Evidence map›Paper›PMID 19805124›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2009

Orai1 internalization and STIM1 clustering inhibition modulate SOCE inactivation during meiosis.

Fang Yu, Lu Sun, Khaled Machaca

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

59 citing papers in PubMed, 118 citations in OpenAlex.

  1. Article
  2. The signal that stimulates mammalian embryo development.Frontiers in cell and developmental biology · 2024
    Review
  3. Article
  4. Review
  5. Review
  6. CaJournal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  7. Review
  8. Article
  9. Review
  10. Soluble αKlotho downregulates Orai1-mediated store-operated CaPflugers Archiv : European journal of physiology · 2021
    Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Remodeling of ER-plasma membrane contact sites but not STIM1 phosphorylation inhibits CaProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  16. Constitutive IPJournal of cell science · 2019
    Article
  17. Article
  18. Article
  19. Ion Channel Function During Oocyte Maturation and Fertilization.Frontiers in cell and developmental biology · 2018
    Review
  20. Cholesterol modulates the cellular localization of Orai1 channels and its disposition among membrane domains.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2017
    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

3 authors at 1 institution in 1 country.

Fang YuDepartment of Physiology and Biophysics, Weill Cornell Medical College in Qatar (WCMC-Q), Education City-Qatar Foundation, Doha, Qatar.
Lu Sun
Khaled Machaca
Weill Cornell Medical College in Qatar · QA

Funding

REGULATION OF CA SIGNALING DURING OOGENESISR01GM061829 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI MACHACA, KHALED · 2000 to 2009
$1.8M
NIGMS NIH HHS GM061829NIGMS NIH HHS R01 GM061829
6 · The paper itself

Abstract

Store-operated Ca(2+) entry (SOCE) is a ubiquitous Ca(2+) influx pathway activated in response to depletion of intracellular Ca(2+) stores. SOCE is a primary modulator of intracellular Ca(2+) dynamics, which specify cellular responses. Interestingly, SOCE inactivates during M phase but the mechanisms involved remain unclear. SOCE is mediated by clustering of the ER Ca(2+) sensor STIM1 in response to Ca(2+) store depletion, leading to gating of the plasma membrane SOCE channel Orai1. Here we show that SOCE inactivation in meiosis is the result of internalization of Orai1 into an intracellular vesicular compartment and to the inability of STIM1 to cluster in response to store depletion. At rest, Orai1 continuously recycles between the cell membrane and an endosomal compartment. We further show that STIM1-STIM1 interactions are inhibited during meiosis, which appears to mediate the inability of STIM1 to form puncta following store depletion. In contrast, STIM1-Orai1 interactions remain functional during meiosis. Combined, the removal of Orai1 from the cell membrane and STIM1 clustering inhibition effectively uncouple store depletion from SOCE activation in meiosis. Although STIM1 is phosphorylated during meiosis, phosphomimetic and alanine substitution mutations do not modulate STIM1 clustering, arguing that phosphorylation does not mediate STIM1 clustering inhibition during meiosis.

Indexed as

AnimalsCalciumCell MembraneEndosomesFemaleKineticsMeiosisMembrane ProteinsMitosisOvumSynaptosomal-Associated Protein 25XenopusXenopus ProteinsCalciumMembrane ProteinsSynaptosomal-Associated Protein 25Xenopus Proteins

Identifiers

PMID19805124
PMCPMC2765092
OpenAlexW2118478876

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.