Abstract

Biological systems are exquisitely poised to respond and adjust to challenges, including damage. However, sustained damage can overcome the ability of the system to adjust and result in a disease phenotype, its underpinnings many times elusive. Unraveling the molecular mechanisms of systems biology, of how and why it falters, is essential for delineating the details of the path(s) leading to the diseased state and for designing strategies to revert its progression. An important aspect of this process is not only to define the function of a gene but to identify the context within which gene functions act. It is within the network, or pathway context, that the function of a gene fulfills its ultimate biological role. Resolving the extent to which defective function(s) affect the proceedings of pathway(s) and how altered pathways merge into overpowering the system's defense machinery are key to understanding the molecular aspects of disease and envisioning ways to counteract it. A network-centric approach to diseases is increasingly being considered in current research. It also underlies the deployment of disease pathways at the Rat Genome Database Pathway Portal. The portal is presented with an emphasis on disease and altered pathways, associated drug pathways, pathway suites, and suite networks. The Pathway Portal at the Rat Genome Database (RGD) provides an ever-increasing collection of interactive pathway diagrams and associated annotations for metabolic, signaling, regulatory, and drug pathways, including disease and altered pathways. A disease pathway is viewed from the perspective of networks whose alterations are manifested in the affected phenotype. The Pathway Ontology (PW), built and maintained at RGD, facilitates the annotations of genes, the deployment of pathway diagrams, and provides an overall navigational tool. Pathways that revolve around a common concept and are globally connected are presented within pathway suites; a suite network combines two or more pathway suites. The Pathway Portal is a rich resource that offers a range of pathway data and visualization, including disease pathways and related pathway suites. Viewing a disease pathway from the perspective of underlying altered pathways is an aid for dissecting the molecular mechanisms of disease.

Highlights

  • Biological systems are exquisitely poised to respond and adjust to challenges, including damage

  • A stands for annotations, D stands for diagrams, and the light versus dark shade(s) distinguish between annotations and/or diagrams to children or to term(s), respectively

  • The Rat Genome Database (RGD) Pathway Portal houses an ever-increasing collection of interactive diagram pages for metabolic, regulatory, signaling, drug, and disease and associated altered pathways along with related pathway suites and suite networks for those pathways that globally revolve around a common concept

Read more

Summary

Introduction

Biological systems are exquisitely poised to respond and adjust to challenges, including damage. While the physical boundaries of such units are in many instances fluid, their delineation by the research community establishes a paradigm for studying the working of biomolecules within a context These can be the sets of reactions and interactions that underlie the transformation of compounds, those that are initiated or triggered by a signaling event, or those that aim to maintain the normal status quo of cells and tissue. As available at the sites, were mapped to PW terms as synonyms, and the genes associated with them were matched to RGD rat, human, or mouse genes using the Entrez gene ID and symbol [1] These two pipelines are no longer running as PID has since retired and KEGG has changed its license; the annotations, as last brought in, are still available. A plus sign in front of a term designates the presence of children for that term

Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.