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Related Concept Videos

Protein Networks02:26

Protein Networks

An organism can have thousands of different proteins, and these proteins must cooperate to ensure the health of an organism. Proteins bind to other proteins and form complexes to carry out their functions. Many proteins interact with multiple other proteins creating a complex network of protein interactions.
These interactions can be represented through maps depicting protein-protein interaction networks, represented as nodes and edges. Nodes are circles that are representative of a protein,...
Protein Networks02:26

Protein Networks

An organism can have thousands of different proteins, and these proteins must cooperate to ensure the health of an organism. Proteins bind to other proteins and form complexes to carry out their functions. Many proteins interact with multiple other proteins creating a complex network of protein interactions.
These interactions can be represented through maps depicting protein-protein interaction networks, represented as nodes and edges. Nodes are circles that are representative of a protein,...
IP3/DAG Signaling Pathway01:11

IP3/DAG Signaling Pathway

Membrane lipids such as phosphatidylinositol (PI) are precursors for several membrane-bound and soluble second messengers. Specific kinases phosphorylate PI and produce phosphorylated inositol phospholipids. One such inositol phospholipids are the  phosphatidylinositol-4,5 bisphosphate [PI(4,5)P2], present in the inner half of the lipid bilayer. Upon ligand binding, GPCR stimulates Gq proteins to turn on phospholipase Cꞵ. Activated phospholipase Cꞵ cleaves PI(4,5)P2 and produces two-second...
Interactions Between Signaling Pathways01:19

Interactions Between Signaling Pathways

Signaling cascades usually lack linearity. Multiple pathways interact and regulate one another, allowing cells to integrate and respond to diverse environmental stimuli.
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...

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Related Experiment Video

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A Web Tool for Generating High Quality Machine-readable Biological Pathways
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A Web Tool for Generating High Quality Machine-readable Biological Pathways

Published on: February 8, 2017

BN+1 Bayesian network expansion for identifying molecular pathway elements.

Andrew P Hodges1, Peter Woolf, Yongqun He

  • 1Center for Computational Medicine and Bioinformatics; University of Michigan Medical School; University of Michigan; Michigan USA.

Communicative & Integrative Biology
|February 19, 2011
PubMed
Summary
This summary is machine-generated.

The BN+1 algorithm identifies new gene interactions using gene expression data. It found fdhE as a potential regulator in the reactive oxygen species (ROS) pathway, advancing systems biology.

Keywords:
BN+1E. coliROSbayesian networkbiofilmgene interactionmicroarray data analysisnetwork expansionreactive oxygen speciessynthetic network

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Area of Science:

  • Systems Biology
  • Bioinformatics
  • Molecular Biology

Background:

  • Identifying gene interactions is crucial for understanding biological pathways.
  • Existing methods may not capture complex, non-linear gene regulatory relationships.
  • Microarray gene expression data offers a rich source for inferring these interactions.

Purpose of the Study:

  • To evaluate the BN+1 Bayesian network expansion algorithm for identifying undocumented gene interactions.
  • To assess the algorithm's ability to detect both linear and non-linear relationships.
  • To validate the algorithm's performance using both synthetic and experimental data.

Main Methods:

  • Development and application of the Bayesian network expansion algorithm (BN+1).
  • Utilizing microarray gene expression data to infer gene regulatory networks.
  • Design of a synthetic network for algorithm validation.
  • Analysis of experimentally derived data from E. coli.

Main Results:

  • The BN+1 algorithm successfully identified known gene interactions and key regulators like uspE.
  • The method demonstrated proficiency in detecting both linear and non-linear relationships.
  • BN+1 correctly identified variables proximal to the initial network structure.
  • The gene fdhE was identified as a potential novel regulator in the reactive oxygen species (ROS) pathway.

Conclusions:

  • The BN+1 algorithm is effective for discovering novel gene interactions and regulators.
  • The algorithm's ability to handle complex relationships enhances its utility in systems biology.
  • Further refinement of score cutoff criteria is proposed for optimizing BN+1 call selection.