Evidence map›Paper›PMID 27261006›Full record

ArticleG3 (Bethesda, Md.)2016

Characterization of a Single Genomic Locus Encoding the Clustered Protocadherin Receptor Diversity in Xenopus tropicalis.

Hakki E Etlioglu, Wei Sun, Zengjin Huang, Wei Chen, Dietmar Schmucker

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 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
–field-weighted citation impact
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

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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.

  1. Article
  2. Review
  3. Protocadherins at the Crossroad of Signaling Pathways.Frontiers in molecular neuroscience · 2020
    Review
  4. Frontiers in physiology · 2018
    Article
  5. Regulation of neural circuit formation by protocadherins.Cellular and molecular life sciences : CMLS · 2017
    Review
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.

Hakki E EtliogluNeuronal Wiring Laboratory, Vlaams Instituut voor Biotechnologie (VIB), University of Leuven, 3000, Belgium Department of Human Genetics, School of Medicine, University of Leuven, 3000 Belgium.
Wei SunLaboratory for Functional Genomics and Systems Biology, Berlin Institute for Medical Systems Biology, Max-Delbrück-Centrum für Molekulare Medizin, 13125 Berlin, Germany.
Zengjin HuangNeuronal Wiring Laboratory, Vlaams Instituut voor Biotechnologie (VIB), University of Leuven, 3000, Belgium Department of Human Genetics, School of Medicine, University of Leuven, 3000 Belgium.
Wei ChenLaboratory for Functional Genomics and Systems Biology, Berlin Institute for Medical Systems Biology, Max-Delbrück-Centrum für Molekulare Medizin, 13125 Berlin, Germany wei.chen@mdc-berlin.de dietmar.schmucker@vib-kuleuven.be.
Dietmar SchmuckerNeuronal Wiring Laboratory, Vlaams Instituut voor Biotechnologie (VIB), University of Leuven, 3000, Belgium Department of Human Genetics, School of Medicine, University of Leuven, 3000 Belgium wei.chen@mdc-berlin.de dietmar.schmucker@vib-kuleuven.be.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clustered protocadherins (cPcdhs) constitute the largest subgroup of the cadherin superfamily, and in mammals are grouped into clusters of α-, β-, and γ-types. Tens of tandemly arranged paralogous Pcdh genes of the Pcdh clusters generate a substantial diversity of receptor isoforms. cPcdhs are known to have important roles in neuronal development, and genetic alterations of cPcdhs have been found to be associated with several neurological diseases. Here, we present a first characterization of cPcdhs in Xenopus tropicalis We determined and annotated all cPcdh isoforms, revealing that they are present in a single chromosomal locus. We validated a total of 96 isoforms, which we show are organized in three distinct clusters. The X. tropicalis cPcdh locus is composed of one α- and two distinct γ-Pcdh clusters (pcdh-γ1 and pcdh-γ2). Bioinformatics analyses assisted by genomic BAC clone sequencing showed that the X. tropicalis α- and γ-Pcdhs are conserved at the cluster level, but, unlike mammals, X. tropicalis does not contain a β-Pcdh cluster. In contrast, the number of γ-Pcdh isoforms has expanded, possibly due to lineage-specific gene duplications. Interestingly, the number of X. tropicalis α-Pcdhs is identical between X. tropicalis and mouse. Moreover, we find highly conserved as well as novel promoter elements potentially involved in regulating the cluster-specific expression of cPcdh isoforms. This study provides important information for the understanding of the evolutionary history of cPcdh genes and future mechanistic studies. It provides an annotated X. tropicalis cPcdh genomic map and a first molecular characterization essential for functional and comparative studies.

Indexed as

Genetic VariationGenomicsAnimalsBrainCadherinsCell DifferentiationHumansMiceMultigene FamilyProtein IsoformsXenopusCadherinsProtein Isoformsgene clusterneuronal developmentprotocadherin receptor diversityXenopus tropicalis

Identifiers

PMID27261006
PMCPMC4978886

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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.