Evidence map›Paper›PMID 1849273›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1991

Intracellular distribution of microinjected antisense oligonucleotides.

J P Leonetti, N Mechti, G Degols, C Gagnor, B Lebleu

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1991. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed
15.3field-weighted citation impact, top 1% 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

89 citing papers in PubMed, 367 citations in OpenAlex.

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  10. Quantification and real-time tracking of RNA in live cells using Sticky-flares.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  11. Article
  12. Review
  13. Article
  14. LNA-based oligonucleotide electrotransfer for miRNA inhibition.Molecular therapy : the journal of the American Society of Gene Therapy · 2012
    Article
  15. Review
  16. RNase H-mediated degradation of toxic RNA in myotonic dystrophy type 1.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  17. Review
  18. Article
  19. Article
  20. Article

29 more citing papers are in PubMed but not listed here.

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.

J P LeonettiLaboratoire de Biochimie des Protéines, URA 1191 Centre National de la Recherche Scientifique, Université Montpellier II Sciences et Techniques du Languedoc, Montpellier, France.
N Mechti
G Degols
C Gagnor
B Lebleu
Université de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antisense oligomers constitute an attractive class of specific tools for genetic analysis and for potential therapeutic applications. Targets with different cellular locations have been described, such as mRNA translation initiation sites, pre-mRNA splicing sites, or the genes themselves. However the mechanism(s) of action and the intracellular distribution of antisense oligomers remain poorly understood. Antisense oligomers conjugated with various fluorochromes or with BrdUrd were microinjected into the cytoplasm of somatic cells, and their cellular distribution was monitored by fluorescence microscopy in fixed and nonfixed cells. A fast translocation in the nuclei and a concentration on nuclear structures were observed whatever probe was used. Nuclear transport occurs by diffusion since it is not affected by depletion of the intracellular ATP pool, temperature, or excess unlabeled oligomer. Accumulation of the oligomers in the nuclei essentially takes place on a set of proteins preferentially extracted between 0.2 M and 0.4 M NaCl as revealed by crosslinking of photosensitive oligomers. The relationship between nuclear location of antisense oligomers and their mechanism of action remains to be ascertained and could be of major interest in the design of more efficient antisense molecules.

Indexed as

AnimalsBase SequenceBiological TransportCapsidCell LineCell NucleusKineticsMicroinjectionsMolecular Sequence DataOligonucleotides, AntisenseRNA, MessengerVesicular stomatitis Indiana virusViral Core ProteinsOligonucleotides, AntisenseRNA, MessengerViral Core Proteins

Identifiers

PMID1849273
PMCPMC51306
OpenAlexW2082965230

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.