Evidence map›Paper›PMID 20212109›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2010

Non-Ca2+-conducting Ca2+ channels in fish skeletal muscle excitation-contraction coupling.

Johann Schredelseker, Manisha Shrivastav, Anamika Dayal, Manfred Grabner

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

45 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. Pathogenic CaCommunications biology · 2026
    Article
  3. CaOpen biology · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Advances in CaChannels (Austin, Tex.) · 2023
    Review
  10. Article
  11. Review
  12. CaHandbook of experimental pharmacology · 2023
    Article
  13. Article
  14. Article
  15. CaThe FEBS journal · 2022
    Article
  16. Article
  17. Article
  18. Article
  19. Physiological and Pathological Relevance of Selective and Nonselective CaAdvances in experimental medicine and biology · 2021
    Article
  20. Skeletal muscle CaPflugers Archiv : European journal of physiology · 2020
    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

4 authors at 1 institution in 1 country.

Johann SchredelsekerDepartment of Medical Genetics, Molecular and Clinical Pharmacology, Division of Biochemical Pharmacology, Innsbruck Medical University, A-6020 Innsbruck, Austria.
Manisha Shrivastav
Anamika Dayal
Manfred Grabner
Innsbruck Medical University · AT

Funding

Austrian Science Fund FWF W 1101
6 · The paper itself

Abstract

During skeletal muscle excitation-contraction (EC) coupling, membrane depolarizations activate the sarcolemmal voltage-gated L-type Ca(2+) channel (Ca(V)1.1). Ca(V)1.1 in turn triggers opening of the sarcoplasmic Ca(2+) release channel (RyR1) via interchannel protein-protein interaction to release Ca(2+) for myofibril contraction. Simultaneously to this EC coupling process, a small and slowly activating Ca(2+) inward current through Ca(V)1.1 is found in mammalian skeletal myotubes. The role of this Ca(2+) influx, which is not immediately required for EC coupling, is still enigmatic. Interestingly, whole-cell patch clamp experiments on freshly dissociated skeletal muscle myotubes from zebrafish larvae revealed the lack of such Ca(2+) currents. We identified two distinct isoforms of the pore-forming Ca(V)1.1alpha(1S) subunit in zebrafish that are differentially expressed in superficial slow and deep fast musculature. Both do not conduct Ca(2+) but merely act as voltage sensors to trigger opening of two likewise tissue-specific isoforms of RyR1. We further show that non-Ca(2+) conductivity of both Ca(V)1.1alpha(1S) isoforms is a common trait of all higher teleosts. This non-Ca(2+) conductivity of Ca(V)1.1 positions teleosts at the most-derived position of an evolutionary trajectory. Though EC coupling in early chordate muscles is activated by the influx of extracellular Ca(2+), it evolved toward Ca(V)1.1-RyR1 protein-protein interaction with a relatively small and slow influx of external Ca(2+) in tetrapods. Finally, the Ca(V)1.1 Ca(2+) influx was completely eliminated in higher teleost fishes.

Indexed as

Amino Acid SequenceAnimalsCalcium Channels, L-TypeEvolution, MolecularExcitation Contraction CouplingFishesIn Vitro TechniquesMolecular Sequence DataMuscle ContractionMuscle, SkeletalPatch-Clamp TechniquesPhylogenyProtein IsoformsProtein SubunitsRyanodine Receptor Calcium Release ChannelSequence Homology, Amino AcidCalcium Channels, L-TypeProtein IsoformsProtein SubunitsRyanodine Receptor Calcium Release ChannelZebrafish Proteins

Identifiers

PMID20212109
PMCPMC2851825
OpenAlexW2096994442

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.