Abstract

Transcription factors control which information in a genome becomes transcribed to produce RNAs that function in the biological systems of cells and organisms. Reliable and comprehensive information about transcription factors is invaluable for large-scale network-based studies. However, existing transcription factor knowledge bases are still lacking in well-documented functional information.Here, we provide guidelines for a curation strategy, which constitutes a robust framework for using the controlled vocabularies defined by the Gene Ontology Consortium to annotate specific DNA binding transcription factors (DbTFs) based on experimental evidence reported in literature. Our standardized protocol and workflow for annotating specific DNA binding RNA polymerase II transcription factors is designed to document high-quality and decisive evidence from valid experimental methods. Within a collaborative biocuration effort involving the user community, we are now in the process of exhaustively annotating the full repertoire of human, mouse and rat proteins that qualify as DbTFs in as much as they are experimentally documented in the biomedical literature today. The completion of this task will significantly enrich Gene Ontology-based information resources for the research community.Database URL: www.tfcheckpoint.org

Highlights

  • Specific gene regulation mechanisms determine which part of the genome becomes transcribed to provide the active molecular parts of living organisms in various environmental conditions

  • We provide a detailed report in the form of a comprehensive curation protocol, based on which we are currently engaged in a focused effort to curate all experimentally characterized DNA binding transcription factors (DbTFs) from a collection of candidate proteins compiled from the major TF information sources

  • Sequence-specific DNA binding RNAP II transcription factor activity. The goal of this curation project is to assign a sequence-specific DbTF activity term, i.e. Gene Ontology (GO):0000981 or one of its children to appropriate DbTFs (Figure 1A, terms shaded green). This requires that the composite functional aspects of DbTF proteins—specific DNA binding and transcription regulation— must each be represented by their proper Molecular Function (MF) and Biological Process (BP) GO terms

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Summary

Original article

Gene Ontology annotation of sequence-specific DNA binding transcription factors: setting the stage for a large-scale curation effort. Citation details: Tripathi,S., Christie,K.R., Balakrishnana,R., et al Gene ontology annotation of sequence-specific DNA binding transcription factors: setting the stage for a large scale curation effort. Within a collaborative biocuration effort involving the user community, we are in the process of exhaustively annotating the full repertoire of human, mouse and rat proteins that qualify as DbTFs in as much as they are experimentally documented in the biomedical literature today. The completion of this task will significantly enrich Gene Ontology-based information resources for the research community

Introduction
Criteria that qualify a DbTF
When the functional unit of a TF is a complex
RNA polymerase II transcripƟon factor acƟvity
Evidence codes and experimental assays
TF activity
Evidence code
IDA IDA
Ribonuclease protecƟon assay
Work flow of annotation
YES Gene Ontology
Findings
Concluding remarks
Full Text
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