Evidence map›Paper›PMID 21750544›Full record

ArticleNature communications2011

The Wnt3a/β-catenin target gene Mesogenin1 controls the segmentation clock by activating a Notch signalling program.

Ravindra B Chalamalasetty, William C Dunty, Kristin K Biris, Rieko Ajima, Michelina Iacovino, Arica Beisaw, Lionel Feigenbaum, Deborah L Chapman, Jeong Kyo Yoon, Michael Kyba and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Nature communications, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

44 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Time and space in segmentation.Interface focus · 2021
    Article
  10. eLife · 2020
    Article
  11. Article
  12. Review
  13. Review
  14. Development (Cambridge, England) · 2019
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Myogenic progenitor specification from pluripotent stem cells.Seminars in cell & developmental biology · 2017
    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

11 authors at 6 institutions in 1 country.

Ravindra B ChalamalasettyCancer and Developmental Biology Laboratory, Center for Cancer Research, National Cancer Institute-Frederick, NIH, Frederick, Maryland 21702, USA.
William C Dunty
Kristin K Biris
Rieko Ajima
Michelina Iacovino
Arica Beisaw
Lionel Feigenbaum
Deborah L Chapman
Jeong Kyo Yoon
Michael Kyba
Terry P Yamaguchi
National Cancer Institute · USFrederick National Laboratory for Cancer Research · USUniversity of Minnesota · USCenter for Cancer Research · USMaine Medical Center Research Institute · USUniversity of Pittsburgh · US

Funding

The Role of Wnt Genes in Vertebrate Development and CancerZIABC010345 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI YAMAGUCHI, TERENCE · 2009 to 2025
$23.3M
Probing the Hematopoietic Hox CodeR01HL081186 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI KYBA, MICHAEL · 2007 to 2011
$2.1M
Regulatory role and signaling mechanism of R-spondin in craniofacial developmentR01AR055278 · NIAMS · MAINEHEALTH · PI YOON, JEONG K · 2008 to 2012
$1.6M
The Role of Wnt Genes in Vertebrate Gastrointestinal DevZ01BC010345 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI YAMAGUCHI, TERENCE · 2000 to 2008
$1.2M
Intramural NIH HHS Z01 BC010345Intramural NIH HHS ZIA BC010345NIAMS NIH HHS R01 AR055278
6 · The paper itself

Abstract

Segmentation is an organizing principle of body plans. The segmentation clock, a molecular oscillator best illustrated by the cyclic expression of Notch signalling genes, controls the periodic cleavage of somites from unsegmented presomitic mesoderm during vertebrate segmentation. Wnt3a controls the spatiotemporal expression of cyclic Notch genes; however, the underlying mechanisms remain obscure. Here we show by transcriptional profiling of Wnt3a (-/-) embryos that the bHLH transcription factor, Mesogenin1 (Msgn1), is a direct target gene of Wnt3a. To identify Msgn1 targets, we conducted genome-wide studies of Msgn1 activity in embryonic stem cells. We show that Msgn1 is a major transcriptional activator of a Notch signalling program and synergizes with Notch to trigger clock gene expression. Msgn1 also indirectly regulates cyclic genes in the Fgf and Wnt pathways. Thus, Msgn1 is a central component of a transcriptional cascade that translates a spatial Wnt3a gradient into a temporal pattern of clock gene expression.

Indexed as

AnimalsBasic Helix-Loop-Helix Proteinsbeta CateninBiological ClocksBody PatterningCell DifferentiationChromatin ImmunoprecipitationElectrophoretic Mobility Shift AssayEmbryonic Stem CellsGene Expression ProfilingIn Situ HybridizationMiceMice, TransgenicReceptors, NotchReverse Transcriptase Polymerase Chain ReactionSignal TransductionBasic Helix-Loop-Helix Proteinsbeta CateninMsgn1 protein, mouseReceptors, NotchWnt3A ProteinWnt3a protein, mouseWnt3 ProteinWnt Proteins

Identifiers

PMID21750544
PMCPMC3622708
OpenAlexW1964973808

What OpenQuestion holds

Textmetadata
LicenceTDM
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.