Evidence map›Paper›PMID 26985669›Full record

ArticlePloS one2016

Natural Genetic Variation Influences Protein Abundances in C. elegans Developmental Signalling Pathways.

Kapil Dev Singh, Bernd Roschitzki, L Basten Snoek, Jonas Grossmann, Xue Zheng, Mark Elvin, Polina Kamkina, Sabine P Schrimpf, Gino B Poulin, Jan E Kammenga and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.6field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
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  7. The GeneG3 (Bethesda, Md.) · 2020
    Article
  8. Article
  9. WormQTL2: an interactive platform for systems genetics in Caenorhabditis elegans.Database : the journal of biological databases and curation · 2020
    Article
  10. Virulence · 2019
    Article
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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

11 authors at 4 institutions in 3 countries.

Kapil Dev SinghInstitute of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.
Bernd RoschitzkiFunctional Genomics Center Zurich, University of Zurich and ETH Zurich, Zurich, Switzerland.
L Basten SnoekLaboratory of Nematology, Wageningen University, Wageningen, The Netherlands.
Jonas GrossmannFunctional Genomics Center Zurich, University of Zurich and ETH Zurich, Zurich, Switzerland.
Xue ZhengInstitute of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.
Mark ElvinFaculty of Life Sciences, The University of Manchester, Manchester, United Kingdom.
Polina KamkinaInstitute of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.
Sabine P SchrimpfInstitute of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.
Gino B PoulinFaculty of Life Sciences, The University of Manchester, Manchester, United Kingdom.
Jan E KammengaLaboratory of Nematology, Wageningen University, Wageningen, The Netherlands.
Michael O HengartnerInstitute of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.
University of Zurich · CHETH Zurich · CHUniversity of Manchester · GBWageningen University & Research · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Complex traits, including common disease-related traits, are affected by many different genes that function in multiple pathways and networks. The apoptosis, MAPK, Notch, and Wnt signalling pathways play important roles in development and disease progression. At the moment we have a poor understanding of how allelic variation affects gene expression in these pathways at the level of translation. Here we report the effect of natural genetic variation on transcript and protein abundance involved in developmental signalling pathways in Caenorhabditis elegans. We used selected reaction monitoring to analyse proteins from the abovementioned four pathways in a set of recombinant inbred lines (RILs) generated from the wild-type strains N2 (Bristol) and CB4856 (Hawaii) to enable quantitative trait locus (QTL) mapping. About half of the cases from the 44 genes tested showed a statistically significant change in protein abundance between various strains, most of these were however very weak (below 1.3-fold change). We detected a distant QTL on the left arm of chromosome II that affected protein abundance of the phosphatidylserine receptor protein PSR-1, and two separate QTLs that influenced embryonic and ionizing radiation-induced apoptosis on chromosome IV. Our results demonstrate that natural variation in C. elegans is sufficient to cause significant changes in signalling pathways both at the gene expression (transcript and protein abundance) and phenotypic levels.

Indexed as

AnimalsApoptosisCaenorhabditis elegansCaenorhabditis elegans ProteinsChromosome MappingGene Expression Regulation, DevelopmentalGenetic VariationQuantitative Trait LociSignal TransductionTranscriptional ActivationCaenorhabditis elegans Proteins

Identifiers

PMID26985669
PMCPMC4795773
OpenAlexW2302275992

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.