Evidence map›Paper›PMID 11121052›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2000

Developmentally dynamic histone acetylation pattern of a tissue-specific chromatin domain.

E C Forsberg, K M Downs, H M Christensen, H Im, P A Nuzzi, E H Bresnick

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 107 papers.

0numbers the graph read from it
0cells of the map it votes in
107citing papers in PubMed
6.6field-weighted citation impact, top 3% of its field
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

107 citing papers in PubMed, 226 citations in OpenAlex.

  1. Review
  2. Exploring epigenetic and microRNA approaches for γ-globin gene regulation.Experimental biology and medicine (Maywood, N.J.) · 2021
    Review
  3. Review
  4. Article
  5. Oncotarget · 2018
    Article
  6. Article
  7. Fetal haemoglobin induction in sickle cell disease.British journal of haematology · 2018
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

47 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

6 authors at 1 institution in 1 country.

E C ForsbergDepartment of Pharmacology, Molecular and Cellular Pharmacology Program, and Department of Anatomy, University of Wisconsin Medical School, 387 Medical Sciences Center, 1300 University Avenue, Madison, WI 53706, USA.
K M Downs
H M Christensen
H Im
P A Nuzzi
E H Bresnick
University of Wisconsin–Madison · US

Funding

Transcriptional Control of Hemoglobin Synthesis and Erythrocyte DevelopmentR01DK050107 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI Emery H. Bresnick · 1996 to 2026
$6.1M
Transcriptional Control of Hemoglobin SynthesisR37DK050107 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI BRESNICK, EMERY H · 2011 to 2020
$3.5M
COACTIVATORS THAT MEDIATE BETA GLOBIN LCR FUNCTIONR01DK055700 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI BRESNICK, EMERY H. · 1999 to 2006
$1.8M
VASCULOGENESIS IN THE MURINE ALLANTOISR29HD036847 · NICHD · UNIVERSITY OF WISCONSIN MADISON · PI DOWNS, KAREN M · 1998 to 2002
$307k
NICHD NIH HHS HD36847NICHD NIH HHS R29 HD036847NIDDK NIH HHS DK50107NIDDK NIH HHS DK55700NIDDK NIH HHS R01 DK050107NIDDK NIH HHS R01 DK055700NIDDK NIH HHS R37 DK050107
6 · The paper itself

Abstract

We have defined the histone acetylation pattern of the endogenous murine beta-globin domain, which contains the erythroidspecific beta-globin genes. The beta-globin locus control region (LCR) and transcriptionally active promoters were enriched in acetylated histones in fetal liver relative to fetal brain, whereas the inactive promoters were hypoacetylated. In contrast, the LCR and both active and inactive promoters were hyperacetylated in yolk sac. Hypersensitive site two of the LCR was also hyperacetylated in murine embryonic stem cells, whereas beta-globin promoters were hypoacetylated. Thus, the acetylation pattern varied at different developmental stages. Histone deacetylase inhibition selectively increased acetylation at a hypoacetylated promoter in fetal liver, suggesting that active deacetylation contributes to silencing of promoters. We propose that dynamic histone acetylation and deacetylation play an important role in the developmental control of beta-globin gene expression.

Indexed as

ChromatinLocus Control RegionSaccharomyces cerevisiae ProteinsAcetylationAcetyltransferasesAnimalsBinding SitesGlobinsHistone AcetyltransferasesHistonesLeukemia, Erythroblastic, AcuteLiverMicePromoter Regions, GeneticTumor Cells, CulturedAcetyltransferasesChromatinGlobinsHistone AcetyltransferasesHistonesSaccharomyces cerevisiae Proteins

Identifiers

PMID11121052
PMCPMC18947
OpenAlexW2044254819

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.