Evidence map›Paper›PMID 18463698›Full record

ArticlePLoS computational biology2008

Systematic analysis of pleiotropy in C. elegans early embryogenesis.

Lihua Zou, Sira Sriswasdi, Brian Ross, Patrycja V Missiuro, Jun Liu, Hui Ge

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

18 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Computational and structural biotechnology journal · 2025
    Article
  4. Article
  5. Article
  6. Transcriptome Analysis of Maternal Gene Transcripts in Unfertilized Eggs ofInternational journal of molecular sciences · 2020
    Article
  7. Why does allometry evolve so slowly?Integrative and comparative biology · 2019
    Article
  8. Article
  9. Article
  10. Body maps on the human genome.Molecular cytogenetics · 2013
    Article
  11. The many faces of pleiotropy.Trends in genetics : TIG · 2013
    Article
  12. Aquatic models, genomics and chemical risk management.Comparative biochemistry and physiology. Toxicology & pharmacology : CBP · 2012
    Article
  13. Article
  14. Article
  15. Whole-animal imaging, gene function, and the Zebrafish Phenome Project.Current opinion in genetics & development · 2011
    Review
  16. Article
  17. Information flow analysis of interactome networks.PLoS computational biology · 2009
    Article
  18. 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

6 authors at 2 institutions in 1 country.

Lihua ZouDepartment of Statistics, Harvard University, Cambridge, Massachusetts, USA.
Sira Sriswasdi
Brian Ross
Patrycja V Missiuro
Jun Liu
Hui Ge
Whitehead Institute for Biomedical Research · USHarvard University · US

Funding

Systems Biology of Sporulation in Bacillus SubtilisR01GM078990 · NIGMS · HARVARD UNIVERSITY · PI LIU, JUN S · 2006 to 2009
$1.3M
NIGMS NIH HHS R01 GM078990NIGMS NIH HHS R01-GM078990
6 · The paper itself

Abstract

Pleiotropy refers to the phenomenon in which a single gene controls several distinct, and seemingly unrelated, phenotypic effects. We use C. elegans early embryogenesis as a model to conduct systematic studies of pleiotropy. We analyze high-throughput RNA interference (RNAi) data from C. elegans and identify "phenotypic signatures", which are sets of cellular defects indicative of certain biological functions. By matching phenotypic profiles to our identified signatures, we assign genes with complex phenotypic profiles to multiple functional classes. Overall, we observe that pleiotropy occurs extensively among genes involved in early embryogenesis, and a small proportion of these genes are highly pleiotropic. We hypothesize that genes involved in early embryogenesis are organized into partially overlapping functional modules, and that pleiotropic genes represent "connectors" between these modules. In support of this hypothesis, we find that highly pleiotropic genes tend to reside in central positions in protein-protein interaction networks, suggesting that pleiotropic genes act as connecting points between different protein complexes or pathways.

Indexed as

Models, BiologicalAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCell CycleCell Cycle ProteinsComputer SimulationEmbryonic DevelopmentEvolution, MolecularGene Expression ProfilingMutationPhenotypeSignal TransductionCaenorhabditis elegans ProteinsCell Cycle Proteins

Identifiers

PMID18463698
PMCPMC2265476
OpenAlexW2102807476

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.