Evidence map›Paper›PMID 11230508›Full record

ArticleThe Journal of physiology2001

Alternative splicing of KCNQ2 potassium channel transcripts contributes to the functional diversity of M-currents.

Z Pan, A A Selyanko, J K Hadley, D A Brown, J E Dixon, D McKinnon

Abstract readComparative Study
In one paragraph

Article in The Journal of physiology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
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

24 citing papers in PubMed.

  1. Trial
  2. Article
  3. Plural molecular and cellular mechanisms of pore domainbioRxiv : the preprint server for biology · 2024
    Article
  4. Heteromeric Kv7.2/7.3 channels differentially regulate action potential initiation and conduction in neocortical myelinated axons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. A common ankyrin-G-based mechanism retains KCNQ and NaV channels at electrically active domains of the axon.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2006
    Article
  14. Cholinergic suppression of KCNQ channel currents enhances excitability of striatal medium spiny neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2005
    Article
  15. Article
  16. Article
  17. KCNQ2 is a nodal K+ channel.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2004
    Article
  18. Article
  19. KCNQ/M currents in sensory neurons: significance for pain therapy.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2003
    Article
  20. 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

6 authors.

Z PanDepartment of Neurobiology and Behavior and Department of Physiology and Biophysics, State University of New York at Stony Brook, Stony Brook, NY 11794, USA.
A A Selyanko
J K Hadley
D A Brown
J E Dixon
D McKinnon

Funding

Support CoreP01HL028958 · NHLBI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI ROSEN, MICHAEL R. · 1985 to 2007
$17.6M
Molecular Physiology--Control of Firing PropertiesR01NS029755 · NINDS · STATE UNIVERSITY NEW YORK STONY BROOK · PI MCKINNON, DAVID · 1992 to 2004
$1.6M
CARDIOVASCULAR ROLE OF SYMPATHETIC K+ CHANNEL GENESR01HL061269 · NHLBI · STATE UNIVERSITY NEW YORK STONY BROOK · PI BRINK, PETER R · 2000 to 2003
$1.1M
NHLBI NIH HHS HL-2895816NHLBI NIH HHS HL-61269NINDS NIH HHS NS-29755NINDS NIH HHS R01 NS029755
6 · The paper itself

Abstract

The region of alternative splicing in the KCNQ2 potassium channel gene was determined by RNase protection analysis of KCNQ2 mRNA transcripts. Systematic analysis of KCNQ2 alternative splice variant expression in rat superior cervical ganglia revealed multiple variant isoforms. One class of KCNQ2 splice variants, those that contained exon 15a, was found to have significantly different kinetics to those of the other isoforms. These transcripts encoded channel subunits that, when co-expressed with the KCNQ3 subunit, activated and deactivated approximately 2.5 times more slowly than other isoforms. Deletion of exon 15a in these isoforms produced a reversion to the faster kinetics. Comparison of the kinetic properties of the cloned channel splice variants with those of the native M-current suggests that alternative splicing of the KCNQ2 gene may contribute to the variation in M-current kinetics seen in vivo.

Indexed as

Alternative SplicingTranscription, GeneticAmino Acid SequenceAnimalsBase SequenceCHO CellsCricetinaeDNA, ComplementaryExonsGene ExpressionKCNQ2 Potassium ChannelKineticsMolecular Sequence DataNeuronsPotassium Channel BlockersPotassium ChannelsDNA, ComplementaryKCNQ2 Potassium ChannelPotassium Channel BlockersPotassium ChannelsPotassium Channels, Voltage-GatedProtein IsoformsReceptors, Cholinergic

Identifiers

PMID11230508
PMCPMC2278468

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.