Evidence map›Paper›PMID 41820353›Full record

ArticleNature communications2026

DEUP1 functions as a scaffold for basal foot integrity and planar polarity in multiciliated cells.

Haeryung Lee, Jiyeon Lee, Miram Shin, Ravi Shankar Goutam, Jaebong Kim, Soochul Park

Abstract read
In one paragraph

Article in Nature communications, 2026. 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

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.

Haeryung Lee *Department of Biological Sciences, Sookmyung Women's University, Seoul, Korea.ORCID http://orcid.org/0000-0002-1539-9259
Jiyeon Lee *Department of Biological Sciences, Sookmyung Women's University, Seoul, Korea.
Miram Shin *Department of Biological Sciences, Sookmyung Women's University, Seoul, Korea.
Ravi Shankar GoutamDepartment of Biochemistry, Institute of Cell Differentiation and Aging, College of Medicine, Hallym University, Chuncheon, Korea.
Jaebong KimDepartment of Biochemistry, Institute of Cell Differentiation and Aging, College of Medicine, Hallym University, Chuncheon, Korea.
Soochul ParkDepartment of Biological Sciences, Sookmyung Women's University, Seoul, Korea. scpark@sookmyung.ac.kr.ORCID http://orcid.org/0000-0002-7029-3414

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiciliated cells generate numerous centrioles to support motile cilia essential for fluid flow. This process was thought to rely on the deuterosome, a DEUP1-dependent structure. Here, we show that DEUP1 plays a critical role in the basal foot (BF)-an asymmetric appendage of the basal body required for coordinated ciliary beating. Using high-resolution imaging, we localize DEUP1 to the middle tier of the BF, adjacent to CNTRL. In DEUP1 knockout mice, BF architecture is disrupted, leading to loss of rotational planar polarity, reduced cerebrospinal fluid flow, and ciliary degeneration with age. These defects are recapitulated in Xenopus epidermis, demonstrating evolutionary conservation. Notably, DEUP1 loss alone does not affect basal body or cilia number during early or mature adult stages, with overt degeneration emerging only in aged animals. Together, these findings establish DEUP1 as a key structural regulator of BF integrity that is required for the long-term maintenance of coordinated ciliary motility.

Indexed as

Basal BodiesCell PolarityCiliaAnimalsCentriolesMiceMice, KnockoutTumor Suppressor ProteinsTg737Rpw protein, mouseTumor Suppressor Proteins

Identifiers

PMID41820353
PMCPMC13125657

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.