Evidence map›Paper›PMID 39882846›Full record

ArticleeLife2025

A hierarchical pathway for assembly of the distal appendages that organize primary cilia.

Tomoharu Kanie, Beibei Liu, Julia F Love, Saxton D Fisher, Anna-Karin Gustavsson, 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 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 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
Beibei LiuDepartment of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, United States.
Julia F LoveDepartment of Chemistry, Rice University, Houston, United States.ORCID https://orcid.org/0000-0001-6642-6301
Saxton D FisherDepartment of Chemistry, Rice University, Houston, United States.
Anna-Karin GustavssonDepartment of Chemistry, Rice University, Houston, United States.ORCID https://orcid.org/0000-0002-0980-1168
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
Molecular mechanisms in the mammalian cell nucleusR35GM155365 · NIGMS · RICE UNIVERSITY · PI Anna Karin Eva Gustavsson · 2024 to 2026
$1.1M
Three-dimensional super-resolution imaging and tracking of disease and treatment mechanisms of progeriaR00GM134187 · NIGMS · RICE UNIVERSITY · PI GUSTAVSSON, ANNA KARIN EVA · 2021 to 2023
$747k
OneView 4kX4k sCMOS camera for transmission electron microscopy applicationsS10OD028536 · OD · STANFORD UNIVERSITY · PI MULHOLLAND, JONATHAN W · 2020 to 2020
$195k
Cancer Prevention and Research Institute of Texas RR200025NCI NIH HHS P30 CA225520NIGMS NIH HHS 1R35GM151013NIGMS NIH HHS P20 GM103447NIGMS NIH HHS P20GM103447NIGMS NIH HHS P20 GM103639NIGMS NIH HHS R00 GM134187NIGMS NIH HHS R00GM134187NIGMS NIH HHS R01 GM114276NIGMS NIH HHS R01GM114276NIGMS NIH HHS R01 GM121565NIGMS NIH HHS R01GM121565NIGMS NIH HHS R35 GM151013NIGMS NIH HHS R35 GM155365NIGMS NIH HHS R35GM155365NIH HHS S10 OD028536Welch Foundation C-2064-20210327
6 · The paper itself

Abstract

Distal appendages are ninefold symmetric blade-like structures attached to the distal end of the mother centriole. These structures are critical for the formation of the primary cilium, by regulating at least four critical steps: preciliary vesicle recruitment, recruitment and initiation of intraflagellar transport (IFT), and removal of CP110. While specific proteins that localize to the distal appendages have been identified, how exactly each protein functions to achieve the multiple roles of the distal appendages is poorly understood. Here, we comprehensively analyze known and newly discovered distal appendage proteins (CEP83, SCLT1, CEP164, TTBK2, FBF1, CEP89, KIZ, ANKRD26, PIDD1, LRRC45, NCS1, CEP15) for their precise localization, order of recruitment, and their roles in each step of cilia formation. Using CRISPR-Cas9 knockouts, we show that the order of the recruitment of the distal appendage proteins is highly interconnected and a more complex hierarchy. Our analysis highlights two protein modules, CEP83-SCLT1 and CEP164-TTBK2, as critical for structural assembly of distal appendages. Functional assays revealed that CEP89 selectively functions in the RAB34

Indexed as

CentriolesCiliaAnimalsCRISPR-Cas SystemsHumanscell biologycentrosomeciliaciliogenesisdistal appendagehumansuper-resolution microscopy

Identifiers

PMID39882846
PMCPMC11984956

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Registered trials

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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.