Evidence map›Paper›PMID 28689737›Full record

ArticleDevelopmental biology2017

Asymmetrically deployed actomyosin-based contractility generates a boundary between developing leg segments in Drosophila.

Dan Ly, Erin Resch, George Ordiway, Stephen DiNardo

Abstract read
In one paragraph

Article in Developmental biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
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

4 authors.

Dan LyDepartment of Cell and Developmental Biology, Perelman School of Medicine, the University of Pennsylvania, Philadelphia, PA 19104, United States.
Erin ReschDepartment of Cell and Developmental Biology, Perelman School of Medicine, the University of Pennsylvania, Philadelphia, PA 19104, United States.
George OrdiwayDepartment of Cell and Developmental Biology, Perelman School of Medicine, the University of Pennsylvania, Philadelphia, PA 19104, United States.
Stephen DiNardoDepartment of Cell and Developmental Biology, Perelman School of Medicine, the University of Pennsylvania, Philadelphia, PA 19104, United States.

Funding

Stem Cell Renewal And Differentiation in SpermatogenesisR01GM060804 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI DINARDO, STEPHEN FRANCIS · 1999 to 2019
$6.7M
PATTERNING: THE CELL BIOLOGY OF DEVELOPMENTAL SIGNALINGR01GM045747 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI DINARDO, STEPHEN FRANCIS · 1992 to 2013
$3.6M
NIGMS NIH HHS R01 GM045747NIGMS NIH HHS R01 GM060804
6 · The paper itself

Abstract

The formation of complex tissues from simple epithelial sheets requires the regional subdivision of the developing tissue. This is initially accomplished by a sequence of gene regulatory hierarchies that set up distinct fates within adjacent territories, and rely on cross-regulatory interactions to do so. However, once adjacent territories are established, cells that confront one another across territorial boundaries must actively participate in maintaining separation from each other. Classically, it was assumed that adhesive differences would be a primary means of sorting cells to their respective territories. Yet it is becoming clear that no single, simple mechanism is at play. In the few instances studied, an emergent theme along developmental boundaries is the generation of asymmetry in cell mechanical properties. The repertoire of ways in which cells might establish and then put mechanical asymmetry to work is not fully appreciated since only a few boundaries have been molecularly studied. Here, we characterize once such boundary in the develop leg epithelium of Drosophila. The region of the pretarsus / tarsus is a known gene expression boundary that also exhibits a lineage restriction (Sakurai et al., 2007). We now show that the interface comprising this boundary is strikingly aligned compared to other cell interfaces across the disk. The boundary also exhibits an asymmetry for both Myosin II accumulation as well as one of its activators, Rho Kinase. Furthermore, the enrichment correlates with increased mechanical tension across that interface, and that tension is Rho Kinase-dependent. Lastly, interfering with actomyosin contractility, either by depletion of myosin heavy chain or expression of a phosphomimetic variant of regulatory light chain causes defects in alignment of the interfaces. These data suggest strongly that mechanical asymmetries are key in establishing and maintaining this developmental boundary.

Indexed as

ActomyosinAnimalsBody PatterningDrosophila melanogasterDrosophila ProteinsExtremitiesrho-Associated KinasesActomyosinDrosophila Proteinsrho-Associated Kinases

Identifiers

PMID28689737
PMCPMC5577936

What OpenQuestion holds

Textmetadata
LicenceTDM
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.