Evidence map›Paper›PMID 16816419›Full record

ArticleGenetics2006

A genomewide screen for suppressors of par-2 uncovers potential regulators of PAR protein-dependent cell polarity in Caenorhabditis elegans.

Jean-Claude Labbé, Anne Pacquelet, Thomas Marty, Monica Gotta

Abstract read
In one paragraph

Article in Genetics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. De novo mutation inProceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  9. Article
  10. Regulation of Cell Polarity by PAR-1/MARK Kinase.Current topics in developmental biology · 2017
    Review
  11. Mechanisms of polarity protein expression control.Current opinion in cell biology · 2016
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. The PAR network: redundancy and robustness in a symmetry-breaking system.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2013
    Review
  18. 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

4 authors.

Jean-Claude LabbéInstitute of Biochemistry, ETH Zürich, 8093 Zürich, Switzerland.
Anne Pacquelet
Thomas Marty
Monica Gotta

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The PAR proteins play an essential role in establishing and maintaining cell polarity. While their function is conserved across species, little is known about their regulators and effectors. Here we report the identification of 13 potential components of the C. elegans PAR polarity pathway, identified in an RNAi-based, systematic screen to find suppressors of par-2(it5ts) lethality. Most of these genes are conserved in other species. Phenotypic analysis of double-mutant animals revealed that some of the suppressors can suppress lethality associated with the strong loss-of-function allele par-2(lw32), indicating that they might impinge on the PAR pathway independently of the PAR-2 protein. One of these is the gene nos-3, which encodes a homolog of Drosophila Nanos. We find that nos-3 suppresses most of the phenotypes associated with loss of par-2 function, including early cell division defects and maternal-effect sterility. Strikingly, while PAR-1 activity was essential in nos-3; par-2 double mutants, its asymmetric localization at the posterior cortex was not restored, suggesting that the function of PAR-1 is independent of its cortical localization. Taken together, our results identify conserved components that regulate PAR protein function and also suggest a role for NOS-3 in PAR protein-dependent cell polarity.

Indexed as

Genes, SuppressorAnimalsAnimals, Genetically ModifiedBody PatterningCaenorhabditis elegansCaenorhabditis elegans ProteinsCell PolarityChromosome MappingDisorders of Sex DevelopmentEmbryo, NonmammalianFemaleGene Expression Regulation, DevelopmentalGenes, LethalMaleProtein Serine-Threonine KinasesRNA-Binding ProteinsCaenorhabditis elegans Proteinsfem-3-binding protein, C elegansNos-3 protein, C elegansPAR-1 protein, C eleganspar-2 protein, C elegansProtein Serine-Threonine KinasesRNA-Binding ProteinsRNA, Small Interfering

Identifiers

PMID16816419
PMCPMC1569778

What OpenQuestion holds

Textmetadata
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.