Evidence map›Paper›PMID 23791819›Full record

ArticleDevelopmental biology2013

Dvr1 transfers left-right asymmetric signals from Kupffer's vesicle to lateral plate mesoderm in zebrafish.

Annita G Peterson, Xinghao Wang, H Joseph Yost

Abstract read
In one paragraph

Article in Developmental biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. Review
  3. Getting to the Heart of Left-Right Asymmetry: Contributions from the Zebrafish Model.Journal of cardiovascular development and disease · 2021
    Review
  4. Article
  5. Article
  6. Article
  7. TGF-β Family Signaling in Early Vertebrate Development.Cold Spring Harbor perspectives in biology · 2018
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Molecular specification of germ layers in vertebrate embryos.Cellular and molecular life sciences : CMLS · 2016
    Review
  14. Article
  15. Left-right asymmetry: lessons from Cancún.Development (Cambridge, England) · 2013
    Article
  16. 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

3 authors.

Annita G PetersonDepartment of Neurobiology and Anatomy, University of Utah Molecular Medicine Program, Salt Lake City, UT 84112, USA.
Xinghao Wang
H Joseph Yost

Funding

Genome-wide Analysis of Cardiac Development in ZebrafishU01HL098160 · NHLBI · UNIVERSITY OF UTAH · PI YOST, H. JOSEPH · 2009 to 2014
$8.0M
Genetic regulation of left-right organ discordanceR01HL066292 · NHLBI · UNIVERSITY OF UTAH · PI YOST, H. JOSEPH · 2001 to 2009
$3.0M
REGULATION AND INTERACTION OF CYTOCHROMES P-450 IN LIVER MICROSOMESZ01HL000981 · NHLBI · HEART, LUNG, AND BLOOD INSTITUTE · PI NAGATA, K · 1985 to 1986
–
NHLBI NIH HHS R01 HL066292NHLBI NIH HHS R01HL66292NHLBI NIH HHS U01HL0981NHLBI NIH HHS U01 HL098160
6 · The paper itself

Abstract

An early step in establishing left-right (LR) symmetry in zebrafish is the generation of asymmetric fluid flow by Kupffer's vesicle (KV). As a result of fluid flow, a signal is generated and propagated from the KV to the left lateral plate mesoderm, activating a transcriptional response of Nodal expression in the left lateral plate mesoderm (LPM). The mechanisms and molecules that aid in this transfer of information from the KV to the left LPM are still not clear. Here we provide several lines of evidence demonstrating a role for a member of the TGFβ family member, Dvr1, a zebrafish Vg1 ortholog. Dvr1 is expressed bilaterally between the KV and the LPM. Knockdown of Dvr1 by morpholino causes dramatically reduced or absent expression of southpaw (spaw, a Nodal homolog), in LPM, and corresponding loss of downstream Lefty (lft1 and lft) expression, and aberrant brain and heart LR patterning. Dvr1 morphant embryos have normal KV morphology and function, normal expression of southpaw (spaw) and charon (cha) in the peri-KV region and normal expression of a variety of LPM markers in LPM. Additionally, Dvr1 knockdown does not alter the capability of LPM to respond to signals that initiate and propagate spaw expression. Co-injection experiments in Xenopus and zebrafish indicate that Dvr1 and Spaw can enhance each other's ability to activate the Nodal response pathway and co-immunoprecipitation experiments reveal differential relationships among activators and inhibitors in this pathway. These results indicate that Dvr1 is responsible for enabling the transfer of a left-right signal from KV to the LPM.

Indexed as

Body PatterningSignal TransductionAnimalsAnimal StructuresCiliaEmbryo, NonmammalianGene Expression Regulation, DevelopmentalGene Knockdown TechniquesImmunoprecipitationMesodermMiceModels, BiologicalMorpholinosRNA, MessengerTransforming Growth Factor betaXenopusGdf3 protein, zebrafishMorpholinosRNA, MessengerTransforming Growth Factor betaZebrafish ProteinsAxis formationCell signalingLeft–rightNodalVg1Zebrafish

Identifiers

PMID23791819
PMCPMC3888838

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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.