Evidence map›Paper›PMID 8234283›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1993

Atrial G protein-activated K+ channel: expression cloning and molecular properties.

N Dascal, W Schreibmayer, N F Lim, W Wang, C Chavkin, L DiMagno, C Labarca, B L Kieffer, C Gaveriaux-Ruff, D Trollinger

Open access · greenAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed
15.5field-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

95 citing papers in PubMed, 359 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. G protein-gated inwardly rectifying KHistology and histopathology · 2025
    Review
  5. IiScience · 2022
    Article
  6. Neuronal G protein-gated KAmerican journal of physiology. Cell physiology · 2022
    Review
  7. A molecular switch controls the impact of cholesterol on a Kir channel.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. G Protein-Gated Potassium Channels: A Link to Drug Addiction.Trends in pharmacological sciences · 2017
    Review
  14. Review
  15. Review
  16. Article
  17. Firing modes of dopamine neurons drive bidirectional GIRK channel plasticity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  18. Article
  19. Article
  20. Article

35 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

10 authors at 1 institution in 1 country.

N DascalDivision of Biology, California Institute of Technology, Pasadena 91125.
W Schreibmayer
N F Lim
W Wang
C Chavkin
L DiMagno
C Labarca
B L Kieffer
C Gaveriaux-Ruff
D Trollinger
California Institute of Technology · US

Funding

SYNAPTIC TRANSMISSION AT A VERTEBRATE GIANT SYNAPSEP50MH049176 · NIMH · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI FRASER, SCOTT E · 1992 to 2001
$4.2M
INTRACELLULAR SECOND MESSENGERS, BIOPHYSICAL STUDIESR01GM029836 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI LESTER, HENRY A. · 1985 to 2002
$1.2M
NIGMS NIH HHS GM29836NIMH NIH HHS MH49176
6 · The paper itself

Abstract

Activity of several ion channels is controlled by heterotrimeric GTP-binding proteins (G proteins) via a membrane-delimited pathway that does not involve cytoplasmic intermediates. The best studied example is the K+ channel activated by muscarinic agonists in the atrium, which plays a crucial role in regulating the heartbeat. To enable studies of the molecular mechanisms of activation, this channel, denoted KGA, was cloned from a rat atrium cDNA library by functional coupling to coexpressed serotonin type 1A receptors in Xenopus oocytes. KGA displays regions of sequence homology to other inwardly rectifying channels as well as unique regions that may govern G-protein interaction. The expressed KGA channel is activated by serotonin 1A, muscarinic m2, and delta-opioid receptors via G proteins. KGA is activated by guanosine 5'-[gamma-thio]triphosphate in excised patches, confirming activation by a membrane-delimited pathway, and displays a conductance equal to that of the endogenous channel in atrial cells. The hypothesis that similar channels play a role in neuronal inhibition is supported by the cloning of a nearly identical channel (KGB1) from a rat brain cDNA library.

Indexed as

Amino Acid SequenceAnimalsBlotting, NorthernBrainCarbacholCloning, MolecularDNA, ComplementaryEvoked PotentialsGene ExpressionG Protein-Coupled Inwardly-Rectifying Potassium ChannelsGTP-Binding ProteinsGuanosine 5'-O-(3-Thiotriphosphate)Heart AtriaMembrane PotentialsMolecular Sequence DataMyocardiumCarbacholDNA, ComplementaryG Protein-Coupled Inwardly-Rectifying Potassium ChannelsGTP-Binding ProteinsGuanosine 5'-O-(3-Thiotriphosphate)Kcnj3 protein, ratPotassium ChannelsReceptors, MuscarinicReceptors, Opioid, deltaReceptors, SerotoninSerotonin

Identifiers

PMID8234283
PMCPMC47749
OpenAlexW2043327777

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.