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Related Concept Videos

DNA Microarrays02:34

DNA Microarrays

Microarrays are high-throughput and relatively inexpensive assays that can be automated to analyze large quantities of data at a time. They are used in genome-wide studies to compare gene or protein expression under two varied conditions, such as healthy and diseased states. Microarrays consist of glass or silica slides on which probe molecules are covalently attached through surface functionalization. Most commonly, the slides are prepared through the chemisorption of silanes to silica...
Chromatin Immunoprecipitation- ChIP02:36

Chromatin Immunoprecipitation- ChIP

Chromatin immunoprecipitation, or ChIP, is an antibody-based technique used to identify sites on DNA that bind to transcription factors of interest or histone proteins. It also helps determine the type of histone modifications such as acetylation, phosphorylation, or methylation.
Types of ChIP
ChIP can be divided into two types - X-ChIP and N-ChIP. X-ChIP involves in vivo cross-linking of histones and regulatory proteins to DNA, fragmenting the DNA by sonication, and isolating the protein-DNA...

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DNA-affinity-purified Chip (DAP-chip) Method to Determine Gene Targets for Bacterial Two component Regulatory Systems
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Mapping regulatory elements by DNaseI hypersensitivity chip (DNase-Chip).

Yoichiro Shibata1, Gregory E Crawford

  • 1Institute for Genome Sciences & Policy, Duke University, Durham, NC, USA.

Methods in Molecular Biology (Clifton, N.J.)
|June 3, 2009
PubMed
Summary
This summary is machine-generated.

DNaseI hypersensitive sites mark active gene regulatory elements. A new high-throughput DNase-chip method enables targeted or genome-wide identification of these crucial cis-acting elements.

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Last Updated: Jun 22, 2026

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Area of Science:

  • Genomics
  • Molecular Biology
  • Epigenetics

Background:

  • DNaseI hypersensitive sites are reliable markers for active gene regulatory elements like promoters and enhancers.
  • Traditional methods using Southern blots were limited to analyzing small genomic regions.

Purpose of the Study:

  • To introduce DNase-chip, a high-throughput method for identifying cis-acting gene regulatory elements.
  • To enable both targeted and genome-wide analysis of regulatory elements.

Main Methods:

  • Enzymatic digestion of nuclear DNA using DNaseI to identify accessible chromatin regions.
  • Adaptation of DNase-chip protocol for high-throughput analysis.

Main Results:

  • DNase-chip allows for the identification of cis-acting regulatory elements.
  • The method supports both targeted and genome-wide analyses.

Conclusions:

  • DNase-chip offers a scalable and efficient approach to map gene regulatory elements.
  • This method advances the study of gene regulation at a genomic scale.