Evidence map›Paper›PMID 12134052›Full record

ArticleJournal of virology2002

Inserting a nuclear targeting signal into a replication-competent Moloney murine leukemia virus affects viral export and is not sufficient for cell cycle-independent infection.

Jennifer A Seamon, Kathryn S Jones, Christina Miller, Monica J Roth

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Optimal delivery of RNA interference by viral vectors for cancer therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Review
  2. Article
  3. Article
  4. Retroviral replicating vectors in cancer.Methods in enzymology · 2012
    Article
  5. Article
  6. Article
  7. Article
  8. 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

4 authors at 1 institution in 1 country.

Jennifer A SeamonDepartment of Biochemistry, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, Piscataway 08854, USA.
Kathryn S Jones
Christina Miller
Monica J Roth
Science Applications International Corporation (United States) · US

Funding

VIRUS-HOST INTERACTIONS IN EUKARYOTIC CELLST32AI007403 · NIAID · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI BREWER, GARY A. · 1991 to 2014
$1.7M
GRADUATE TRAINING IN CELLULAR AND MOLECULAR BIOLOGYT32GM008360 · NIGMS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI MADURA, KIRAN · 1991 to 2011
$1.1M
MECHANISM OF RETROVIRAL INTEGRATIONR01CA076545 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI ROTH, MONICA J · 1998 to 2000
$242k
MURINE RETROVIRAL VECTORS TARGETING NONDIVIDING CELLSR21DK054374 · NIDDK · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI ROTH, MONICA J · 1998 to 1999
–
NCI NIH HHS R01CA76545NIAID NIH HHS T32 AI007403NIAID NIH HHS T32-AI7403NIDDK NIH HHS R21-DK54374NIGMS NIH HHS T32 GM008360NIGMS NIH HHS T32-GM8360
6 · The paper itself

Abstract

The effects of inserting reported nuclear localization signals (NLSs) into the Moloney murine leukemia virus (Mo-MuLV) integrase (IN) protein, within a replication-competent viral construct, were studied. In contrast to the virus harboring IN fused to the simian virus 40 (SV40) large T antigen NLS (SV40 NLS) (J. A. Seamon, M. Adams, S. Sengupta, and M. J. Roth, Virology 274:412-419, 2000), a codon-modified SV40 NLS was stably expressed during viral propagation. Incorporation of the codon-modified SV40 NLS into IN, however, altered the packaging of the Gag-Pol precursor in the virus; viral particles contained decreased levels of reverse transcriptase (RT) and IN. In addition, the virus showed delayed kinetics of viral DNA synthesis upon infection. A panel of infectious MuLVs containing alternative IN-NLS fusions was generated and assayed for cell cycle-independent infection. Viral infection with the NLS-tagged proteins, however, remained dependent on passage of the cells through mitosis. This finding has direct implications for engineering murine-based retroviral vectors for gene therapy.

Indexed as

Amino Acid SequenceAnimalsAntigens, Polyomavirus TransformingBase SequenceCell CycleCell LineDNA ReplicationDNA, ViralDogsGenetic TherapyGenetic VectorsIntegrasesMiceMolecular Sequence DataMoloney murine leukemia virusNuclear Localization SignalsAntigens, Polyomavirus TransformingDNA, ViralIntegrasesNuclear Localization Signals

Identifiers

PMID12134052
PMCPMC155121
OpenAlexW2115030557

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.