Evidence map›Paper›PMID 10427095›Full record

ArticleThe Journal of cell biology1999

Establishment of the dorsal-ventral axis in Xenopus embryos coincides with the dorsal enrichment of dishevelled that is dependent on cortical rotation.

J R Miller, B A Rowning, C A Larabell, J A Yang-Snyder, R L Bates, R T Moon

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

84 citing papers in PubMed, 259 citations in OpenAlex.

  1. Subcellular mass spectrometry reveals proteome remodeling in an asymmetrically dividing (frog) embryonic stem cell.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. TheBiomolecules · 2025
    Review
  4. Article
  5. Article
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  7. Article
  8. Prdm15 acts upstream of Wnt4 signaling in anterior neural development ofFrontiers in cell and developmental biology · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. The developmental biology of kinesins.Developmental biology · 2021
    Review
  16. Article
  17. Single-molecule dynamics of Dishevelled at the plasma membrane and Wnt pathway activation.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  18. Article
  19. Article
  20. Review

24 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

6 authors at 3 institutions in 1 country.

J R MillerHoward Hughes Medical Institute, Department of Pharmacology, and Center for Developmental Biology, University of Washington School of Medicine, Seattle, Washington 98195, USA.
B A Rowning
C A Larabell
J A Yang-Snyder
R L Bates
R T Moon
University of Washington · USLawrence Berkeley National Laboratory · USHoward Hughes Medical Institute · US

Funding

EXPRESSION AND FUNCTIONS OF WNT GENESR01HD029360 · NICHD · UNIVERSITY OF WASHINGTON · PI MOON, RANDALL TODD · 1992 to 1996
–
NICHD NIH HHS HD29360
6 · The paper itself

Abstract

Examination of the subcellular localization of Dishevelled (Dsh) in fertilized Xenopus eggs revealed that Dsh is associated with vesicle-like organelles that are enriched on the prospective dorsal side of the embryo after cortical rotation. Dorsal enrichment of Dsh is blocked by UV irradiation of the vegetal pole, a treatment that inhibits development of dorsal cell fates, linking accumulation of Dsh and specification of dorsal cell fates. Investigation of the dynamics of Dsh localization using Dsh tagged with green fluorescent protein (Dsh-GFP) demonstrated that Dsh-GFP associates with small vesicle-like organelles that are directionally transported along the parallel array of microtubules towards the prospective dorsal side of the embryo during cortical rotation. Perturbing the assembly of the microtubule array with D(2)O, a treatment that promotes the random assembly of the array and the dorsalization of embryos, randomizes translocation of Dsh-GFP. Conversely, UV irradiation of the vegetal pole abolishes movement of Dsh-GFP. Finally, we demonstrate that overexpression of Dsh can stabilize beta-catenin in Xenopus. These data suggest that the directional translocation of Dsh along microtubules during cortical rotation and its subsequent enrichment on the prospective dorsal side of the embryo play a role in locally activating a maternal Wnt pathway responsible for establishing dorsal cell fates in Xenopus.

Indexed as

Body PatterningCell PolarityEmbryonic DevelopmentTrans-ActivatorsXenopus ProteinsAdaptor Proteins, Signal TransducingAnimalsbeta CateninBiological TransportBlastocystCell DifferentiationCytoskeletal ProteinsDeuterium OxideDishevelled ProteinsEmbryo, NonmammalianFrizzled ReceptorsAdaptor Proteins, Signal Transducingbeta CateninCtnnb1 protein, ratCTNNB1 protein, XenopusCytoskeletal ProteinsDeuterium OxideDishevelled ProteinsDVL1 protein, XenopusFrizzled ReceptorsFzd1 protein, ratFZD1 protein, XenopusNocodazolePhosphoproteinsReceptors, G-Protein-CoupledReceptors, NeurotransmitterRecombinant Fusion ProteinsTrans-ActivatorsXenopus Proteins

Identifiers

PMID10427095
PMCPMC2156185
OpenAlexW2107745042

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.