Evidence map›Paper›PMID 18077348›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

Reconstruction of ancestral protein interaction networks for the bZIP transcription factors.

John W Pinney, Grigoris D Amoutzias, Magnus Rattray, David L Robertson

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

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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

21 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Bayesian inference for duplication-mutation with complementarity network models.Journal of computational biology : a journal of computational molecular cell biology · 2015
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Parsimonious reconstruction of network evolution.Algorithms for molecular biology : AMB · 2012
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Making the right connections: biological networks in the light of evolution.BioEssays : news and reviews in molecular, cellular and developmental biology · 2009
    Article
  20. Model criticism based on likelihood-free inference, with an application to protein network evolution.Proceedings of the National Academy of Sciences of the United States of America · 2009
    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.

John W PinneyFaculty of Life Sciences and School of Computer Science, University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom. john.pinney@manchester.ac.uk
Grigoris D Amoutzias
Magnus Rattray
David L Robertson

Funding

Biotechnology and Biological Sciences Research Council BB/C515412/1
6 · The paper itself

Abstract

As whole-genome protein-protein interaction datasets become available for a wide range of species, evolutionary biologists have the opportunity to address some of the unanswered questions surrounding the evolution of these complex systems. Protein interaction networks from divergent organisms may be compared to investigate how gene duplication, deletion, and rewiring processes have shaped the evolution of their contemporary structures. However, current approaches for comparing observed networks from multiple species lack the phylogenetic context necessary to reconstruct the evolutionary history of a network. Here we show how probabilistic modeling can provide a platform for the quantitative analysis of multiple protein interaction networks. We apply this technique to the reconstruction of ancestral networks for the bZIP family of transcription factors and find that excellent agreement is obtained with an alternative sequence-based method for the prediction of leucine zipper interactions. Further analysis shows our probabilistic method to be significantly more robust to the presence of noise in the observed network data than a simple parsimony-based approach. In addition, the integration of evidence over multiple species means that the same method may be used to improve the quality of noisy interaction data for extant species. The ancestral states of a protein interaction network have been reconstructed here by using an explicit probabilistic model of network evolution. We anticipate that this model will form the basis of more general methods for probing the evolutionary history of biochemical networks.

Indexed as

Models, StatisticalProtein Interaction MappingAnimalsBasic-Leucine Zipper Transcription FactorsEvolution, MolecularHumansBasic-Leucine Zipper Transcription Factors

Identifiers

PMID18077348
PMCPMC2154451

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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.