Evidence map›Paper›PMID 31481532›Full record

ArticleThe Journal of cell biology2019

YAP and TAZ regulate cell volume.

Nicolas A Perez-Gonzalez, Nash D Rochman, Kai Yao, Jiaxiang Tao, Minh-Tam Tran Le, Shannon Flanary, Lucia Sablich, Ben Toler, Eliana Crentsil, Felipe Takaesu and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.7field-weighted citation impact, top 6% of its field
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

39 citing papers in PubMed, 57 citations in OpenAlex.

  1. Identification of the Down Syndrome Critical Region 3 Gene as a Mammalian Cell Size Regulator.Genes to cells : devoted to molecular & cellular mechanisms · 2026
    Article
  2. A role for theMolecular biology of the cell · 2026
    Article
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  19. Mechanosensing Piezo channels in gastrointestinal disorders.The Journal of clinical investigation · 2023
    Review
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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

21 authors at 3 institutions in 1 country.

Nicolas A Perez-Gonzalez *Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, MD.
Nash D Rochman *Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, MD.
Kai Yao *Department of Mechanical Engineering, Johns Hopkins University, Baltimore, MD.
Jiaxiang TaoDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, MD.
Minh-Tam Tran LeDepartment of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, MD.
Shannon FlanaryDepartment of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, MD.
Lucia SablichDepartment of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, MD.
Ben TolerDepartment of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, MD.
Eliana CrentsilDepartment of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, MD.
Felipe TakaesuDepartment of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, MD.
Bram LambrusDepartment of Molecular Biology and Genetics, Johns Hopkins University, School of Medicine, Baltimore, MD.
Jessie HuangDepartment of Environmental Health and Engineering, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
Vivian FuDepartment of Pharmacology and Moores Cancer Center, University of California, San Diego, La Jolla, CA.
Pragati ChengappaDepartment of Biology, Drexel University, Philadelphia, PA.ORCID 0000-0001-5763-0247
Tia M JonesDepartment of Biology, Drexel University, Philadelphia, PA.
Andrew J HollandDepartment of Molecular Biology and Genetics, Johns Hopkins University, School of Medicine, Baltimore, MD.ORCID 0000-0003-3728-6367
Steven AnDepartment of Environmental Health and Engineering, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.ORCID 0000-0003-4723-1888
Denis WirtzDepartment of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, MD.ORCID 0000-0001-6147-3045
Ryan J PetrieDepartment of Biology, Drexel University, Philadelphia, PA.ORCID 0000-0001-9780-4969
Kun-Liang GuanDepartment of Pharmacology and Moores Cancer Center, University of California, San Diego, La Jolla, CA.
Sean X SunDepartment of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, MD ssun@jhu.edu.ORCID 0000-0002-9077-7088
Johns Hopkins University · USDrexel University · USUniversity of California San Diego · US

Funding

The MARC U*STAR Program at UMBCT34GM008663 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE COUNTY · PI ROBINSON, PHYLLIS R · 1997 to 2019
$21.9M
The Role of Physical Cues in Collective Cell InvasionU54CA210173 · NCI · JOHNS HOPKINS UNIVERSITY · PI WIRTZ, DENIS · 2016 to 2020
$9.9M
T32: Predoctoral and Postdoctoral Training Program in Nanotechnology for Cancer ResearchT32CA153952 · NCI · JOHNS HOPKINS UNIVERSITY · PI Denis Wirtz · 2015 to 2026
$3.5M
Centrosome biogenesis and copy number controlR01GM114119 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI CORMACK, BRENDAN · 2015 to 2023
$3.3M
Physical mechanisms of 3D cell motilityR01GM126054 · NIGMS · DREXEL UNIVERSITY · PI PETRIE, RYAN · 2018 to 2022
$1.7M
T-32 NIH Postdoctoral Training Program in Nanotechnology for Cancer Medicine NTCMT32CA130840 · NCI · JOHNS HOPKINS UNIVERSITY · PI WIRTZ, DENIS · 2008 to 2012
$1.2M
Submicrometer silica particles for high-throughput separations of protein pharmacR01GM101464 · NIGMS · PURDUE UNIVERSITY · PI WIRTH, MARY J. · 2012 to 2015
$1.1M
NCI NIH HHS T32 CA130840NCI NIH HHS T32 CA153952NCI NIH HHS U54 CA210173NIGMS NIH HHS R01 GM101464NIGMS NIH HHS R01 GM114119NIGMS NIH HHS R01 GM126054NIGMS NIH HHS T34 GM008663
6 · The paper itself

Abstract

How mammalian cells regulate their physical size is currently poorly understood, in part due to the difficulty in accurately quantifying cell volume in a high-throughput manner. Here, using the fluorescence exclusion method, we demonstrate that the mechanosensitive transcriptional regulators YAP (Yes-associated protein) and TAZ (transcriptional coactivator with PDZ-binding motif) are regulators of single-cell volume. The role of YAP/TAZ in volume regulation must go beyond its influence on total cell cycle duration or cell shape to explain the observed changes in volume. Moreover, for our experimental conditions, volume regulation by YAP/TAZ is independent of mTOR. Instead, we find that YAP/TAZ directly impacts the cell division volume, and YAP is involved in regulating intracellular cytoplasmic pressure. Based on the idea that YAP/TAZ is a mechanosensor, we find that inhibiting myosin assembly and cell tension slows cell cycle progression from G1 to S. These results suggest that YAP/TAZ may be modulating cell volume in combination with cytoskeletal tension during cell cycle progression.

Indexed as

Cell SizeCell CycleCell Cycle ProteinsCells, CulturedCytoskeletonHEK293 CellsHumansTrans-ActivatorsTranscriptional Coactivator with PDZ-Binding Motif ProteinsTranscription FactorsCell Cycle ProteinsTrans-ActivatorsTranscriptional Coactivator with PDZ-Binding Motif ProteinsTranscription FactorsWWTR1 protein, humanYY1AP1 protein, human

Identifiers

PMID31481532
PMCPMC6781432
OpenAlexW2972027466

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.