Evidence map›Paper›PMID 25683721›Full record

ArticleCell reports2015

Systematic Discovery of Human Gene Function and Principles of Modular Organization through Phylogenetic Profiling.

Gautam Dey, Ariel Jaimovich, Sean R Collins, Akiko Seki, Tobias Meyer

Abstract read
In one paragraph

Article in Cell reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing 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

47 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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  5. Article
  6. C11orf54 catalyzes L-xylulose formation in human metabolism.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Phylogenetic profiling in eukaryotes comes of age.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  16. Identification of hidden associations among eukaryotic genes through statistical analysis of coevolutionary transitions.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  17. Article
  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

5 authors.

Gautam DeyDepartment of Chemical and Systems Biology, Stanford University, Stanford, CA 94305, USA.
Ariel JaimovichDepartment of Chemical and Systems Biology, Stanford University, Stanford, CA 94305, USA.
Sean R CollinsDepartment of Chemical and Systems Biology, Stanford University, Stanford, CA 94305, USA.
Akiko SekiDepartment of Chemical and Systems Biology, Stanford University, Stanford, CA 94305, USA.
Tobias MeyerDepartment of Chemical and Systems Biology, Stanford University, Stanford, CA 94305, USA. Electronic address: tobias1@stanford.edu.

Funding

TRAINING & OUTREACH COREP50GM107615 · NIGMS · STANFORD UNIVERSITY · PI FERRELL, JAMES E. · 2013 to 2017
$10.9M
Chemotactic Signal TransductionR01GM063702 · NIGMS · STANFORD UNIVERSITY · PI MEYER, TOBIAS · 2002 to 2017
$5.3M
REGULATION OF CA++/CALMODULIN KINASE BY NEUROTRANSMITTERR01GM030179 · NIGMS · STANFORD UNIVERSITY · PI MEYER, TOBIAS · 1985 to 2018
$4.9M
REGULATION OF CA++/CALMODULIN KINASE BY NEUROTRANSMITTERR37GM030179 · NIGMS · STANFORD UNIVERSITY · PI MEYER, TOBIAS · 1995 to 2004
$1.7M
NIGMS NIH HHS P50 GM107615NIGMS NIH HHS R01 GM030179NIGMS NIH HHS R01 GM063702NIGMS NIH HHS R37 GM030179
6 · The paper itself

Abstract

Functional links between genes can be predicted using phylogenetic profiling, by correlating the appearance and loss of homologs in subsets of species. However, effective genome-wide phylogenetic profiling has been hindered by the large fraction of human genes related to each other through historical duplication events. Here, we overcame this challenge by automatically profiling over 30,000 groups of homologous human genes (orthogroups) representing the entire protein-coding genome across 177 eukaryotic species (hOP profiles). By generating a full pairwise orthogroup phylogenetic co-occurrence matrix, we derive unbiased genome-wide predictions of functional modules (hOP modules). Our approach predicts functions for hundreds of poorly characterized genes. The results suggest evolutionary constraints that lead components of protein complexes and metabolic pathways to co-evolve while genes in signaling and transcriptional networks do not. As a proof of principle, we validated two subsets of candidates experimentally for their predicted link to the actin-nucleating WASH complex and cilia/basal body function.

Identifiers

PMID25683721
PMCPMC5016211

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Registered trials

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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.