Evidence map›Paper›PMID 19303047›Full record

ArticleMethods (San Diego, Calif.)2009

Isolation of active regulatory elements from eukaryotic chromatin using FAIRE (Formaldehyde Assisted Isolation of Regulatory Elements).

Paul G Giresi, Jason D Lieb

Abstract read
In one paragraph

Article in Methods (San Diego, Calif.), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 132 papers.

0numbers the graph read from it
0cells of the map it votes in
132citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

132 citing papers in PubMed.

  1. Trial
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  12. Exploitation of epigenetic variation of crop wild relatives for crop improvement and agrobiodiversity preservation.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2022
    Review
  13. Highly sensitive single-cell chromatin accessibility assay and transcriptome coassay with METATAC.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  14. Pioneer factors as master regulators of the epigenome and cell fate.Nature reviews. Molecular cell biology · 2022
    Review
  15. Article
  16. Article
  17. Review
  18. Mapping open chromatin by ATAC-seq in bread wheat.Frontiers in plant science · 2022
    Article
  19. Article
  20. Review

72 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Paul G GiresiDepartment of Biology and Carolina Center for the Genome Sciences, University of North Carolina at Chapel Hill, CB #3280, 408 Fordham Hall, Chapel Hill, NC 27599-3280, USA.
Jason D Lieb

Funding

Comprehensive Identification of Active Functional Elements in Human ChromatinU54HG004563 · NHGRI · DUKE UNIVERSITY · PI CRAWFORD, GREGORY E · 2007 to 2011
$9.7M
Uniting disparate fields to explore transcription factor binding dynamicsR01GM072518 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LIEB, JASON D · 2005 to 2014
$2.5M
NHGRI NIH HHS U54 HG004563NIGMS NIH HHS R01 GM072518
6 · The paper itself

Abstract

The binding of sequence-specific regulatory factors and the recruitment of chromatin remodeling activities cause nucleosomes to be evicted from chromatin in eukaryotic cells. Traditionally, these active sites have been identified experimentally through their sensitivity to nucleases. Here we describe the details of a simple procedure for the genome-wide isolation of nucleosome-depleted DNA from human chromatin, termed FAIRE (Formaldehyde Assisted Isolation of Regulatory Elements). We also provide protocols for different methods of detecting FAIRE-enriched DNA, including use of PCR, DNA microarrays, and next-generation sequencing. FAIRE works on all eukaryotic chromatin tested to date. To perform FAIRE, chromatin is crosslinked with formaldehyde, sheared by sonication, and phenol-chloroform extracted. Most genomic DNA is crosslinked to nucleosomes and is sequestered to the interphase, whereas DNA recovered in the aqueous phase corresponds to nucleosome-depleted regions of the genome. The isolated regions are largely coincident with the location of DNaseI hypersensitive sites, transcriptional start sites, enhancers, insulators, and active promoters. Given its speed and simplicity, FAIRE has utility in establishing chromatin profiles of diverse cell types in health and disease, isolating DNA regulatory elements en masse for further characterization, and as a screening assay for the effects of small molecules on chromatin organization.

Indexed as

Regulatory Sequences, Nucleic AcidChromatinChromosome MappingCross-Linking ReagentsDNAFormaldehydeGenomicsHumansOligonucleotide Array Sequence AnalysisChromatinCross-Linking ReagentsDNAFormaldehyde

Identifiers

PMID19303047
PMCPMC2710428

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.