Evidence map›Paper›PMID 18398455›Full record

ArticlePloS one2008

Mapping genetically compensatory pathways from synthetic lethal interactions in yeast.

Xiaotu Ma, Aaron M Tarone, Wenyuan Li

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 7% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Yeast Sphingolipid Phospholipase GeneMolecular and cellular biology · 2020
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Systems genetics in "-omics" era: current and future development.Theory in biosciences = Theorie in den Biowissenschaften · 2013
    Review
  15. Article
  16. Article
  17. Review
  18. Inferring mechanisms of compensation from E-MAP and SGA data using local search algorithms for max cut.Journal of computational biology : a journal of computational molecular cell biology · 2011
    Article
  19. Discovering novel subsystems using comparative genomics.Bioinformatics (Oxford, England) · 2011
    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

3 authors at 1 institution in 1 country.

Xiaotu MaMolecular and Computational Biology Program, Department of Biological Sciences, University of Southern California, Los Angeles, California, United States of America. xma@usc.edu
Aaron M Tarone
Wenyuan Li
University of Southern California · US

Funding

Implications of haplotype structure in the human genomeP50HG002790 · NHGRI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TAVARE, SIMON · 2003 to 2013
$29.9M
NHGRI NIH HHS P50 HG 002790NHGRI NIH HHS P50 HG002790
6 · The paper itself

Abstract

backgroundSynthetic lethal genetic interaction analysis has been successfully applied to predicting the functions of genes and their pathway identities. In the context of synthetic lethal interaction data alone, the global similarity of synthetic lethal interaction patterns between two genes is used to predict gene function. With physical interaction data, such as protein-protein interactions, the enrichment of physical interactions within subsets of genes and the enrichment of synthetic lethal interactions between those subsets of genes are used as an indication of compensatory pathways.

resultIn this paper, we propose a method of mapping genetically compensatory pathways from synthetic lethal interactions. Our method is designed to discover pairs of gene-sets in which synthetic lethal interactions are depleted among the genes in an individual set and where such gene-set pairs are connected by many synthetic lethal interactions. By its nature, our method could select compensatory pathway pairs that buffer the deleterious effect of the failure of either one, without the need of physical interaction data. By focusing on compensatory pathway pairs where genes in each individual pathway have a highly homogenous cellular function, we show that many cellular functions have genetically compensatory properties.

conclusionWe conclude that synthetic lethal interaction data are a powerful source to map genetically compensatory pathways, especially in systems lacking physical interaction information, and that the cellular function network contains abundant compensatory properties.

Indexed as

Gene Expression Regulation, FungalAlgorithmsComputational BiologyDatabases, ProteinGenes, FungalGenetic TechniquesGenome, FungalGolgi ApparatusMicrotubule-Associated ProteinsModels, GeneticModels, StatisticalProtein Interaction MappingSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsYeastsMicrotubule-Associated ProteinsSaccharomyces cerevisiae Proteins

Identifiers

PMID18398455
PMCPMC2275788
OpenAlexW2039366890

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.