Evidence map›Paper›PMID 23148228›Full record

ArticleThe Journal of biological chemistry2013

Re-evaluation of the role of calcium homeostasis endoplasmic reticulum protein (CHERP) in cellular calcium signaling.

Yaping Lin-Moshier, Peter J Sebastian, Leeann Higgins, Natalie D Sampson, Jane E Hewitt, Jonathan S Marchant

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

58 citing papers in PubMed, 90 citations in OpenAlex.

  1. Review
  2. Article
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  9. Article
  10. CHERP Regulates the Alternative Splicing of pre-mRNAs in the Nucleus.International journal of molecular sciences · 2022
    Article
  11. Convergent evolution of a blood-red nectar pigment in vertebrate-pollinated flowers.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  12. Article
  13. Article
  14. Novel Insight into the Effects of CpxR onInternational journal of molecular sciences · 2021
    Article
  15. Formate-Dependent Heterodisulfide Reduction in aApplied and environmental microbiology · 2021
    Article
  16. Article
  17. Article
  18. Article
  19. Celiac Antigenicity of Ancient Wheat Species.Foods (Basel, Switzerland) · 2019
    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

6 authors at 2 institutions in 2 countries.

Yaping Lin-MoshierDepartment of Pharmacology, University of Minnesota Medical School, Minneapolis, Minnesota 55455, USA.
Peter J Sebastian
Leeann Higgins
Natalie D Sampson
Jane E Hewitt
Jonathan S Marchant
University of Minnesota Medical Center · USUniversity of Nottingham · GB

Funding

Functional architecture of IP3-evoked local Ca2+ signalsR01GM088790 · NIGMS · UNIVERSITY OF MINNESOTA · PI MARCHANT, JONATHAN S, SLAMA, JAMES T · 2009 to 2025
$4.7M
Biotechnology and Biological Sciences Research CouncilNIGMS NIH HHS GM088790NIGMS NIH HHS R01 GM088790
6 · The paper itself

Abstract

Changes in cytoplasmic Ca(2+) concentration, resulting from activation of intracellular Ca(2+) channels within the endoplasmic reticulum, regulate several aspects of cellular growth and differentiation. Ca(2+) homeostasis endoplasmic reticulum protein (CHERP) is a ubiquitously expressed protein that has been proposed as a regulator of both major families of endoplasmic reticulum Ca(2+) channels, inositol 1,4,5-trisphosphate receptors (IP(3)Rs) and ryanodine receptors (RyRs), with resulting effects on mitotic cycling. However, the manner by which CHERP regulates intracellular Ca(2+) channels to impact cellular growth is unknown. Here, we challenge previous findings that CHERP acts as a direct cytoplasmic regulator of IP(3)Rs and RyRs and propose that CHERP acts in the nucleus to impact cellular proliferation by regulating the function of the U2 snRNA spliceosomal complex. The previously reported effects of CHERP on cellular growth therefore are likely indirect effects of altered spliceosomal function, consistent with prior data showing that loss of function of U2 snRNP components can interfere with cell growth and induce cell cycle arrest.

Indexed as

Gene Expression RegulationAmino Acid SequenceCalciumCalcium SignalingCell CycleCell MembraneCytoplasmDNA-Binding ProteinsEndoplasmic ReticulumHEK293 CellsHomeostasisHumansInositol 1,4,5-Trisphosphate ReceptorsJurkat CellsMembrane ProteinsMolecular Sequence DataCalciumCHERP protein, humanDNA-Binding ProteinsInositol 1,4,5-Trisphosphate ReceptorsMembrane ProteinsNucleosomesRibonucleoproteinsRNA-Binding ProteinsRyanodine Receptor Calcium Release ChannelU2SURP protein, human

Identifiers

PMID23148228
PMCPMC3537033
OpenAlexW2044459945

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.