Evidence map›Paper›PMID 28544882›Full record

ArticleCell systems2017

Inference and Evolutionary Analysis of Genome-Scale Regulatory Networks in Large Phylogenies.

Christopher Koch, Jay Konieczka, Toni Delorey, Ana Lyons, Amanda Socha, Kathleen Davis, Sara A Knaack, Dawn Thompson, Erin K O'Shea, Aviv Regev and 1 more

Abstract read
In one paragraph

Article in Cell systems, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Gene Regulatory Networks ofFrontiers in microbiology · 2020
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Christopher KochDepartment of Computer Sciences, University of Wisconsin-Madison, Madison, WI 53706, USA.
Jay KonieczkaBroad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Toni DeloreyBroad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Ana LyonsDepartment of Biology, Massachusetts Institute of Technology, Cambridge, MA 02142, USA.
Amanda SochaDartmouth College, Biology Department, Hanover, NH 03755, USA.
Kathleen DavisDepartment of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA.
Sara A KnaackWisconsin Institute for Discovery, 330 North Orchard Street, Madison, WI 53715, USA.
Dawn ThompsonBroad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Erin K O'SheaDepartment of Chemistry and Chemical Biology, Harvard University, Cambridge, MA 02138, USA; Howard Hughes Medical Institute, Harvard University, Northwest Laboratory, Cambridge, MA 02138, USA; Faculty of Arts and Sciences Center for Systems Biology, Harvard University, Northwest Laboratory, Cambridge, MA 02138, USA; Department of Molecular and Cellular Biology, Harvard University, Northwest Laboratory, Cambridge, MA 02138, USA.
Aviv RegevBroad Institute of MIT and Harvard, Cambridge, MA 02142, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA.
Sushmita RoyWisconsin Institute for Discovery, 330 North Orchard Street, Madison, WI 53715, USA; Department of Biostatistics and Medical Informatics, University of Wisconsin-Madison, Madison, WI 53792, USA. Electronic address: sroy@biostat.wisc.edu.

Funding

Research Training for Computation and Informatics in Biology and MedicineT15LM007359 · NLM · UNIVERSITY OF WISCONSIN-MADISON · PI Mark W. Craven, Colin Noel Dewey · 2002 to 2026
$22.6M
Genome-wide analysis of regulated chromosomal domains: From mechanisms to cancerR01CA119176 · NCI · WEIZMANN INSTITUTE OF SCIENCE · PI REGEV, AVIV, SEGAL, ERAN · 2006 to 2015
$3.7M
The temporal reconfiguration of regulatory networks: From yeast to cancerDP1OD003958 · OD · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI REGEV, AVIV · 2008 to 2011
$3.3M
Howard Hughes Medical InstituteNCI NIH HHS R01 CA119176NIH HHS DP1 OD003958NLM NIH HHS T15 LM007359Wellcome Trust
6 · The paper itself

Abstract

Changes in transcriptional regulatory networks can significantly contribute to species evolution and adaptation. However, identification of genome-scale regulatory networks is an open challenge, especially in non-model organisms. Here, we introduce multi-species regulatory network learning (MRTLE), a computational approach that uses phylogenetic structure, sequence-specific motifs, and transcriptomic data, to infer the regulatory networks in different species. Using simulated data from known networks and transcriptomic data from six divergent yeasts, we demonstrate that MRTLE predicts networks with greater accuracy than existing methods because it incorporates phylogenetic information. We used MRTLE to infer the structure of the transcriptional networks that control the osmotic stress responses of divergent, non-model yeast species and then validated our predictions experimentally. Interrogating these networks reveals that gene duplication promotes network divergence across evolution. Taken together, our approach facilitates study of regulatory network evolutionary dynamics across multiple poorly studied species.

Indexed as

AlgorithmsBiological EvolutionComputational BiologyComputer SimulationEvolution, MolecularGene Expression ProfilingGene Regulatory NetworksGenomeModels, GeneticPhylogenyStress, PhysiologicalTranscriptomeYeastscomparative functional genomicsevolution of gene regulatory networksevolution of stress responsenetwork inferencephylogenyprobabilistic graphical modelregulatory networksyeast

Identifiers

PMID28544882
PMCPMC5515301

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.