Evidence map›Paper›PMID 27551058›Full record

ArticleThe Journal of cell biology2016

RhoA GTPase inhibition organizes contraction during epithelial morphogenesis.

Frank M Mason, Shicong Xie, Claudia G Vasquez, Michael Tworoger, Adam C Martin

Abstract read
In one paragraph

Article in The Journal of cell biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers.

0numbers the graph read from it
0cells of the map it votes in
88citing 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

88 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. An active matter model captures spatial dynamics of actomyosin oscillations in larval epithelial cells duringProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  5. Reprogramming of Human Limbal Niche Progenitors.International journal of medical sciences · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Regulation of intercellular viscosity by E-cadherin-dependent phosphorylation of EGFR in collective cell migration.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  11. Article
  12. Molecular biology of the cell · 2024
    Article
  13. Review
  14. Patterning of the cell cortex by Rho GTPases.Nature reviews. Molecular cell biology · 2024
    Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article

28 more citing papers are in PubMed but not listed here.

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

5 authors.

Frank M MasonDepartment of Biology, Massachusetts Institute of Technology, Cambridge, MA 02142.
Shicong XieComputational and Systems Biology, Massachusetts Institute of Technology, Cambridge, MA 02142.
Claudia G VasquezDepartment of Biology, Massachusetts Institute of Technology, Cambridge, MA 02142.
Michael TworogerDepartment of Biology, Massachusetts Institute of Technology, Cambridge, MA 02142.
Adam C MartinDepartment of Biology, Massachusetts Institute of Technology, Cambridge, MA 02142 acmartin@mit.edu.

Funding

Drosophila Transgenic RNAi Resource ProjectR01GM084947 · NIGMS · HARVARD MEDICAL SCHOOL · PI PERRIMON, NORBERT · 2008 to 2019
$9.8M
Graduate Training in Computational and Systems BiologyT32GM087237 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BURGE, CHRISTOPHER B · 2009 to 2023
$4.6M
NIGMS NIH HHS R01 GM084947NIGMS NIH HHS T32 GM087237
6 · The paper itself

Abstract

During morphogenesis, contraction of the actomyosin cytoskeleton within individual cells drives cell shape changes that fold tissues. Coordination of cytoskeletal contractility is mediated by regulating RhoA GTPase activity. Guanine nucleotide exchange factors (GEFs) activate and GTPase-activating proteins (GAPs) inhibit RhoA activity. Most studies of tissue folding, including apical constriction, have focused on how RhoA is activated by GEFs to promote cell contractility, with little investigation as to how GAPs may be important. Here, we identify a critical role for a RhoA GAP, Cumberland GAP (C-GAP), which coordinates with a RhoA GEF, RhoGEF2, to organize spatiotemporal contractility during Drosophila melanogaster apical constriction. C-GAP spatially restricts RhoA pathway activity to a central position in the apical cortex. RhoGEF2 pulses precede myosin, and C-GAP is required for pulsation, suggesting that contractile pulses result from RhoA activity cycling. Finally, C-GAP expression level influences the transition from reversible to irreversible cell shape change, which defines the onset of tissue shape change. Our data demonstrate that RhoA activity cycling and modulating the ratio of RhoGEF2 to C-GAP are required for tissue folding.

Indexed as

MorphogenesisAnimalsCell PolarityDrosophila melanogasterDrosophila ProteinsEmbryo, NonmammalianEnzyme ActivationEpithelial CellsGTPase-Activating ProteinsMyosinsrhoA GTP-Binding Proteinrho-Associated KinasesRho Guanine Nucleotide Exchange FactorsRNA, Small InterferingSignal TransductionDrosophila ProteinsGTPase-Activating ProteinsMyosinsrhoA GTP-Binding Proteinrho-Associated Kinasesrho GTPase-activating proteinRho Guanine Nucleotide Exchange FactorsRNA, Small Interfering

Identifiers

PMID27551058
PMCPMC5004446

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.