Evidence map›Paper›PMID 17376526›Full record

ReviewCell calcium2007

Physiological roles of STIM1 and Orai1 homologs and CRAC channels in the genetic model organism Caenorhabditis elegans.

Kevin Strange, Xiaohui Yan, Catherine Lorin-Nebel, Juan Xing

Abstract readReview
In one paragraph

Review in Cell calcium, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Lighting Up CaCells · 2021
    Review
  3. Hydrogen sulfide, oxygen, and calcium regulation in developing human airway smooth muscle.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  4. Distinct gating mechanism of SOC channel involving STIM-Orai coupling and an intramolecular interaction of Orai inProceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  5. Defective Store-Operated Calcium Entry Causes Partial Nephrogenic Diabetes Insipidus.Journal of the American Society of Nephrology : JASN · 2016
    Article
  6. Review
  7. Article
  8. STIM proteins: dynamic calcium signal transducers.Nature reviews. Molecular cell biology · 2012
    Review
  9. Taurine reduces ER stress in C. elegans.Journal of biomedical science · 2010
    Article
  10. Review
  11. Ca2+-stores in sperm: their identities and functions.Reproduction (Cambridge, England) · 2009
    Review
  12. Review
  13. 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

4 authors at 1 institution in 1 country.

Kevin StrangeDepartment of Anesthesiology, Vanderbilt University Medical Center, Nashville, TN 37232-2520, United States. kevin.strange@vanderbilt.edu
Xiaohui Yan
Catherine Lorin-Nebel
Juan Xing
Vanderbilt University Medical Center · US

Funding

Structure-function analysis of the volume-regulated anion channel VRAC using novel LRRC8 chimerasR01DK051610 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DENTON, JEROD S. · 1996 to 2025
$8.9M
Oscillatory Ca2+ signaling in the C.elegans intestineR01GM074229 · NIGMS · VANDERBILT UNIVERSITY · PI STRANGE, KEVIN · 2006 to 2009
$1.1M
NIDDK NIH HHS DK51610NIDDK NIH HHS R01 DK051610NIGMS NIH HHS GM74229NIGMS NIH HHS R01 GM074229
6 · The paper itself

Abstract

The nematode Caenorhabditis elegans provides numerous experimental advantages for developing an integrative molecular understanding of physiological processes and has proven to be a valuable model for characterizing Ca(2+) signaling mechanisms. This review will focus on the role of Ca(2+) release activated Ca(2+) (CRAC) channel activity in function of the worm gonad and intestine. Inositol 1,4,5-trisphosphate (IP(3))-dependent oscillatory Ca(2+) signaling regulates contractile activity of the gonad and rhythmic posterior body wall muscle contraction (pBoc) required for ovulation and defecation, respectively. The C. elegans genome contains a single homolog of both STIM1 and Orai1, proteins required for CRAC channel function in mammalian and Drosophila cells. C. elegans STIM-1 and ORAI-1 are coexpressed in the worm gonad and intestine and give rise to robust CRAC channel activity when coexpressed in HEK293 cells. STIM-1 or ORAI-1 knockdown causes complete sterility demonstrating that the genes are essential components of gonad Ca(2+) signaling. Knockdown of either protein dramatically inhibits intestinal cell CRAC channel activity, but surprisingly has no effect on pBoc, intestinal Ca(2+) oscillations or intestinal ER Ca(2+) store homeostasis. CRAC channels thus do not play obligate roles in all IP(3)-dependent signaling processes in C. elegans. Instead, we suggest that CRAC channels carry out highly specialized and cell specific signaling roles and that they may function as a failsafe mechanism to prevent Ca(2+) store depletion under pathophysiological and stress conditions.

Indexed as

Amino Acid SequenceAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCalcium ChannelsCalcium SignalingGonadsIntestinesMembrane ProteinsModels, GeneticMolecular Sequence DataORAI1 ProteinStromal Interaction Molecule 1Caenorhabditis elegans ProteinsCalcium ChannelsMembrane ProteinsORAI1 ProteinORAI-1 protein, C elegansstim-1 protein, C elegansStromal Interaction Molecule 1

Identifiers

PMID17376526
PMCPMC2066184
OpenAlexW1975808149

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.