PUBLICATION
Genome wide screens in yeast to identify potential binding sites and target genes of DNA-binding proteins
- Authors
- Zeng, J., Yan, J., Wang, T., Mosbrook-Davis, D., Dolan, K.T., Christensen, R., Stormo, G.D., Haussler, D., Lathrop, R.H., Brachmann, R.K., and Burgess, S.M.
- ID
- ZDB-PUB-071227-1
- Date
- 2008
- Source
- Nucleic acids research 36(1): e8 (Journal)
- Registered Authors
- Burgess, Shawn, Yan, Jizhou
- Keywords
- none
- MeSH Terms
-
- Animals
- Base Sequence
- Binding Sites
- Computational Biology
- Consensus Sequence
- DNA/chemistry
- DNA-Binding Proteins/metabolism*
- Forkhead Transcription Factors/metabolism
- Genomic Library
- Genomics/methods*
- Mice
- Plasmids/genetics
- Regulatory Elements, Transcriptional*
- Saccharomyces cerevisiae/genetics*
- Transcription Factors/metabolism*
- Tumor Suppressor Protein p53/metabolism
- Zebrafish/genetics
- Zebrafish Proteins/metabolism
- PubMed
- 18086703 Full text @ Nucleic Acids Res.
Citation
Zeng, J., Yan, J., Wang, T., Mosbrook-Davis, D., Dolan, K.T., Christensen, R., Stormo, G.D., Haussler, D., Lathrop, R.H., Brachmann, R.K., and Burgess, S.M. (2008) Genome wide screens in yeast to identify potential binding sites and target genes of DNA-binding proteins. Nucleic acids research. 36(1):e8.
Abstract
Knowledge of all binding sites for transcriptional activators and repressors is essential for computationally aided identification of transcriptional networks. The techniques developed for defining the binding sites of transcription factors tend to be cumbersome and not adaptable to high throughput. We refined a versatile yeast strategy to rapidly and efficiently identify genomic targets of DNA-binding proteins. Yeast expressing a transcription factor is mated to yeast containing a library of genomic fragments cloned upstream of the reporter gene URA3. DNA fragments with target-binding sites are identified by growth of yeast clones in media lacking uracil. The experimental approach was validated with the tumor suppressor protein p53 and the forkhead protein FoxI1 using genomic libraries for zebrafish and mouse generated by shotgun cloning of short genomic fragments. Computational analysis of the genomic fragments recapitulated the published consensus-binding site for each protein. Identified fragments were mapped to identify the genomic context of each binding site. Our yeast screening strategy, combined with bioinformatics approaches, will allow both detailed and high-throughput characterization of transcription factors, scalable to the analysis of all putative DNA-binding proteins.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping