Mapping Regulatory Elements by DNaseI Hypersensitivity Chip (DNase-Chip)
- 29 May 2009
- book chapter
- Published by Springer Nature
- Vol. 556, 177-190
- https://doi.org/10.1007/978-1-60327-192-9_13
Abstract
Historically, the simplest method to robustly identify active gene regulatory elements has been enzymatic digestion of nuclear DNA by nucleases such as DNaseI. Regions of extreme chromatin accessibility to DNaseI, commonly known as DNaseI hypersensitive sites, have been repeatedly shown to be markers for all types of active cis-acting regulatory elements, including promoters, enhancers, silencers, insulators, and locus control regions. However, the original classical method, which for over 25 years relied on Southern blot, was limited to studying only small regions of the genome. Here we describe the detailed protocol for DNase-chip, a high-throughput method that allows for a targeted or genome-wide identification of cis-acting gene regulatory elements.Keywords
This publication has 11 references indexed in Scilit:
- High-Resolution Mapping and Characterization of Open Chromatin across the GenomeCell, 2008
- Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot projectNature, 2007
- DNase-chip: a high-resolution method to identify DNase I hypersensitive sites using tiled microarraysNature Methods, 2006
- Identifying gene regulatory elements by genome-wide recovery of DNase hypersensitive sitesProceedings of the National Academy of Sciences, 2004
- Controlling the double helixNature, 2003
- NUCLEASE HYPERSENSITIVE SITES IN CHROMATINAnnual Review of Biochemistry, 1988
- A 200 base pair region at the 5$prime; end of the chicken adult $beta;-globin gene is accessible to nuclease digestionCell, 1981
- DNase I hypersensitive sites in Drosophila chromatin occur at the 5' ends of regions of transcription.Proceedings of the National Academy of Sciences, 1981
- The 5′ ends of Drosophila heat shock genes in chromatin are hypersensitive to DNase INature, 1980
- Tissue-specific DNA cleavages in the globin chromatin domain introduced by DNAase ICell, 1980