Evidence map›Paper›PMID 37013443›Full record

ArticleJournal of cell science2023

Calcineurin associates with centrosomes and regulates cilia length maintenance.

Eirini Tsekitsidou, Cassandra J Wong, Idil Ulengin-Talkish, Angela I M Barth, Tim Stearns, Anne-Claude Gingras, Jennifer T Wang, Martha S Cyert

Open access · hybridAbstract read
In one paragraph

Article in Journal of cell science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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  5. Article
  6. Review
  7. Article
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  11. Article
  12. A cellular atlas of calcineurin signaling.Biochimica et biophysica acta. Molecular cell research · 2023
    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

8 authors at 3 institutions in 2 countries.

Eirini TsekitsidouDepartment of Biology, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0003-0946-9254
Cassandra J WongLunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, ON, M5G 1X5, Canada.
Idil Ulengin-TalkishDepartment of Biology, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0003-2809-4603
Angela I M BarthDepartment of Biology, Stanford University, Stanford, CA 94305, USA.
Tim StearnsDepartment of Biology, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0002-0671-6582
Anne-Claude GingrasLunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, ON, M5G 1X5, Canada.ORCID 0000-0002-6090-4437
Jennifer T WangDepartment of Biology, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0002-8506-5182
Martha S CyertDepartment of Biology, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0003-3825-7437
Stanford University · USMount Sinai Hospital · CAStanford Medicine · US

Funding

Systematic elucidation of calcineurin phosphatase signaling in humansR35GM136243 · NIGMS · STANFORD UNIVERSITY · PI Martha S. Cyert · 2020 to 2026
$3.9M
Structure and mechanism of the centrosome-cilium complexR35GM130286 · NIGMS · STANFORD UNIVERSITY · PI STEARNS, TIM · 2019 to 2023
$3.4M
Molecular mechanisms of centriolar triplet microtubule formationR00GM131024 · NIGMS · WASHINGTON UNIVERSITY · PI WANG, JENNIFER TONG · 2022 to 2024
$747k
Molecular mechanisms of centriolar triplet microtubule formationK99GM131024 · NIGMS · STANFORD UNIVERSITY · PI WANG, JENNIFER TONG · 2019 to 2021
$272k
NIGMS NIH HHS K99 GM131024NIGMS NIH HHS R00 GM131024NIGMS NIH HHS R35 GM130286NIGMS NIH HHS R35 GM136243NIH HHS R35 GM136243
6 · The paper itself

Abstract

Calcineurin, or protein phosphatase 2B (PP2B), the Ca2+ and calmodulin-activated phosphatase and target of immunosuppressants, has many substrates and functions that remain uncharacterized. By combining rapid proximity-dependent labeling with cell cycle synchronization, we mapped the spatial distribution of calcineurin in different cell cycle stages. While calcineurin-proximal proteins did not vary significantly between interphase and mitosis, calcineurin consistently associated with multiple centrosomal and/or ciliary proteins. These include POC5, which binds centrins in a Ca2+-dependent manner and is a component of the luminal scaffold that stabilizes centrioles. We show that POC5 contains a calcineurin substrate motif (PxIxIT type) that mediates calcineurin binding in vivo and in vitro. Using indirect immunofluorescence and ultrastructure expansion microscopy, we demonstrate that calcineurin colocalizes with POC5 at the centriole, and further show that calcineurin inhibitors alter POC5 distribution within the centriole lumen. Our discovery that calcineurin directly associates with centriolar proteins highlights a role for Ca2+ and calcineurin signaling at these organelles. Calcineurin inhibition promotes elongation of primary cilia without affecting ciliogenesis. Thus, Ca2+ signaling within cilia includes previously unknown functions for calcineurin in maintenance of cilia length, a process that is frequently disrupted in ciliopathies.

Indexed as

CalcineurinCiliaCalciumCentriolesCentrosomeProteinsCalcineurinCalciumProteinsCalcineurinCentrioleCentrosomeCiliaPhosphatasePOC5

Identifiers

PMID37013443
PMCPMC10163345
OpenAlexW4362521579

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.