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Related Concept Videos

Covalently Linked Protein Regulators02:04

Covalently Linked Protein Regulators

Proteins can undergo many types of post-translational modifications, often in response to changes in their environment. These modifications play an important role in the function and stability of these proteins. Covalently linked molecules include functional groups, such as methyl, acetyl, and phosphate groups, and also small proteins, such as ubiquitin. There are around 200 different types of covalent regulators that have been identified.
These groups modify specific amino acids in a protein.
Covalently Linked Protein Regulators02:04

Covalently Linked Protein Regulators

Proteins can undergo many types of post-translational modifications, often in response to changes in their environment. These modifications play an important role in the function and stability of these proteins. Covalently linked molecules include functional groups, such as methyl, acetyl, and phosphate groups, and also small proteins, such as ubiquitin. There are around 200 different types of covalent regulators that have been identified.
These groups modify specific amino acids in 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...
Global Regulatory Systems01:28

Global Regulatory Systems

Global regulatory systems in bacteria enable rapid and coordinated responses to environmental changes by integrating sensory inputs with gene expression, ensuring efficient adaptation to fluctuating conditions. Key global regulatory mechanisms include regulons, two-component systems, sigma factors, and secondary messengers.Regulons and Global RegulatorsA regulon is a collection of genes and operons controlled by a common global regulator. These regulators enable bacteria to prioritize resource...
Positive Regulator Molecules02:39

Positive Regulator Molecules

Mitotic cell division results in daughter cells that exactly resemble the parent cell. However, errors in the DNA replication or distribution of genetic material may lead to genetic mutations that may be passed down to every new cell formed from the resulting abnormal cell. Propagation of such mutant cells is restricted through checkpoint mechanisms present at different stages of the cell cycle. These checkpoints involve regulator molecules that either promote or demote cell cycle events.
Positive Regulator Molecules01:45

Positive Regulator Molecules

To consistently produce healthy cells, the cell cycle—the process that generates daughter cells—must be precisely regulated.

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Related Experiment Video

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Using SCOPE to Identify Potential Regulatory Motifs in Coregulated Genes
07:55

Using SCOPE to Identify Potential Regulatory Motifs in Coregulated Genes

Published on: May 31, 2011

Detection of deregulated modules using deregulatory linked path.

Yuxuan Hu1, Lin Gao, Kai Shi

  • 1School of Computer Science and Technology, Xidian University, Xi'an, Shaanxi, China.

Plos One
|July 30, 2013
PubMed
Summary

This study introduces a novel regulatory path-based approach to identify deregulated gene modules by focusing on pathway links, not just individual genes. The method effectively detects condition-specific core regulatory paths (CCRPs) and their associated deregulated modules, aiding in understanding complex diseases.

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Area of Science:

  • Systems Biology
  • Computational Biology
  • Genomics

Background:

  • Identifying deregulated gene modules is crucial for understanding complex diseases, often driven by oncogenes.
  • Existing methods primarily focus on gene deregulation, overlooking the importance of regulatory pathway links.

Purpose of the Study:

  • To develop a novel regulatory path-based approach for detecting deregulated modules by emphasizing deregulated links.
  • To identify condition-specific core regulatory paths (CCRPs) for detecting significant deregulation in regulatory links.

Main Methods:

  • Utilized time-series gene expression data to define regulatory strength between gene pairs via statistical dependence analysis.
  • Applied the shortest path algorithm to identify CCRPs within regulatory networks.
  • Integrated differential edges from CCRPs between case and control groups to derive deregulated modules.

Main Results:

  • The developed method was applied to Human Epidermal Growth Factor Receptor 2 (HER2) expression data.
  • Genes and links within identified deregulated modules showed significant enrichment in KEGG pathways and GO biological processes, validating their relevance.
  • Discovered a significantly deregulated regulatory mechanism involving SNAI1 due to HER2 activation.

Conclusions:

  • The approach provides a strategy for detecting deregulated links in regulatory networks and identifying significant deregulated modules.
  • This contributes to a better understanding of pathogenic processes and aids in the selection of targets for edgetic drugs.