Evidence map›Paper›PMID 9482882›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1998

Presence and phosphorylation of transcription factors in developing dendrites.

P Crino, K Khodakhah, K Becker, S Ginsberg, S Hemby, J Eberwine

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

46 citing papers in PubMed, 150 citations in OpenAlex.

  1. Article
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  10. Bacterial expression and preliminary crystallographic studies of a 149-residue fragment of human Caprin-1.Acta crystallographica. Section F, Structural biology communications · 2015
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  12. The RNA-centred view of the synapse: non-coding RNAs and synaptic plasticity.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2014
    Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Quantitative biology of single neurons.Journal of the Royal Society, Interface · 2012
    Review
  18. Article
  19. 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

6 authors at 3 institutions in 1 country.

P CrinoDepartment of Pharmacology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.
K Khodakhah
K Becker
S Ginsberg
S Hemby
J Eberwine
University of Pennsylvania · USNational Human Genome Research Institute · USNational Institutes of Health · US

Funding

Gene expression in single aging neurons and gliaR37AG009900 · NIA · UNIVERSITY OF PENNSYLVANIA · PI EBERWINE, JAMES H · 2001 to 2010
$3.4M
GENE EXPRESSION IN SINGLE AGING NEURONS AND GLIAR01AG009900 · NIA · UNIVERSITY OF PENNSYLVANIA · PI EBERWINE, JAMES H · 1991 to 2000
$310k
NIA NIH HHS AG9900NIA NIH HHS R01 AG009900NIA NIH HHS R37 AG009900
6 · The paper itself

Abstract

In screening amplified poly(A) mRNA from hippocampal dendrites and growth cones in culture to determine candidates for local translation, we found that select transcription factor mRNAs were present. We hypothesized that synthesis of transcription factor proteins within dendrites would provide a direct signaling pathway between the distal dendrite and the nucleus resulting in modulation of gene expression important for neuronal differentiation. To evaluate this possibility, radiolabeled amplified antisense RNA was used to probe slot blots of transcription factor cDNAs as well as arrayed blots of zinc finger transcription factors. The mRNAs encoding the cAMP response element binding protein (CREB), zif 268, and one putative transcription factor were detected. We expanded upon these results showing that CREB protein is present in dendrites, that translation of CREB mRNA in isolated dendrites is feasible and that CREB protein found in dendrites can interact with the cis-acting cyclic AMP reponse element DNA sequence by using an in situ Southwestern assay. Further, CREB protein in dendrites is not transported to this site from the cell body because fluorescently tagged CREB microperfused into the soma did not diffuse into the dendrites. In addition, CREB protein microperfused into dendrites was rapidly transported to the nucleus, its likely site of bioactivity. Lastly, by using the isolated dendrite system we show that phosphorylation of Ser-133 on CREB protein can occur in isolated dendrites independent of the nucleus. These data provide a regulatory pathway in which transcription factors synthesized and posttranslationally modified in dendrites directly alter gene expression bypassing the integration of signal transduction pathways that converge on the nucleus.

Indexed as

Immediate-Early ProteinsAnimalsCells, CulturedCyclic AMP Response Element-Binding ProteinDendritesDNA-Binding ProteinsEarly Growth Response Protein 1Embryo, MammalianHippocampusNeuronsPhosphorylationRatsRecombinant ProteinsRNA, AntisenseRNA, MessengerRNA ProbesCyclic AMP Response Element-Binding ProteinDNA-Binding ProteinsEarly Growth Response Protein 1Egr1 protein, ratImmediate-Early ProteinsRecombinant ProteinsRNA, AntisenseRNA, MessengerRNA ProbesTranscription Factors

Identifiers

PMID9482882
PMCPMC19330
OpenAlexW2014378552

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.