic locations: BG0 on chromosome 2, BG1 in the classical MHC (the BF-BL region) and many BG genes in the BG region just outside the MHC. Here, we show that BG0 is virtually monomorphic, suggesting housekeeping function(s) consonant with the ubiquitous tissue distribution. BG1 has allelic polymorphism but minimal sequence diversity, with the few polymorphic residues at the interface of the two V domains, suggesting that BG1 is recognized by receptors in a conserved fashion. Any phenotypic variation should be due to the intracellular region, with differential exon usage between alleles. BG genes in the BG region can generate diversity by exchange of sequence cassettes located in loops equivalent to CDR1 and CDR2, consonant with recognition of many ligands or antigens for immune defence. Unlike the mammalian butyrophilins, there are at least three modes by which BG genes evolve.

Indexed as

Genetic VariationAllelesAlternative SplicingAmino Acid SequenceAnimalsAvian ProteinsBase SequenceButyrophilinsChickensChromosomesDNA, ComplementaryEvolution, MolecularExonsModels, ChemicalMyelin-Oligodendrocyte GlycoproteinRNAAvian ProteinsButyrophilinsDNA, ComplementaryMyelin-Oligodendrocyte GlycoproteinRNAavianB-Ggene conversionsegmental exchangeselectionSKINT

Identifiers

PMID27628321
PMCPMC5043582
OpenAlexW2518892559

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.