Evidence map›Paper›PMID 14657248›Full record

ArticleMolecular biology of the cell2004

Reassessing the role and dynamics of nonmuscle myosin II during furrow formation in early Drosophila embryos.

Anne Royou, Christine Field, John C Sisson, William Sullivan, Roger Karess

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 163 papers.

0numbers the graph read from it
0cells of the map it votes in
163citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

163 citing papers in PubMed, 310 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Cilia-driven epithelial folding and unfolding in an early diverging animal.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  12. Regulation of Notch signaling by non-muscle myosin II Zipper in Drosophila.Cellular and molecular life sciences : CMLS · 2024
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Evidence that tissue recoil in the earlyMolecular biology of the cell · 2023
    Article
  19. Article
  20. Article

103 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 at 3 institutions in 2 countries.

Anne RoyouCNRS Centre de Génétique Moléculaire, 91198 Gif-sur-Yvette, France.
Christine Field
John C Sisson
William Sullivan
Roger Karess
Centre National de la Recherche Scientifique · FRUniversity of California, Santa Cruz · USHarvard University · US

Funding

CYTOKINESIS IN THE EARLY DROSOPHILA EMBRYOR01GM046409 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI SULLIVAN, WILLIAM T. · 1997 to 2014
$4.7M
DROSOPHILA EMBRYONIC NUCLEAR DIVISION MUTATIONSR29GM046409 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI SULLIVAN, WILLIAM T. · 1991 to 1995
–
NIGMS NIH HHS GM46409NIGMS NIH HHS R01 GM046409
6 · The paper itself

Abstract

The early Drosophila embryo undergoes two distinct membrane invagination events believed to be mechanistically related to cytokinesis: metaphase furrow formation and cellularization. Both involve actin cytoskeleton rearrangements, and both have myosin II at or near the forming furrow. Actin and myosin are thought to provide the force driving membrane invagination; however, membrane addition is also important. We have examined the role of myosin during these events in living embryos, with a fully functional myosin regulatory light-chain-GFP chimera. We find that furrow invagination during metaphase and cellularization occurs even when myosin activity has been experimentally perturbed. In contrast, the basal closure of the cellularization furrows and the first cytokinesis after cellularization are highly dependent on myosin. Strikingly, when ingression of the cellularization furrow is experimentally inhibited by colchicine treatment, basal closure still occurs at the appropriate time, suggesting that it is regulated independently of earlier cellularization events. We have also identified a previously unrecognized reservoir of particulate myosin that is recruited basally into the invaginating furrow in a microfilament-independent and microtubule-dependent manner. We suggest that cellularization can be divided into two distinct processes: furrow ingression, driven by microtubule mediated vesicle delivery, and basal closure, which is mediated by actin/myosin based constriction.

Indexed as

ActinsAnimalsCell DivisionColchicineCytoskeletonDrosophila melanogasterDrosophila ProteinsEmbryo, NonmammalianGreen Fluorescent ProteinsLuminescent ProteinsMembrane FusionMicroscopy, ConfocalMyosin Type IIActinsColchicineDrosophila ProteinsGreen Fluorescent ProteinsLuminescent ProteinsMyosin Type II

Identifiers

PMID14657248
PMCPMC329397
OpenAlexW2142453339

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.