Evidence map›Paper›PMID 23072335›Full record

ArticleBMC genetics2012

Gene number determination and genetic polymorphism of the gamma delta T cell co-receptor WC1 genes.

Chuang Chen, Carolyn T A Herzig, Leeson J Alexander, John W Keele, Tara G McDaneld, Janice C Telfer, Cynthia L Baldwin

Open access · diamondAbstract read
In one paragraph

Article in BMC genetics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 29 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

7 authors at 3 institutions in 1 country.

Chuang ChenDepartment of Veterinary and Animal Sciences, University of Massachusetts, Amherst, MA 01003, USA.
Carolyn T A Herzig
Leeson J Alexander
John W Keele
Tara G McDaneld
Janice C Telfer
Cynthia L Baldwin
University of Massachusetts Amherst · USRoman L. Hruska U.S. Meat Animal Research Center · USFort Keogh Livestock and Range Research Laboratory · US

Funding

NICHD NIH HHS R01 HD070056-01
6 · The paper itself

Abstract

backgroundWC1 co-receptors belong to the scavenger receptor cysteine-rich (SRCR) superfamily and are encoded by a multi-gene family. Expression of particular WC1 genes defines functional subpopulations of WC1(+) γδ T cells. We have previously identified partial or complete genomic sequences for thirteen different WC1 genes through annotation of the bovine genome Btau_3.1 build. We also identified two WC1 cDNA sequences from other cattle that did not correspond to sequences in the Btau_3.1 build. Their absence in the Btau_3.1 build may have reflected gaps in the genome assembly or polymorphisms among animals. Since the response of γδ T cells to bacterial challenge is determined by WC1 gene expression, it was critical to understand whether individual cattle or breeds differ in the number of WC1 genes or display polymorphisms.

resultsReal-time quantitative PCR using DNA from the animal whose genome was sequenced ("Dominette") and sixteen other animals representing ten breeds of cattle, showed that the number of genes coding for WC1 co-receptors is thirteen. The complete coding sequences of those thirteen WC1 genes is presented, including the correction of an error in the WC1-2 gene due to mis-assembly in the Btau_3.1 build. All other cDNA sequences were found to agree with the previous annotation of complete or partial WC1 genes. PCR amplification and sequencing of the most variable N-terminal SRCR domain (domain 1 which has the SRCR "a" pattern) of each of the thirteen WC1 genes showed that the sequences are highly conserved among individuals and breeds. Of 160 sequences of domain 1 from three breeds of cattle, no additional sequences beyond the thirteen described WC1 genes were found. Analysis of the complete WC1 cDNA sequences indicated that the thirteen WC1 genes code for three distinct WC1 molecular forms.

conclusionThe bovine WC1 multi-gene family is composed of thirteen genes coding for three structural forms whose sequences are highly conserved among individual cattle and breeds. The sequence diversity necessary for WC1 genes to function as a multi-genic pattern recognition receptor array is encoded in the genome, rather than generated by recombinatorial diversity or hypermutation.

Indexed as

Gene DosagePolymorphism, GeneticAnimalsBase SequenceCattleDatabases, GeneticDNA, ComplementaryGenomeMembrane GlycoproteinsMolecular Sequence DataMultigene FamilyPhylogenyProtein Structure, TertiaryReal-Time Polymerase Chain ReactionReceptors, Antigen, T-Cell, gamma-deltaDMBT1 protein, Bos taurusDNA, ComplementaryMembrane GlycoproteinsReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID23072335
PMCPMC3511184
OpenAlexW2171405006

What OpenQuestion holds

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LicenceCC BY
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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.