Evidence map›Paper›PMID 26160902›Full record

ArticleDevelopment (Cambridge, England)2015

Dachsous1b cadherin regulates actin and microtubule cytoskeleton during early zebrafish embryogenesis.

Nanbing Li-Villarreal, Meredyth M Forbes, Andrew J Loza, Jiakun Chen, Taylur Ma, Kathryn Helde, Cecilia B Moens, Jimann Shin, Atsushi Sawada, Anna E Hindes and 5 more

RetractedErratum issuedAbstract read
In one paragraph

Article in Development (Cambridge, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

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  12. Light-sheet fluorescence microscopy for theBiomedical optics express · 2021
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Nanbing Li-VillarrealDepartment of Developmental Biology, Washington University School of Medicine in St. Louis, St. Louis, MO 63110, USA.
Meredyth M ForbesDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Yeshiva University, Bronx, NY 10461, USA.
Andrew J LozaDepartment of Internal Medicine, Washington University School of Medicine in St. Louis, St. Louis, MO 63110, USA.
Jiakun ChenDepartment of Developmental Biology, Washington University School of Medicine in St. Louis, St. Louis, MO 63110, USA.
Taylur MaDivision of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle,  WA 98109, USA.
Kathryn HeldeDivision of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle,  WA 98109, USA.
Cecilia B MoensDivision of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle,  WA 98109, USA.
Jimann ShinDepartment of Developmental Biology, Washington University School of Medicine in St. Louis, St. Louis, MO 63110, USA.
Atsushi SawadaDepartment of Developmental Biology, Washington University School of Medicine in St. Louis, St. Louis, MO 63110, USA.
Anna E HindesDepartment of Developmental Biology, Washington University School of Medicine in St. Louis, St. Louis, MO 63110, USA.
Julien DubrulleDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.
Alexander F SchierDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.
Gregory D LongmoreDepartment of Internal Medicine, Washington University School of Medicine in St. Louis, St. Louis, MO 63110, USA.
Florence L MarlowDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Yeshiva University, Bronx, NY 10461, USA Department of Neuroscience, Albert Einstein College of Medicine, Yeshiva University, Bronx, NY 10461, USA.
Lilianna Solnica-KrezelDepartment of Developmental Biology, Washington University School of Medicine in St. Louis, St. Louis, MO 63110, USA solnical@wustl.edu.

Funding

TRAINING PROGRAM IN CELLULAR &MOLEC. BIOLOGY &GENETICST32GM007491 · NIGMS · YESHIVA UNIVERSITY · PI QUERY, CHARLES C · 1985 to 2021
$17.0M
Training Program in Stem Cell and Regenerative Developmental BiologyT32HD007502 · NICHD · VANDERBILT UNIVERSITY · PI WRIGHT, CHRISTOPHER V · 1997 to 2022
$5.4M
GENETIC ANALYSIS OF CONVERGENT EXTENSION IN ZEBRAFISHR01GM055101 · NIGMS · WASHINGTON UNIVERSITY · PI SOLNICAKREZEL, LILIANNA · 1997 to 2014
$4.5M
TILLING the Zebrafish Genome: A Reverse Genetic ApproachR01HG002995 · NHGRI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI MOENS, CECILIA B, POSTLETHWAIT, JOHN H. · 2003 to 2010
$3.5M
Oocyte polarity and mRNA localization in ZebrafishR01GM089979 · NIGMS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MARLOW, FLORENCE LOUISE · 2010 to 2018
$3.0M
Mechanisms of Tangential Neuron MigrationR01NS082567 · NINDS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI MOENS, CECILIA B · 2013 to 2017
$2.1M
TILLING the Zebrafish Genome: A Reverse Genetics ApproachR01HD076585 · NICHD · FRED HUTCHINSON CANCER RESEARCH CENTER · PI MOENS, CECILIA B, SOLNICAKREZEL, LILIANNA · 2012 to 2014
$1.9M
INTERDISCIPLINARY TRAINING IN MECHANOBIOLOGY FROM NM TO CMT32EB018266 · NIBIB · WASHINGTON UNIVERSITY · PI BAYLY, PHILIP V · 2014 to 2018
$987k
NHGRI NIH HHS R01 HG002995NIBIB NIH HHS T32 EB018266NICHD NIH HHS 2T32HD007502-16A1NICHD NIH HHS R01 HD076585NICHD NIH HHS T32 HD007502NIGMS NIH HHS R01 GM055101NIGMS NIH HHS R01 GM089979NIGMS NIH HHS R01GM089979NIGMS NIH HHS R01GM55101NIGMS NIH HHS T32 GM007491NIGMS NIH HHS T32-GM007491NINDS NIH HHS R01 NS082567
6 · The paper itself

Abstract

Dachsous (Dchs), an atypical cadherin, is an evolutionarily conserved regulator of planar cell polarity, tissue size and cell adhesion. In humans, DCHS1 mutations cause pleiotropic Van Maldergem syndrome. Here, we report that mutations in zebrafish dchs1b and dchs2 disrupt several aspects of embryogenesis, including gastrulation. Unexpectedly, maternal zygotic (MZ) dchs1b mutants show defects in the earliest developmental stage, egg activation, including abnormal cortical granule exocytosis (CGE), cytoplasmic segregation, cleavages and maternal mRNA translocation, in transcriptionally quiescent embryos. Later, MZdchs1b mutants exhibit altered dorsal organizer and mesendodermal gene expression, due to impaired dorsal determinant transport and Nodal signaling. Mechanistically, MZdchs1b phenotypes can be explained in part by defective actin or microtubule networks, which appear bundled in mutants. Accordingly, disruption of actin cytoskeleton in wild-type embryos phenocopied MZdchs1b mutant defects in cytoplasmic segregation and CGE, whereas interfering with microtubules in wild-type embryos impaired dorsal organizer and mesodermal gene expression without perceptible earlier phenotypes. Moreover, the bundled microtubule phenotype was partially rescued by expressing either full-length Dchs1b or its intracellular domain, suggesting that Dchs1b affects microtubules and some developmental processes independent of its known ligand Fat. Our results indicate novel roles for vertebrate Dchs in actin and microtubule cytoskeleton regulation in the unanticipated context of the single-celled embryo.

Indexed as

ActinsAnimalsCadherinsCytoskeletonDNA PrimersExocytosisFemaleImmunohistochemistryIn Situ HybridizationMicroscopy, ConfocalMicrotubulesOptical ImagingOvaryReal-Time Polymerase Chain ReactionRNA, MessengerZebrafishActinsCadherinsDCHS1b protein, zebrafishDNA PrimersRNA, MessengerZebrafish ProteinsActinCell fatedchs1bEgg activationMicrotubuleMorphogenesis

Identifiers

PMID26160902
PMCPMC4529026

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.