Evidence map›Paper›PMID 27226626›Full record

ArticleThe Journal of biological chemistry2016

Characterization of C-terminal Splice Variants of Cav1.4 Ca2+ Channels in Human Retina.

Françoise Haeseleer, Brittany Williams, Amy Lee

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

27 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. L-Type Voltage-Gated CaBiochemistry · 2025
    Article
  6. Article
  7. Review
  8. Calcium Channels in Retinal Function and Disease.Annual review of vision science · 2022
    Review
  9. Article
  10. Cav1.4 dysfunction and congenital stationary night blindness type 2.Pflugers Archiv : European journal of physiology · 2021
    Review
  11. Transmission at rod and cone ribbon synapses in the retina.Pflugers Archiv : European journal of physiology · 2021
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Transgenic Expression ofTranslational vision science & technology · 2020
    Article
  17. Article
  18. Review
  19. Circadian regulation in the retina: From molecules to network.The European journal of neuroscience · 2020
    Review
  20. Review
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

3 authors at 2 institutions in 1 country.

Françoise HaeseleerFrom the Department of Physiology and Biophysics, University of Washington, Seattle, Washington 98195 and.
Brittany Williamsthe Departments of Molecular Physiology and Biophysics, Interdisciplinary Graduate Program in Neuroscience, University of Iowa, Iowa City, Iowa 52242.
Amy Leethe Departments of Molecular Physiology and Biophysics, Otolaryngology Head-Neck Surgery, Neurology, and amy-lee@uiowa.edu.
University of Iowa · USUniversity of Washington · US

Funding

Regulation of auditory calcium channelsR01DC009433 · NIDCD · UNIVERSITY OF IOWA · PI LEE, AMY · 2009 to 2018
$3.6M
Regulation of Neuronal Calcium ChannelsR01NS084190 · NINDS · UNIVERSITY OF IOWA · PI LEE, AMY · 2014 to 2018
$2.2M
Regulation of L-type calcium channels by CaBP4R01EY020850 · NEI · UNIVERSITY OF WASHINGTON · PI HAESELEER, FRANCOISE J · 2010 to 2014
$1.6M
Regulation of auditory calcium channelsR55DC009433 · NIDCD · EMORY UNIVERSITY · PI LEE, AMY · 2008 to 2008
$100k
NEI NIH HHS R01 EY020850NIDCD NIH HHS R01 DC009433NIDCD NIH HHS R55 DC009433NINDS NIH HHS R01 NS084190
6 · The paper itself

Abstract

Voltage-gated Ca(2+) channels (Cav) undergo extensive alternative splicing that greatly enhances their functional diversity in excitable cells. Here, we characterized novel splice variants of the cytoplasmic C-terminal domain of Cav1.4 Ca(2+) channels that regulate neurotransmitter release in photoreceptors in the retina. These variants lack a portion of exon 45 and/or the entire exon 47 (Cav1.4Δex p45, Cav1.4Δex 47, Cav1.4Δex p45,47) and are expressed in the retina of primates but not mice. Although the electrophysiological properties of Cav1.4Δex p45 are similar to those of full-length channels (Cav1.4FL), skipping of exon 47 dramatically alters Cav1.4 function. Deletion of exon 47 removes part of a C-terminal automodulatory domain (CTM) previously shown to suppress Ca(2+)-dependent inactivation (CDI) and to cause a positive shift in the voltage dependence of channel activation. Exon 47 is crucial for these effects of the CTM because variants lacking this exon show intense CDI and activate at more hyperpolarized voltages than Cav1.4FL The robust CDI of Cav1.4Δex 47 is suppressed by CaBP4, a regulator of Cav1.4 channels in photoreceptors. Although CaBP4 enhances activation of Cav1.4FL, Cav1.4Δex 47 shows similar voltage-dependent activation in the presence and absence of CaBP4. We conclude that exon 47 encodes structural determinants that regulate CDI and voltage-dependent activation of Cav1.4, and is necessary for modulation of channel activation by CaBP4.

Indexed as

ExonsAlternative SplicingAnimalsCalcium-Binding ProteinsCalcium Channels, L-TypeHumansIon Channel GatingMacaca nemestrinaMiceRetinaCABP4 protein, humanCACNA1F protein, humanCalcium-Binding ProteinsCalcium Channels, L-Typecalcium-binding proteincalcium channelelectrophysiologyphotoreceptorretina

Identifiers

PMID27226626
PMCPMC4957050
OpenAlexW2398048693

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.