Evidence map›Paper›PMID 23091072›Full record

ArticleThe Journal of cell biology2012

Rbms3 functions in craniofacial development by posttranscriptionally modulating TGF-β signaling.

Chathurani S Jayasena, Marianne E Bronner

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

32 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. RNA-Binding Proteins (RBPs) and Circular RNA Biogenesis.Advances in experimental medicine and biology · 2025
    Review
  5. RNA-binding proteins regulate osteoarthritis via RNA metabolism regulation.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2024
    Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. RBMS2 inhibits the proliferation by stabilizing P21 mRNA in breast cancer.Journal of experimental & clinical cancer research : CR · 2018
    Article
  16. Article
  17. Article
  18. Shep regulatesDevelopment (Cambridge, England) · 2018
    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

2 authors at 1 institution in 1 country.

Chathurani S JayasenaDivision of Biology, California Institute of Technology, Pasadena, CA 91125, USA. csjay@caltech.edu
Marianne E Bronner
California Institute of Technology · US

Funding

Transcriptional Casualty in Embryonic Morphogenesis: from the Specifications GRNP01HD037105 · NICHD · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI MCCLAY, DAVID R · 1999 to 2018
$27.1M
Center for in Toto Genomic Analysis of Vertebrate DevelopmentP50HG004071 · NHGRI · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI FRASER, SCOTT E · 2006 to 2011
$18.4M
Evolutionary Origin of Vertebrate Neural Crest Gene NetworksR01DE017911 · NIDCR · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI BRONNER, MARIANNE · 2007 to 2011
$2.7M
NHGRI NIH HHS P50 HG004071NHGRI NIH HHS P50HG004071NICHD NIH HHS HD037105NICHD NIH HHS P01 HD037105NIDCR NIH HHS DE017911NIDCR NIH HHS R01 DE017911
6 · The paper itself

Abstract

Cranial neural crest cells form much of the facial skeleton, and abnormalities in their development lead to severe birth defects. In a novel zebrafish protein trap screen, we identified an RNA-binding protein, Rbms3, that is transiently expressed in the cytoplasm of condensing neural crest cells within the pharyngeal arches. Morphants for rbms3 displayed reduced proliferation of prechondrogenic crest and significantly altered expression for chondrogenic/osteogenic lineage markers. This phenotype strongly resembles cartilage/crest defects observed in Tgf-βr2:Wnt1-Cre mutants, which suggests a possible link with TGF-β signaling. Consistent with this are the findings that: (a) Rbms3 stabilized a reporter transcript with smad2 3' untranslated region, (b) RNA immunoprecipitation with full-length Rbms3 showed enrichment for smad2/3, and (c) pSmad2 levels were reduced in rbms3 morphants. Overall, these results suggest that Rbms3 posttranscriptionally regulates one of the major pathways that promotes chondrogenesis, the transforming growth factor β receptor (TGF-βr) pathway.

Indexed as

RNA Processing, Post-TranscriptionalAmino Acid SequenceAnimalsApoptosisBlotting, WesternCartilageCell DifferentiationCell ProliferationChondrogenesisCraniofacial AbnormalitiesEmbryo, NonmammalianFluorescent Antibody TechniqueGene Expression Regulation, DevelopmentalImmunoprecipitationIn Situ HybridizationMolecular Sequence DataReceptors, Transforming Growth Factor betaRNA-Binding ProteinsRNA, MessengerTransforming Growth Factor betaZebrafish Proteins

Identifiers

PMID23091072
PMCPMC3483135
OpenAlexW2137076204

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.