Evidence map›Paper›PMID 41965334›Full record

ArticleNature communications2026

VGLL4-driven TEAD4 multimerization orchestrates DNA binding and YAP recruitment.

Zhiyun Ren, Yilin Zhao, Wentao Yu, Xia Zhang, Xiaoxuan Song, Yanling Bao, Meng Hu, Lishuang Chen, Hao Yang, Bingkai Cheng and 4 more

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

14 authors.

Zhiyun Ren *School of Life Science and Technology, ShanghaiTech University, Shanghai, China.
Yilin Zhao *School of Life Science and Technology, ShanghaiTech University, Shanghai, China.
Wentao YuState Key Laboratory of Cell Biology, Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, Shanghai, China.
Xia ZhangSchool of Life Science and Technology, ShanghaiTech University, Shanghai, China.
Xiaoxuan SongSchool of Life Science and Technology, ShanghaiTech University, Shanghai, China.
Yanling BaoSchool of Life Science and Technology, ShanghaiTech University, Shanghai, China.
Meng HuSchool of Life Science and Technology, ShanghaiTech University, Shanghai, China.
Lishuang ChenSchool of Life Science and Technology, ShanghaiTech University, Shanghai, China.
Hao YangSheng Yushou Center of Cell Biology and Immunology, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Bingkai ChengSchool of Life Science and Technology, ShanghaiTech University, Shanghai, China.
Cong LiuInterdisciplinary Research Center on Biology and Chemistry, State Key Laboratory of Chemical Biology, Shanghai Academy of Natural Sciences (SANS), Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, China.ORCID http://orcid.org/0000-0003-3425-6672
Yunyun JinSheng Yushou Center of Cell Biology and Immunology, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China. yunyunjin@sjtu.edu.cn.ORCID http://orcid.org/0000-0003-1353-8697
Lei ZhangSchool of Life Science and Technology, ShanghaiTech University, Shanghai, China. rayzhang@sjtu.edu.cn.ORCID http://orcid.org/0009-0007-3328-597X
Bo SunSchool of Life Science and Technology, ShanghaiTech University, Shanghai, China. sunbo@shanghaitech.edu.cn.ORCID http://orcid.org/0000-0002-4590-7795

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Hippo pathway, a highly conserved kinase signaling cascade, is central to regulating cell growth and proliferation, tissue homeostasis, and organ development. As downstream effectors of this pathway, TEAD1-4 proteins serve as sequence-specific transcription factors in mammals. They collaborate with cofactors, such as VGLL and YAP/TAZ, to modulate gene expression, thereby controlling diverse cellular processes. Here, employing fluorescence-combined optical tweezers, we demonstrate that monomeric TEAD4 binds to consensus motifs with association rates significantly higher than nonspecific DNA, while the dissociation rates are fast and comparable. Yet, TEAD4, through multimerization, gains multiple DNA binding sites, supporting elongated DNA residence time and YAP recruitment. Moreover, both YAP and VGLL4 can promote TEAD4 multimerization and strengthen its DNA binding and sequence specificity. Unexpectedly, the presence of two Tondu domains in VGLL4 elicits a stoichiometry-dependent effect on YAP recruitment to DNA-bound TEAD4: A low VGLL4:TEAD4 molar ratio enhances this process, whereas a high ratio inhibits it. These findings offer a dynamic understanding of how a eukaryotic TF interacts with DNA and underscore a distinct molecular mechanism by which VGLL4 modulates TEAD4-mediated YAP recruitment in the Hippo pathway.

Indexed as

Adaptor Proteins, Signal TransducingDNADNA-Binding ProteinsMuscle ProteinsTranscription FactorsAnimalsBinding SitesHEK293 CellsHumansProtein BindingProtein MultimerizationTEA Domain Transcription FactorsYAP-Signaling ProteinsAdaptor Proteins, Signal TransducingDNADNA-Binding ProteinsMuscle ProteinsTEAD4 protein, humanTEA Domain Transcription FactorsTranscription FactorsVGLL4 protein, humanYAP-Signaling Proteins

Identifiers

PMID41965334
PMCPMC13247214

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.