Evidence map›Paper›PMID 14681192›Full record

ArticleDevelopment (Cambridge, England)2004

Both cyclin B levels and DNA-replication checkpoint control the early embryonic mitoses in Drosophila.

Jun-Yuan Ji, Jayne M Squirrell, Gerold Schubiger

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2004. 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
1.2field-weighted citation impact, top 23% 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, 46 citations in OpenAlex.

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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

3 authors at 2 institutions in 1 country.

Jun-Yuan JiDepartment of Biology, University of Washington, Seattle, WA 98195-1800, USA.
Jayne M Squirrell
Gerold Schubiger
University of Washington · USUniversity of Wisconsin–Madison · US

Funding

Regeneration of Imaginal Discs in DrosophilaR01GM058282 · NIGMS · UNIVERSITY OF WASHINGTON · PI BRADSHAW, H.D. TOBY · 1998 to 2010
$2.8M
NIGMS NIH HHS GM58282NIGMS NIH HHS R01 GM058282
6 · The paper itself

Abstract

The earliest embryonic mitoses in Drosophila, as in other animals except mammals, are viewed as synchronous and of equal duration. However, we observed that total cell-cycle length steadily increases after cycle 7, solely owing to the extension of interphase. Between cycle 7 and cycle 10, this extension is DNA-replication checkpoint independent, but correlates with the onset of Cyclin B oscillation. In addition, nuclei in the middle of embryos have longer metaphase and shorter anaphase than nuclei at the two polar regions. Interestingly, sister chromatids move faster in anaphase in the middle than the posterior region. These regional differences correlate with local differences in Cyclin B concentration. After cycle 10, interphase and total cycle duration of nuclei in the middle of the embryo are longer than at the poles. Because interphase also extends in checkpoint mutant (grapes) embryo after cycle 10, although less dramatic than wild-type embryos, interphase extension after cycle 10 is probably controlled by both Cyclin B limitation and the DNA-replication checkpoint.

Indexed as

DNA ReplicationAnimalsAnimals, Genetically ModifiedCDC2 Protein KinaseCell CycleChromatidsCyclin BDrosophila melanogasterDrosophila ProteinsGene DosageGenes, InsectGreen Fluorescent ProteinsHistonesLuminescent ProteinsMicroscopy, ConfocalMitosisCDC2 Protein KinaseCycB protein, DrosophilaCyclin BDrosophila ProteinsGreen Fluorescent ProteinsHistonesLuminescent ProteinsRecombinant Fusion Proteins

Identifiers

PMID14681192
PMCPMC3825093
OpenAlexW1992767260

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.