Evidence map›Paper›PMID 8016135›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1994

Efficient manipulation of the human adenovirus genome as an infectious yeast artificial chromosome clone.

G Ketner, F Spencer, S Tugendreich, C Connelly, P Hieter

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

52 citing papers in PubMed, 142 citations in OpenAlex.

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  9. SARS-CoV-2 variant spike and accessory gene mutations alter pathogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  10. SARS-CoV-2 Variant Spike and accessory gene mutations alter pathogenesis.bioRxiv : the preprint server for biology · 2022
    Article
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  13. Review
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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

5 authors at 1 institution in 1 country.

G KetnerDepartment of Immunology and Infectious Diseases, Johns Hopkins University School of Hygiene and Public Health, Baltimore, MD 21205.
F Spencer
S Tugendreich
C Connelly
P Hieter
Johns Hopkins University · US

Funding

TRANSPOSITION OF TN7P01CA016519 · NCI · JOHNS HOPKINS UNIVERSITY · PI BOEKE, JEF D · 1985 to 2010
$21.4M
UTILIZATION OF TRANSGENICS IN THE STUDY OF DOWN SYNDROMEP01HD024605 · NICHD · JOHNS HOPKINS UNIVERSITY · PI REEVES, ROGER H · 1989 to 2004
$8.2M
ADENOVIRUS GENE EXPRESSION: GENETICS OF EARLY REGION 4R01AI026239 · NIAID · JOHNS HOPKINS UNIVERSITY · PI KETNER, GARY W · 1991 to 1995
–
NCI NIH HHS CA16519NIAID NIH HHS AI26239NICHD NIH HHS HD24605
6 · The paper itself

Abstract

A yeast artificial chromosome (YAC) containing a complete human adenovirus type 2 genome was constructed, and viral DNA derived from the YAC was shown to be infectious upon introduction into mammalian cells. The adenovirus YAC could be manipulated efficiently using homologous recombination-based methods in the yeast host, and mutant viruses, including a variant that expresses the human analog of the Saccharomyces cerevisiae CDC27 gene, were readily recovered from modified derivatives of the YAC. The application of powerful yeast genetic techniques to an infectious adenovirus clone promises to significantly enhance the genetic analysis of adenovirus and to simplify the construction of adenovirus-based vectors for vaccines or for gene transfer to mammalian cells or whole animals. The adenovirus YAC was produced by homologous recombination in vivo between adenovirus 2 virion DNA and YAC vector plasmids carrying segments of the viral left and right genomic termini. This recombinational cloning strategy is generally applicable to the construction of YACs containing other DNA segments, such as the genomes of other viruses. Further, it is very efficient and may permit the targeted cloning of segments of the genomes of higher organisms directly from genomic DNA.

Indexed as

Cell Cycle ProteinsChromosomes, Artificial, YeastGenome, ViralAdenoviruses, HumanApc3 Subunit, Anaphase-Promoting Complex-CyclosomeBase SequenceCloning, MolecularDNA PrimersDNA, ViralFungal ProteinsGenes, FungalGenetic VectorsHumansMolecular Sequence DataPlasmidsPolymerase Chain ReactionApc3 Subunit, Anaphase-Promoting Complex-CyclosomeCDC27 protein, humanCDC27 protein, S cerevisiaeCell Cycle ProteinsDNA PrimersDNA, ViralFungal ProteinsSaccharomyces cerevisiae ProteinsUbiquitin-Protein Ligases

Identifiers

PMID8016135
PMCPMC44163
OpenAlexW2039040205

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.