Evidence map›Paper›PMID 15189860›Full record

ArticleBiophysical journal2004

Functional properties of the Drosophila melanogaster inositol 1,4,5-trisphosphate receptor mutants.

Sonal Srikanth, Zhengnan Wang, Huiping Tu, Shalima Nair, M K Mathew, Gaiti Hasan, Ilya Bezprozvanny

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

26 citing papers in PubMed, 46 citations in OpenAlex.

  1. Visual input drives diverse ER calcium signals in neuronsbioRxiv : the preprint server for biology · 2025
    Article
  2. Article
  3. Functional determination of calcium-binding sites required for the activation of inositol 1,4,5-trisphosphate receptors.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. IPDevelopment (Cambridge, England) · 2017
    Article
  9. Spontaneous CaFrontiers in molecular neuroscience · 2017
    Article
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  12. Article
  13. Article
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  15. Review
  16. Article
  17. Intracellular Ca2+ signaling and store-operated Ca2+ entry are required in Drosophila neurons for flight.Proceedings of the National Academy of Sciences of the United States of America · 2009
    Article
  18. Article
  19. 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

7 authors at 3 institutions in 2 countries.

Sonal SrikanthDepartment of Physiology, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas, USA.
Zhengnan Wang
Huiping Tu
Shalima Nair
M K Mathew
Gaiti Hasan
Ilya Bezprozvanny
The University of Texas Southwestern Medical Center · USNational Centre for Biological Sciences · INTata Institute of Fundamental Research · IN

Funding

STRUCTURE/FUNCTION OF INOSITOL TRISPHOSPHATE RECEPTORR01NS038082 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI BEZPROZVANNY, ILYA B · 1999 to 2009
$2.6M
NINDS NIH HHS R01 NS038082NINDS NIH HHS R01 NS38082
6 · The paper itself

Abstract

The inositol (1,4,5)-trisphosphate receptor (InsP(3)R) is an intracellular calcium (Ca(2+)) release channel that plays a crucial role in cell signaling. In Drosophila melanogaster a single InsP(3)R gene (itpr) encodes a protein (DmInsP(3)R) that is approximately 60% conserved with mammalian InsP(3)Rs. A number of itpr mutant alleles have been identified in genetic screens and studied for their effect on development and physiology. However, the functional properties of wild-type or mutant DmInsP(3)Rs have never been described. Here we use the planar lipid bilayer reconstitution technique to describe single-channel properties of embryonic and adult head DmInsP(3)R splice variants. The three mutants chosen in this study reside in each of the three structural domains of the DmInsP(3)R-the amino-terminal ligand binding domain (ug3), the middle-coupling domain (wc703), and the channel-forming region (ka901). We discovered that 1), the major functional properties of DmInsP(3)R (conductance, gating, and sensitivity to InsP(3) and Ca(2+)) are remarkably conserved with the mammalian InsP(3)R1; 2), single-channel conductance of the adult head DmInsP(3)R isoform is 89 pS and the embryonic DmInsP(3)R isoform is 70 pS; 3), ug3 mutation affects sensitivity of the DmInsP(3)Rs to activation by InsP(3), but not their InsP(3)-binding properties; 4), wc703 channels have increased sensitivity to modulation by Ca(2+); and 5), homomeric ka901 channels are not functional. We correlated the results obtained in planar lipid bilayer experiments with measurements of InsP(3)-induced Ca(2+) fluxes in microsomes isolated from wild-type and heterozygous itpr mutants. Our study validates the use of D. melanogaster as an appropriate model for InsP(3)R structure-function studies and provides novel insights into the fundamental mechanisms of the InsP(3)R function.

Indexed as

AnimalsCalciumCalcium ChannelsCells, CulturedDrosophila melanogasterInositolInositol 1,4,5-Trisphosphate ReceptorsIon Channel GatingLipid BilayersMutationReceptors, Cytoplasmic and NuclearCalciumCalcium ChannelsInositolInositol 1,4,5-Trisphosphate ReceptorsLipid BilayersReceptors, Cytoplasmic and Nuclear

Identifiers

PMID15189860
PMCPMC1304265
OpenAlexW2123849347

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.