Genome-Wide Mapping of in Vivo Protein-DNA Interactions
California Institute of Technology · Stanford University
Abstract
In vivo protein-DNA interactions connect each transcription factor with its direct targets to form a gene network scaffold. To map these protein-DNA interactions comprehensively across entire mammalian genomes, we developed a large-scale chromatin immunoprecipitation assay (ChIPSeq) based on direct ultrahigh-throughput DNA sequencing. This sequence census method was then used to map in vivo binding of the neuron-restrictive silencer factor (NRSF; also known as REST, for repressor element-1 silencing transcription factor) to 1946 locations in the human genome. The data display sharp resolution of binding position [+/-50 base pairs (bp)], which facilitated our finding motifs and allowed us to identify…
Citation impact
- FWCI
- 74.53
- Percentile
- 100%
- References
- 23
Authors
4Topics & keywords
- Biology
- Chromatin immunoprecipitation
- Transcription factor
- Genetics
- ChIP-sequencing
- Computational biology
- DNA binding site
- Repressor