Evidence map›Paper›PMID 42371315›Full record

ArticleGenes & genomics2026

BMP/Ventx1.1 axis modulates the multiciliogenesis in the early Xenopus epidermis.

Neha Kaushik, Zia Ur Rehman, Soochul Park, Seung-Hwan Lee, Unjoo Lee, Jaebong Kim

Abstract read
PubMed Publisher
In one paragraph

Article in Genes & genomics, 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.

Neha KaushikDepartment of Biochemistry, Institute of Cell Differentiation and Ageing, College of Medicine, Hallym University, Chuncheon, Gangwon-Do, 24252, Republic of Korea.ORCID http://orcid.org/0009-0001-7369-2744
Zia Ur RehmanDepartment of Neuroscience, Johns Hopkins University, Baltimore, MD, 21218, USA.ORCID http://orcid.org/0000-0003-0998-0116
Soochul ParkDepartment of Biological Sciences, Sookmyung Women's University, Seoul, 04310, South Korea.ORCID http://orcid.org/0000-0002-7029-3414
Seung-Hwan LeeDepartment of Biochemistry, Institute of Cell Differentiation and Ageing, College of Medicine, Hallym University, Chuncheon, Gangwon-Do, 24252, Republic of Korea.ORCID https://orcid.org/0000-0002-2017-5671
Unjoo LeeDivision of Software, Hallym University, Chuncheon, 24252, Korea. ejlee@hallym.ac.kr.ORCID http://orcid.org/0000-0002-2405-5538
Jaebong KimDepartment of Biochemistry, Institute of Cell Differentiation and Ageing, College of Medicine, Hallym University, Chuncheon, Gangwon-Do, 24252, Republic of Korea. jbkim@hallym.ac.kr.ORCID http://orcid.org/0000-0003-1609-338X

Funding

Basic Science Research funded by Korean Government RS202300240976Ministry of Education and National Research Foundation of Korea GLOCAL-202406270001National Research Foundation of Korea RS-2021-NR057660National Research Foundation of Korea RS-2022-NR070033
6 · The paper itself

Abstract

backgroundIn Xenopus laevis, multiciliated cells (MCCs) in epidermis produce coordinated motile cilia to promote fluid flow across epithelial surfaces. In a previous study, it has been reported that Bmp signaling negatively regulates the multiciliated cell formation. However, Bmp signaling is required for the early ectodermal patterning and epidermal specification.

objectiveIn the present study, the requirement of Bmp signaling was examined in ectoderm specification including multiciliogenesis of epidermis. Inhibition of Bmp signaling using a dominant-negative Bmp receptor (Dnbr) decreased MCC formation both in animal cap explants and whole embryos.

methodsDifferentially expressed MCC-associated transcripts were confirmed by transcriptome and RT-qPCR analysis of Bmp-inhibited and control animal cap explants. The promoters of multicilia-associated genes including mcidas, foxj1, deup1 and ccno were cloned to examine how Bmp signaling regulated MCC gene expression.

resultsDnbr-injected embryos consistently showed the reduced promoter activity. However, a direct target gene of Bmp signaling ventx1.1 restored MCC gene expression and promoter activity as well as epidermal marker expression in Dnbr-injected embryos.

conclusionTogether, the results support a model in which early BMP/Ventx1.1 axis positively modulates epidermal multiciliogenesis at least in part by establishing epidermal competence through ventx1.1 associated transcriptional programs.

Indexed as

Bone Morphogenetic ProteinsEpidermisHomeodomain ProteinsXenopus laevisXenopus ProteinsAnimalsCiliaGene Expression Regulation, DevelopmentalPromoter Regions, GeneticSignal TransductionBone Morphogenetic ProteinsHomeodomain ProteinsXenopus ProteinsBmp signalingCcnodeup1foxj1McidasMulticiliated cellsMulticiliogenesisventx1.1

Identifiers

What OpenQuestion holds

Textmetadata
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.