Evidence map›Paper›PMID 21081924›Full record

ArticleMolecular systems biology2010

Quantitative analysis of the transcription control mechanism.

Changhui Mao, Christopher R Brown, Elena Falkovskaia, Shawfeng Dong, Eva Hrabeta-Robinson, Lauren Wenger, Hinrich Boeger

Abstract read
In one paragraph

Article in Molecular systems biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Nucleosomal proofreading of activator-promoter interactions.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Nucleosomal promoter variation generates gene expression noise.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  14. Nucleosomes, transcription, and probability.Molecular biology of the cell · 2014
    Article
  15. Single-cell nucleosome mapping reveals the molecular basis of gene expression heterogeneity.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  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

7 authors.

Changhui MaoDepartment of Molecular, Cell, and Developmental Biology, University of California Santa Cruz, Santa Cruz, CA 95064, USA.
Christopher R Brown
Elena Falkovskaia
Shawfeng Dong
Eva Hrabeta-Robinson
Lauren Wenger
Hinrich Boeger

Funding

Dynamics and Function of Signal-Induced Nucleosome DisassemblyR01GM078111 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI BOEGER, HANNS HINRICH · 2006 to 2010
$1.4M
Investigation of the PHO5 promoter chromatic transitionF32GM087867 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI BROWN, CHRISTOPHER RICHARD · 2009 to 2011
$151k
NIGMS NIH HHS F32 GM087867NIGMS NIH HHS F32GM087867NIGMS NIH HHS GM078111-01NIGMS NIH HHS R01 GM078111
6 · The paper itself

Abstract

Gene transcription requires a sequence of promoter state transitions, including chromatin remodeling, assembly of the transcription machinery, and clearance of the promoter by RNA polymerase. The rate-limiting steps in this sequence are regulated by transcriptional activators that bind at specific promoter elements. As the transition kinetics of individual promoters cannot be observed, the identity of the activator-controlled steps has remained a matter of speculation. In this study, we investigated promoter chromatin structure, and the intrinsic noise of expression over a wide range of expression values for the PHO5 gene of yeast. Interpretation of our results with regard to a stochastic model of promoter chromatin remodeling and gene expression suggests that the regulatory architecture of the gene expression process is measurably reflected in its intrinsic noise profile. Our chromatin structure and noise analyses indicate that the activator of PHO5 transcription stimulates the rates of promoter nucleosome disassembly, and assembly of the transcription machinery after nucleosome removal, but no other rates of the expression process.

Indexed as

Gene Expression Regulation, FungalTranscription, GeneticAcid PhosphataseChromatin Assembly and DisassemblyDNA-Binding ProteinsIn Situ Hybridization, FluorescenceModels, GeneticMutationNucleosomesPromoter Regions, GeneticRNA, MessengerSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSystems BiologyAcid PhosphataseDNA-Binding ProteinsNucleosomesPHO4 protein, S cerevisiaePHO5 protein, S cerevisiaeRNA, MessengerSaccharomyces cerevisiae Proteins

Identifiers

PMID21081924
PMCPMC3010110

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.