Evidence map›Paper›PMID 17043110›Full record

ArticleMolecular and cellular biology2007

Drosophila dCBP is involved in establishing the DNA replication checkpoint.

Sarah Smolik, Kristen Jones

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

13 citing papers in PubMed, 23 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

2 authors at 1 institution in 1 country.

Sarah SmolikOregon Health and Sciences University, NRC3, 3181 SW Sam Jackson Park Road, Portland, OR 97239, USA. smoliks@ohsu.edu
Kristen Jones
Oregon Health & Science University · US

Funding

Chromatin Modulation and Transcription in DevelopmentR01GM061837 · NIGMS · OREGON HEALTH AND SCIENCE UNIVERSITY · PI SMOLIK, SARAH M · 2001 to 2004
$948k
NIGMS NIH HHS GM 61837NIGMS NIH HHS R01 GM061837
6 · The paper itself

Abstract

The CBP/p300 family of proteins comprises related acetyltransferases that coactivate signal-responsive transcription. Recent evidence suggests that p300/CBP may also interact directly with complexes that mediate different aspects of DNA metabolism such as replication and repair. In this report, we show that loss of dCBP in Drosophila cells and eye discs results in a defect in the cell cycle arrest induced by stalled DNA replication. We show that dCBP and the checkpoint kinase Mei-41 can be found together in a complex and, furthermore, that dCBP has a genetic interaction with mei-41 in the response to stalled DNA replication. These observations suggest a broader role for the p300/CBP acetyltransferases in the modulation of chromatin structure and function during DNA metabolic events as well as for transcription.

Indexed as

DNA ReplicationAnimalsCell Cycle ProteinsChromatinDNA RepairDrosophila melanogasterDrosophila ProteinsGenomeHeterozygoteHomozygoteModels, Geneticp300-CBP Transcription FactorsProtein Serine-Threonine KinasesRNA, Small InterferingSignal TransductionS PhaseCell Cycle ProteinsChromatinDrosophila ProteinsMei-41 protein, Drosophilap300-CBP Transcription FactorsProtein Serine-Threonine KinasesRNA, Small Interfering

Identifiers

PMID17043110
PMCPMC1800657
OpenAlexW1985648073

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.