Evidence map›Paper›PMID 38877839›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2024

The dishevelled associated activator of morphogenesis protein 2 (Daam2) regulates neural tube closure.

Kaushik Nama, Baihao Su, Jonathan Marquez, Mustafa K Khokha, Raymond Habas

Abstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Kaushik NamaDepartment of Biology, Temple University, Philadelphia, Pennsylvania, USA.
Baihao SuDepartment of Biology, Temple University, Philadelphia, Pennsylvania, USA.
Jonathan MarquezPediatric Genomics Discovery Program, Department of Pediatrics and Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.
Mustafa K KhokhaPediatric Genomics Discovery Program, Department of Pediatrics and Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.
Raymond HabasDepartment of Biology, Temple University, Philadelphia, Pennsylvania, USA.ORCID 0000-0003-4804-4128

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Non-canonical Wnt signaling and cell motilityR01GM078172 · NIGMS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI HABAS, RAYMOND · 2007 to 2018
$3.1M
A system approach to the analysis of Heterotaxy Candidate GenesR01HD102186 · NICHD · YALE UNIVERSITY · PI KHOKHA, MUSTAFA K · 2020 to 2024
$3.1M
Characterization of two proteins that regulate vertebrateR03HD107523 · NICHD · TEMPLE UNIV OF THE COMMONWEALTH · PI HABAS, RAYMOND · 2022 to 2023
$155k
Eunice Kennedy Shriver National Institute of Child Health and Human Development HD102186Eunice Kennedy Shriver National Institute of Child Health and Human Development HD107523NCATS NIH HHS UL1 TR001863NICHD NIH HHS R01 HD102186NICHD NIH HHS R03 HD107523NIGMS NIH HHS GM078172NIGMS NIH HHS R01 GM078172
6 · The paper itself

Abstract

backgroundThe Wnt signaling pathway is highly conserved in metazoans and regulates a large array of cellular processes including motility, polarity and fate determination, and stem cell homeostasis. Modulation of the actin cytoskeleton via the non-canonical Wnt pathway regulate cell polarity and cell migration that are required for proper vertebrate gastrulation and subsequent neurulation. However, the mechanism(s) of how the non-canonical pathway mediates actin cytoskeleton modulation is not fully understood.

resultsHerein, we characterize the role of the Formin-homology protein; dishevelled associated activator of morphogenesis 2 (Daam2) protein in the Wnt signaling pathway. Co-immunoprecipitation assays confirm the binding of Daam2 to dishevelled2 (Dvl2) as well as the domains within these proteins required for interaction; additionally, the interaction between Daam2 and Dvl2 was Wnt-regulated. Sub-cellular localization studies reveal Daam2 is cytoplasmic and regulates the cellular actin cytoskeleton by modulating actin filament formation. During Xenopus development, a knockdown or loss of Daam2 specifically produces neural tube closure defects indicative of a role in non-canonical signaling. Additionally, our studies did not identify any role for Daam2 in canonical Wnt signaling in mammalian culture cells or the Xenopus embryo.

conclusionsOur studies together identify Daam2 as a component of the non-canonical Wnt pathway and Daam2 is a regulator of neural tube morphogenesis during vertebrate development.

Indexed as

Dishevelled ProteinsNeural TubeWnt Signaling PathwayXenopus ProteinsActin CytoskeletonAdaptor Proteins, Signal TransducingAnimalsHumansNeurulationXenopus laevisAdaptor Proteins, Signal TransducingDishevelled ProteinsXenopus Proteinsgastrulationneural tube closureWntXenopus

Identifiers

PMID38877839
PMCPMC11611695

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Registered trials

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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.