Evidence map›Paper›PMID 22823938›Full record

ArticleBMC genomics2012

A survey of putative secreted and transmembrane proteins encoded in the C. elegans genome.

Jinkyo Suh, Harald Hutter

Abstract read
In one paragraph

Article in BMC genomics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

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

26 citing papers in PubMed.

  1. Article
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  10. Pathways that affect anterior morphogenesis inbioRxiv : the preprint server for biology · 2023
    Article
  11. Article
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  14. Article
  15. Review
  16. Article
  17. Article
  18. The R148.3 Gene ModulatesG3 (Bethesda, Md.) · 2017
    Article
  19. Article
  20. 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

2 authors.

Jinkyo SuhDepartment of Biological Sciences, Simon Fraser University, Burnaby, BC, Canada.
Harald Hutter

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

backgroundAlmost half of the Caenorhabditis elegans genome encodes proteins with either a signal peptide or a transmembrane domain. Therefore a substantial fraction of the proteins are localized to membranes, reside in the secretory pathway or are secreted. While these proteins are of interest to a variety of different researchers ranging from developmental biologists to immunologists, most of secreted proteins have not been functionally characterized so far.

resultsWe grouped proteins containing a signal peptide or a transmembrane domain using various criteria including evolutionary origin, common domain organization and functional categories. We found that putative secreted proteins are enriched for small proteins and nematode-specific proteins. Many secreted proteins are predominantly expressed in specific life stages or in one of the two sexes suggesting stage- or sex-specific functions. More than a third of the putative secreted proteins are upregulated upon exposure to pathogens, indicating that a substantial fraction may have a role in immune response. Slightly more than half of the transmembrane proteins can be grouped into broad functional categories based on sequence similarity to proteins with known function. By far the largest groups are channels and transporters, various classes of enzymes and putative receptors with signaling function.

conclusionOur analysis provides an overview of all putative secreted and transmembrane proteins in C. elegans. This can serve as a basis for selecting groups of proteins for large-scale functional analysis using reverse genetic approaches.

Indexed as

Gene ExpressionAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsFemaleGenetic Association StudiesGenome, HelminthMaleMembrane ProteinsProtein Sorting SignalsProtein Structure, TertiarySex FactorsSignal TransductionTime FactorsCaenorhabditis elegans ProteinsMembrane ProteinsProtein Sorting Signals

Identifiers

PMID22823938
PMCPMC3534327

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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.