Evidence map›Paper›PMID 22049023›Full record

ArticleMolecular biology of the cell2012

Analysis of model replication origins in Drosophila reveals new aspects of the chromatin landscape and its relationship to origin activity and the prereplicative complex.

Jun Liu, Kristopher McConnell, Michael Dixon, Brian R Calvi

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

23 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. TheJournal of cell science · 2019
    Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Mechanisms and regulation of DNA replication initiation in eukaryotes.Critical reviews in biochemistry and molecular biology · 2017
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. DNA replication origin activation in space and time.Nature reviews. Molecular cell biology · 2015
    Review
  16. Review
  17. Review
  18. DNA replication origins.Cold Spring Harbor perspectives in biology · 2013
    Review
  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

4 authors at 1 institution in 1 country.

Jun LiuDepartment of Biology, Indiana University, Bloomington, IN 47405, USA.
Kristopher McConnell
Michael Dixon
Brian R Calvi
Carnegie Institution for Science · US

Funding

DISSECTION OF A METAZOAN PRE-REPLICATION COMPLEXR01GM061290 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI CALVI, BRIAN R · 2000 to 2009
$2.6M
Histone acetyltransferases in replication orgin activityF32GM080089 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI MCCONNELL, KRISTOPHER H · 2008 to 2010
$149k
NIGMS NIH HHS F32 GM080089NIGMS NIH HHS R01 GM061290NIGMS NIH HHS R01GM061290-10NIGMS NIH HHS R01GM061290-10S1
6 · The paper itself

Abstract

Epigenetic regulation exerts a major influence on origins of DNA replication during development. The mechanisms for this regulation, however, are poorly defined. We showed previously that acetylation of nucleosomes regulates the origins that mediate developmental gene amplification during Drosophila oogenesis. Here we show that developmental activation of these origins is associated with acetylation of multiple histone lysines. Although these modifications are not unique to origin loci, we find that the level of acetylation is higher at the active origins and quantitatively correlated with the number of times these origins initiate replication. All of these acetylation marks were developmentally dynamic, rapidly increasing with origin activation and rapidly declining when the origins shut off and neighboring promoters turn on. Fine-scale analysis of the origins revealed that both hyperacetylation of nucleosomes and binding of the origin recognition complex (ORC) occur in a broad domain and that acetylation is highest on nucleosomes adjacent to one side of the major site of replication initiation. It was surprising to find that acetylation of some lysines depends on binding of ORC to the origin, suggesting that multiple histone acetyltransferases may be recruited during origin licensing. Our results reveal new insights into the origin epigenetic landscape and lead us to propose a chromatin switch model to explain the coordination of origin and promoter activity during development.

Indexed as

DNA Replication TimingModels, GeneticAcetylationAnimalsChromatinDrosophilaDrosophila ProteinsEpigenesis, GeneticFemaleGene Expression Regulation, DevelopmentalHistone AcetyltransferasesHistonesMaleMultiprotein ComplexesNucleosomesOogenesisChromatinDrosophila ProteinsHistone AcetyltransferasesHistonesMultiprotein ComplexesNucleosomes

Identifiers

PMID22049023
PMCPMC3248898
OpenAlexW2166547494

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.