Evidence map›Paper›PMID 10846109›Full record

ArticleJournal of virology2000

DNA sequence motifs which direct adeno-associated virus site-specific integration in a model system.

P Meneses, K I Berns, E Winocour

Abstract read
In one paragraph

Article in Journal of virology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

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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.

P MenesesDepartment of Pathology, Harvard Medical School, Boston, MA 02215, USA.
K I Berns
E Winocour

Funding

REGULATION OF AAV DNA REPLICATIONR01GM050032 · NIGMS · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI BERNS, KENNETH IRA · 1993 to 2000
$232k
NIAID NIH HHS AI 122251NIGMS NIH HHS GM50032
6 · The paper itself

Abstract

The DNA sequence motifs which direct adeno-associated virus type 2 site-specific integration are being investigated using a shuttle vector, propagated as a stable episome in cultured cell lines, as the target for integration. Previously, we reported that the minimum episomal targeting elements comprise a 16-bp binding motif (Rep binding site [RBS]) for a viral regulatory protein (Rep) separated by a short DNA spacer from a sequence (terminal resolution site [TRS]) that can serve as a substrate for Rep-mediated nicking activity (R. M. Linden, P. Ward, C. Giraud, E. Winocour, and K. I. Berns, Proc. Natl. Acad. Sci. USA 93:11288-11294, 1996; R. M. Linden, E. Winocour, and K. I. Berns, Proc. Natl. Acad. Sci. USA 93:7966-7972, 1996). We now report that episomal integration depends upon both the sequence and the position of the spacer DNA separating the RBS and TRS motifs. The spacer thus constitutes a third element required for site-specific episomal integration.

Indexed as

DNA, ViralVirus IntegrationBinding SitesCell Line, TransformedDependovirusDNA-Binding ProteinsDNA HelicasesHumansModels, BiologicalMutagenesis, Site-DirectedViral ProteinsDNA-Binding ProteinsDNA HelicasesDNA, Viralrep proteins, Adeno-associated virus 2Viral Proteins

Identifiers

PMID10846109
PMCPMC112124

What OpenQuestion holds

Textmetadata
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Registered trials

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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.