Evidence map›Paper›PMID 2874558›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1986

In situ hybridization to localize mRNA encoding the neurotransmitter synthetic enzyme glutamate decarboxylase in mouse cerebellum.

C W Wuenschell, R S Fisher, D L Kaufman, A J Tobin

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1986. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
13.9field-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

15 citing papers in PubMed, 96 citations in OpenAlex.

  1. The Cerebellar Dopaminergic System.Frontiers in systems neuroscience · 2021
    Review
  2. Article
  3. Article
  4. Article
  5. GABAergic neurons in the central region of the spinal cord: a novel substrate for sympathetic inhibition.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2005
    Article
  6. Article
  7. Use-dependent modulation of inhibitory capacity in the feline lumbar spinal cord.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2002
    Article
  8. Presence of mRNA for glutamic acid decarboxylase in both excitatory and inhibitory neurons.Proceedings of the National Academy of Sciences of the United States of America · 1996
    Article
  9. Article
  10. Review
  11. Developmentally regulated expression of an exon containing a stop codon in the gene for glutamic acid decarboxylase.Proceedings of the National Academy of Sciences of the United States of America · 1990
    Article
  12. Pattern of expression of glutamic acid decarboxylase mRNA in the developing rat brain.Proceedings of the National Academy of Sciences of the United States of America · 1988
    Article
  13. Article
  14. Article
  15. 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.

C W Wuenschell
R S Fisher
D L Kaufman
A J Tobin
University of California, Los Angeles · US

Funding

GADS, GABA PRODUCTION, AND SEIZURE SUPPRESSIONR01NS022256 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TOBIN, ALLAN J · 1985 to 2002
$1.1M
GENE REGULATION IN CEREBELLUM DEVELOPMENTR01NS020356 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TOBIN, ALLAN J · 1985 to 1991
–
NIGMS NIH HHS GM 7104NINDS NIH HHS NS 20356NINDS NIH HHS NS 22256
6 · The paper itself

Abstract

Glutamate decarboxylase (GAD; EC 4.1.1.15) is responsible for the synthesis of the neurotransmitter gamma-aminobutyric acid (GABA). We have used a cDNA sequence encoding GAD to produce a single-stranded RNA hybridization probe for GAD mRNA. This probe detects GAD mRNA in individual cells in sections of mouse cerebellum. The specificity of in situ hybridization with this probe rests on four criteria: the distribution of labeled cells matched the results we and others obtain with GAD immunohistochemistry (Purkinje, Golgi II, stellate, and basket neurons were labeled, whereas granule cells and glia were not); a negative control probe having a sequence identical to GAD mRNA did not specifically label any cerebellar cells; prior treatment of the sections with RNase abolished specific labeling; the labeling showed the melting behavior typical of nucleic acid hybrids. Translation of GAD mRNA is apparently restricted to neuronal cell bodies since GAD mRNA was detectable in neuronal perikarya but not in terminals. Also, the choice of GABA as a neurotransmitter appears to be made at the level of transcription since granule neurons did not contain detectable GAD mRNA. The level of GAD mRNA varied among the classes of neurons as well as from cell to cell within each neuron type.

Indexed as

AnimalsAutoradiographyCerebellumCricetinaeGlutamate DecarboxylaseMiceMice, Inbred C57BLNeuronsNeurotransmitter AgentsNucleic Acid HybridizationRNA, MessengerSulfur RadioisotopesTranscription, GeneticUridine TriphosphateGlutamate DecarboxylaseNeurotransmitter AgentsRNA, MessengerSulfur RadioisotopesUridine Triphosphate

Identifiers

PMID2874558
PMCPMC386466
OpenAlexW2092792680

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.