Evidence map›Paper›PMID 21724831›Full record

ArticleGenes & development2011

Integrative analysis of gene amplification in Drosophila follicle cells: parameters of origin activation and repression.

Jane C Kim, Jared Nordman, Fang Xie, Helena Kashevsky, Thomas Eng, Sharon Li, David M MacAlpine, Terry L Orr-Weaver

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing 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

42 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Finishing the egg.Genetics · 2024
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  14. Polyteny: still a giant player in chromosome research.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2017
    Review
  15. Review
  16. Article
  17. Multiple mechanisms contribute to double-strand break repair at rereplication forks in Drosophila follicle cells.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  18. 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

8 authors at 3 institutions in 1 country.

Jane C KimWhitehead Institute, Cambridge, Massachusetts 02142, USA.
Jared Nordman
Fang Xie
Helena Kashevsky
Thomas Eng
Sharon Li
David M MacAlpine
Terry L Orr-Weaver
Whitehead Institute for Biomedical Research · USMassachusetts Institute of Technology · USDuke University Hospital · US

Funding

REGULATION OF THE ENDO CELL CYCLE IN DROSOPHILAR01GM057960 · NIGMS · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI ORR-WEAVER, TERRY L. · 1999 to 2015
$5.3M
The Systematic Identification and Analysis of Replication Origins in DrosophilaU01HG004279 · NHGRI · DUKE UNIVERSITY · PI MACALPINE, DAVID M · 2007 to 2011
$2.6M
NHGRI NIH HHS 1U01HG004279NHGRI NIH HHS U01 HG004279NIGMS NIH HHS GM57960NIGMS NIH HHS R01 GM057960
6 · The paper itself

Abstract

In metazoans, how replication origins are specified and subsequently activated is not well understood. Drosophila amplicons in follicle cells (DAFCs) are genomic regions that undergo rereplication to increase DNA copy number. We identified all DAFCs by comparative genomic hybridization, uncovering two new amplicons in addition to four known previously. The complete identification of all DAFCs enabled us to investigate these in vivo replicons with respect to parameters of transcription, localization of the origin recognition complex (ORC), and histone acetylation, yielding important insights into gene amplification as a metazoan replication model. Significantly, ORC is bound across domains spanning 10 or more kilobases at the DAFC rather than at a specific site. Additionally, ORC is bound at many regions that do not undergo amplification, and, in contrast to cell culture, these regions do not correlate with high gene expression. As a developmental strategy, gene amplification is not the predominant means of achieving high expression levels, even in cells capable of amplification. Intriguingly, we found that, in some strains, a new amplicon, DAFC-22B, does not amplify, a consequence of distant repression of ORC binding and origin activation. This repression is alleviated when a fragment containing the origin is placed in different genomic contexts.

Indexed as

Gene AmplificationGene Expression RegulationAcetylationAnimalsDrosophila melanogasterHistonesOrigin Recognition ComplexProtein BindingProtein Structure, TertiaryHistonesOrigin Recognition Complex

Identifiers

PMID21724831
PMCPMC3134082
OpenAlexW2118567928

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.