Evidence map›Paper›PMID 26488501›Full record

ArticlePLoS genetics2015

Quantitative Differences in Nuclear β-catenin and TCF Pattern Embryonic Cells in C. elegans.

Amanda L Zacharias, Travis Walton, Elicia Preston, John Isaac Murray

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

26 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
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  12. Review
  13. Delineating the mechanisms and design principles ofComputational and structural biotechnology journal · 2022
    Review
  14. Article
  15. Article
  16. Dual Effects of Non-Coding RNAs (ncRNAs) in Cancer Stem Cell Biology.International journal of molecular sciences · 2020
    Review
  17. Article
  18. Article
  19. Article
  20. Article
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

4 authors at 1 institution in 1 country.

Amanda L ZachariasDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
Travis WaltonDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
Elicia PrestonDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
John Isaac MurrayDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
University of Pennsylvania · US

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
TRAINING PROGRAM IN DEVELOPMENTAL BIOLOGYT32HD007516 · NICHD · UNIVERSITY OF PENNSYLVANIA · PI RAPER, JONATHAN A · 1998 to 2012
$5.6M
Mechanisms integrating lineage history with fate specification in C. elegansR01GM105676 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI MURRAY, JOHN ISAAC · 2013 to 2017
$1.5M
Mechanisms governing context-dependent Wnt activity in C. elegans embryogenesisR00GM111825 · NIGMS · CINCINNATI CHILDRENS HOSP MED CTR · PI ZACHARIAS, AMANDA LUCILLE · 2018 to 2020
$747k
Dissecting the Regulation of Gene Expression during C. elegans EmbryogenesisR00GM083145 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI MURRAY, JOHN ISAAC · 2010 to 2012
$742k
Dissecting the Regulation of Gene Expression during C. elegans EmbryogenesisK99GM083145 · NIGMS · UNIVERSITY OF WASHINGTON · PI MURRAY, JOHN ISAAC · 2008 to 2009
$175k
Mechanisms governing context-dependent Wnt activity in C. elegans embryogenesisK99GM111825 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI ZACHARIAS, AMANDA LUCILLE · 2014 to 2015
$146k
NICHD NIH HHS HD007516NICHD NIH HHS T32 HD007516NIGMS NIH HHS GM083145NIGMS NIH HHS GM105676NIGMS NIH HHS GM111825NIGMS NIH HHS K99 GM083145NIGMS NIH HHS K99 GM111825NIGMS NIH HHS R00 GM083145NIGMS NIH HHS R00 GM111825NIGMS NIH HHS R01 GM105676NIH HHS P40 OD010440
6 · The paper itself

Abstract

The Wnt signaling pathway plays a conserved role during animal development in transcriptional regulation of distinct targets in different developmental contexts but it remains unclear whether quantitative differences in the nuclear localization of effector proteins TCF and β-catenin contribute to context-specific regulation. We investigated this question in Caenorhabditis elegans embryos by quantifying nuclear localization of fluorescently tagged SYS-1/β-catenin and POP-1/TCF and expression of Wnt ligands at cellular resolution by time-lapse microscopy and automated lineage tracing. We identified reproducible, quantitative differences that generate a subset of Wnt-signaled cells with a significantly higher nuclear concentration of the TCF/β-catenin activating complex. Specifically, β-catenin and TCF are preferentially enriched in nuclei of daughter cells whose parents also had high nuclear levels of that protein, a pattern that could influence developmental gene expression. Consistent with this, we found that expression of synthetic reporters of POP-1-dependent activation is biased towards cells that had high nuclear SYS-1 in consecutive divisions. We identified new genes whose embryonic expression patterns depend on pop-1. Most of these require POP-1 for either transcriptional activation or repression, and targets requiring POP-1 for activation are more likely to be expressed in the cells with high nuclear SYS-1 in consecutive divisions than those requiring POP-1 for repression. Taken together, these results indicate that SYS-1 and POP-1 levels are influenced by the parent cell's SYS-1/POP-1 levels and this may provide an additional mechanism by which POP-1 regulates distinct targets in different developmental contexts.

Indexed as

Animalsbeta CateninBody PatterningCaenorhabditis elegansCaenorhabditis elegans ProteinsCell NucleusDNA-Binding ProteinsGene Expression Regulation, DevelopmentalHigh Mobility Group ProteinsTCF Transcription FactorsTranscription FactorsWnt Signaling Pathwaybeta CateninCaenorhabditis elegans ProteinsDNA-Binding ProteinsHigh Mobility Group Proteinspop-1 protein, C elegansSys-1 protein, C elegansTCF Transcription FactorsTranscription Factors

Identifiers

PMID26488501
PMCPMC4619327
OpenAlexW2118778163

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.