Evidence map›Paper›PMID 39882855›Full record

ArticleeLife2025

Myristoylated Neuronal Calcium Sensor-1 captures the preciliary vesicle at distal appendages.

Tomoharu Kanie, Roy Ng, Keene L Abbott, Niaj Mohammad Tanvir, Esben Lorentzen, Olaf Pongs, Peter K Jackson

Abstract read
In one paragraph

Article in eLife, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
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  4. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Tomoharu KanieBaxter Laboratory, Department of Microbiology & Immunology and Department of Pathology, Stanford University, Stanford, United States.ORCID https://orcid.org/0000-0002-2084-1451
Roy NgBaxter Laboratory, Department of Microbiology & Immunology and Department of Pathology, Stanford University, Stanford, United States.
Keene L AbbottBaxter Laboratory, Department of Microbiology & Immunology and Department of Pathology, Stanford University, Stanford, United States.ORCID https://orcid.org/0000-0002-6166-704X
Niaj Mohammad TanvirDepartment of Molecular Biology and Genetics, Aarhus University, Aarhus, Denmark.
Esben LorentzenDepartment of Molecular Biology and Genetics, Aarhus University, Aarhus, Denmark.ORCID https://orcid.org/0000-0001-6493-7220
Olaf PongsInstitute for Physiology, Center for Integrative Physiology and Molecular Medicine, Saarland University, Saarbrücken, Germany.
Peter K JacksonBaxter Laboratory, Department of Microbiology & Immunology and Department of Pathology, Stanford University, Stanford, United States.

Funding

Proteomics CoreP20GM103447 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Mark L Lang · 2012 to 2026
$60.2M
Tissue Pathology Shared ResourceP30CA225520 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Wade Williams · 2018 to 2026
$27.1M
TUMOR RESISTANCE MECHANISMS TO ANTI-VEGF THERAPY IN PROSTATE CANCER (Sukyung Woo)P20GM103639 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI DHANASEKARAN, DANNY N. · 2012 to 2022
$21.3M
Mechanisms of Ciliary Signaling Controlling Obesity and Metabolic DiseaseR01GM121565 · NIGMS · STANFORD UNIVERSITY · PI JACKSON, PETER KENT · 2017 to 2025
$4.3M
Centriolar-ciliary signaling mechanisms in tissue regeneration and differentiationR01GM114276 · NIGMS · STANFORD UNIVERSITY · PI JACKSON, PETER KENT · 2015 to 2018
$1.5M
Understanding the molecular mechanisms of cilia formationR35GM151013 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Tomoharu Kanie · 2023 to 2026
$1.4M
OneView 4kX4k sCMOS camera for transmission electron microscopy applicationsS10OD028536 · OD · STANFORD UNIVERSITY · PI MULHOLLAND, JONATHAN W · 2020 to 2020
$195k
NCI NIH HHS P30 CA225520NIGMS NIH HHS 1R35GM151013NIGMS NIH HHS P20 GM103447NIGMS NIH HHS P20GM103447NIGMS NIH HHS P20 GM103639NIGMS NIH HHS R01 GM114276NIGMS NIH HHS R01GM114276NIGMS NIH HHS R01 GM121565NIGMS NIH HHS R01GM121565NIGMS NIH HHS R35 GM151013NIH HHS S10 OD028536
6 · The paper itself

Abstract

The primary cilium is a microtubule-based organelle that cycles through assembly and disassembly. In many cell types, formation of the cilium is initiated by recruitment of preciliary vesicles to the distal appendage of the mother centriole. However, the distal appendage mechanism that directly captures preciliary vesicles is yet to be identified. In an accompanying paper, we show that the distal appendage protein, CEP89, is important for the preciliary vesicle recruitment, but not for other steps of cilium formation (Kanie et al., 2025). The lack of a membrane-binding motif in CEP89 suggests that it may indirectly recruit preciliary vesicles via another binding partner. Here, we identify Neuronal Calcium Sensor-1 (NCS1) as a stoichiometric interactor of CEP89. NCS1 localizes to the position between CEP89 and the centriole-associated vesicle marker, RAB34, at the distal appendage. This localization was completely abolished in

Indexed as

CentriolesCiliaNeuronal Calcium-Sensor ProteinsNeuropeptidesAnimalsHumansNeuronsfrequenin calcium sensor proteinsNeuronal Calcium-Sensor ProteinsNeuropeptidescell biologycentrioleciliaciliary vesicleciliogenesisdistal appendagehumanintracellular vesiclemouse

Identifiers

PMID39882855
PMCPMC11984960

What OpenQuestion holds

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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.