Evidence map›Paper›PMID 16506100›Full record

ReviewChromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology2006

Chromatin dynamics and the evolution of alternate promoter states.

Gordon L Hager, Cem Elbi, Thomas A Johnson, Ty Voss, Akhilesh K Nagaich, R Louis Schiltz, Yi Qiu, Sam John

Abstract readReview
PubMed Publisher
In one paragraph

Review in Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Review
  2. Article
  3. Discontinuous transcription.Nucleus (Austin, Tex.) · 2018
    Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Quantitative analysis of genome-wide chromatin remodeling.Methods in molecular biology (Clifton, N.J.) · 2012
    Article
  12. Review
  13. What do expression dynamics tell us about the mechanism of transcription?Current opinion in genetics & development · 2011
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Genome-wide mechanisms of nuclear receptor action.Trends in endocrinology and metabolism: TEM · 2010
    Review
  20. Article
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

8 authors.

Gordon L HagerLaboratory of Receptor Biology and Gene Expression, Center for Cancer Research, National Cancer Institute, NIH, Building 41, Room B602, Bethesda, MD 20892-5055, USA. hagerg@exchange.nih.gov
Cem Elbi
Thomas A Johnson
Ty Voss
Akhilesh K Nagaich
R Louis Schiltz
Yi Qiu
Sam John

Funding

Chromatin Structure and Gene ExpressionZIABC005450 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HAGER, GORDON L · 2009 to 2025
$35.2M
CHROMATIN STRUCTURE AND GENE EXPRESSIONZ01BC005450 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HAGER, GORDON · 1996 to 2008
$1.7M
Intramural NIH HHS
6 · The paper itself

Abstract

Eucaryotic gene transcriptional switches utilize changes both in the activity and composition of soluble transcription factor complexes, and epigenetic modifications to the chromatin template. Until recently, alternate states of promoter activity have been associated with the assembly of relatively stable multiprotein complexes on target genes, with transitions in the composition of these complexes occurring on the time scale of minutes or hours. The development of living cell techniques to characterize transcription factor function in real time has led to an alternate view of highly dynamic protein/template interactions. In addition, emerging evidence suggests that energy-dependent processes contribute significantly to the rapid movement of proteins in living cells, and to the exchange of sequence-specific DNA-binding proteins with regulatory elements. Potential mechanisms involved in the unexpectedly rapid flux of factor/template interactions are discussed in the context of a "return-to-template" model for transcription factor function.

Indexed as

Promoter Regions, GeneticTranscription, GeneticAnimalsChromatinChromatin Assembly and DisassemblyEvolution, MolecularGene Expression RegulationHumansMolecular ChaperonesNuclear ProteinsReceptors, Cytoplasmic and NuclearChromatinMolecular ChaperonesNuclear ProteinsReceptors, Cytoplasmic and Nuclear

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.