Evidence map›Paper›PMID 40654709›Full record

ArticlebioRxiv : the preprint server for biology2025

Proteomic profiling of primary cilia in the developing brain uncovers new regulators of cortical development.

Xiaoliang Liu, Oscar Torres Gutierrez, Gurleen Kaur, Yazan Al-Issa, Sabyasachi Baboo, Jolene K Diedrich, Eva Cai, John R Yates, Xuecai Ge

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Xiaoliang LiuDepartment of Molecular and Cell Biology, University of California, Merced, Merced California, 95340, USA.
Oscar Torres GutierrezDepartment of Molecular and Cell Biology, University of California, Merced, Merced California, 95340, USA.
Gurleen KaurDepartment of Molecular and Cell Biology, University of California, Merced, Merced California, 95340, USA.
Yazan Al-IssaDepartment of Molecular and Cell Biology, University of California, Merced, Merced California, 95340, USA.
Sabyasachi BabooDepartment of Integrative Structural & Computational Biology, The Scripps Research Institute, La Jolla, CA, United States.
Jolene K DiedrichDepartment of Integrative Structural & Computational Biology, The Scripps Research Institute, La Jolla, CA, United States.ORCID 0000-0002-4547-5160
Eva CaiDepartment of Molecular and Cell Biology, University of California, Merced, Merced California, 95340, USA.
John R YatesDepartment of Integrative Structural & Computational Biology, The Scripps Research Institute, La Jolla, CA, United States.
Xuecai GeDepartment of Molecular and Cell Biology, University of California, Merced, Merced California, 95340, USA.

Funding

TrainingP41GM103533 · NIGMS · UNIVERSITY OF WASHINGTON · PI DAVIS, TRISHA N. · 2012 to 2021
$20.7M
Regulation of the Hedgehog Pathway by new cilium proteins in Development and DiseaseR01GM143276 · NIGMS · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI GE, XUECAI · 2022 to 2025
$1.5M
Target PDE4D to inhibit the Hedgehog pathwayR15CA235749 · NCI · UNIVERSITY OF CALIFORNIA, MERCED · PI GE, XUECAI · 2019 to 2022
$795k
Mechanistic study of Hedgehog signaling in the ciliumR21CA274595 · NCI · UNIVERSITY OF CALIFORNIA, MERCED · PI GE, XUECAI · 2022 to 2022
$385k
NCI NIH HHS R15 CA235749NCI NIH HHS R21 CA274595NIGMS NIH HHS P41 GM103533NIGMS NIH HHS R01 GM143276
6 · The paper itself

Abstract

In the developing brain, the primary cilia of radial glial cells extend from the surface of the lateral ventricle, serving as the signaling hub to integrate environmental cues critical for brain formation. Dysfunctions in ciliary proteins contribute to a wide range of brain structural abnormalities in ciliopathies, yet identifying the bona fide ciliary protein components in the brain remains a significant challenge. Here, using proximity labeling and quantitative proteomics, we systematically charted proteins localized to the cilia of radial glial cells in the dorsal and ventral regions of the embryonic brain. From this dataset, we identified cohorts of new molecules intrinsic to the cilia at distinct regions of the developing brain. We validated the cilium localization of several components of the translation machinery and studied the mechanistic roles of ciliary candidates previously linked to brain malformation, including Marcks, a key regulator of radial glial polarity, and Ckap2l, a protein associated with Filippi syndrome. These results revealed previously unrecognized ciliary mechanisms that regulate brain development. Thus, our brain proteomic dataset provides a unique resource for understanding ciliary functions in brain development and the molecular etiology of developmental disorders.

Identifiers

PMID40654709
PMCPMC12247902

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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.