Evidence map›Paper›PMID 17786200›Full record

ArticlePloS one2007

Regulation of retention of FosB intron 4 by PTB.

Victor Marinescu, Patricia A Loomis, Svetlana Ehmann, Mitchell Beales, Judith A Potashkin

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

17 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. ΔCannabis and cannabinoid research · 2017
    Article
  8. Lessons from non-canonical splicing.Nature reviews. Genetics · 2016
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Intron Retention and TE Exonization Events in ZRANB2.Comparative and functional genomics · 2012
    Article
  15. Article
  16. DNA-based MRI probes for specific detection of chronic exposure to amphetamine in living brains.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2009
    Article
  17. eNeuro
    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

5 authors at 1 institution in 1 country.

Victor MarinescuDepartment of Cellular and Molecular Pharmacology, The Chicago Medical School, Rosalind Franklin University of Medicine and Science, North Chicago, Illinois, United States of America.
Patricia A Loomis
Svetlana Ehmann
Mitchell Beales
Judith A Potashkin
Rosalind Franklin University of Medicine and Science · US

Funding

Cocaine Regulation of FosB SplicingR01DA015367 · NIDA · ROSALIND FRANKLIN UNIV OF MEDICINE &SCI · PI POTASHKIN, JUDITH · 2002 to 2004
$702k
COCAINE REGULATION OF FOSB SPLICINGR03DA013703 · NIDA · ROSALIND FRANKLIN UNIV OF MEDICINE &SCI · PI POTASHKIN, JUDITH · 2000 to 2001
$156k
NIDA NIH HHS DA-13703NIDA NIH HHS DA-15367NIDA NIH HHS R01 DA015367
6 · The paper itself

Abstract

One effect of stressors such as chronic drug administration is that sequence within the terminal exon of the transcription factor FosB is recognized as intronic and removed by alternative splicing. This results in an open-reading-frame shift that produces a translation stop codon and ultimately a truncated protein, termed DeltaFosB. In vitro splicing assays with control and mutated transcripts generated from a fosB mini-gene construct indicated a CU-rich sequence at the 3' end of intron 4 (I4) plays an important role in regulating fosB pre-mRNA splicing due to its binding of polypyrimidine tract binding protein (PTB). PTB binding to this sequence is dependent upon phosphorylation by protein kinase A and is blocked if the CU-rich sequence is mutated to a U-rich region. When this mutated fosB minigene is expressed in HeLa cells, the splicing efficiency of its product is increased compared to wild type. Moreover, transient transfection of PTB-1 in HeLa cells decreased the splicing efficiency of a wild type fosB minigene transcript. Depletion of PTB from nuclear extracts facilitated U2AF65 binding to wild type sequence in vitro, suggesting these proteins function in a dynamic equilibrium to modulate fosB pre-mRNA alternative splicing. These results demonstrate for the first time that phosphorylated PTB promotes intron retention and thereby silences the splicing of fosB I4.

Indexed as

IntronsAnimalsBase SequenceBinding SitesCyclic AMP-Dependent Protein KinasesGene Expression RegulationHeLa CellsHumansImmunoprecipitationPhosphorylationPolypyrimidine Tract-Binding ProteinProto-Oncogene Proteins c-fosRNA SplicingSequence Homology, Nucleic AcidCyclic AMP-Dependent Protein KinasesFOSB protein, humanPolypyrimidine Tract-Binding ProteinProto-Oncogene Proteins c-fos

Identifiers

PMID17786200
PMCPMC1952174
OpenAlexW1981836110

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.