Evidence map›Paper›PMID 22710170›Full record

ReviewFEBS letters2012

Regulation of TGF-β signal transduction by mono- and deubiquitylation of Smads.

Sirio Dupont, Masafumi Inui, Stuart J Newfeld

Abstract readReview
In one paragraph

Review in FEBS letters, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Protein monoubiquitylation: targets and diverse functions.Genes to cells : devoted to molecular & cellular mechanisms · 2015
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Altered ubiquitin-proteasome signaling in right ventricular hypertrophy and failure.American journal of physiology. Heart and circulatory physiology · 2013
    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

3 authors.

Sirio DupontDepartment of Biomedical Sciences, University of Padova, Padova, Italy. dupont@bio.unipd.it
Masafumi Inui
Stuart J Newfeld

Funding

Computatonal Analysis of Gene Expression Pattern ImagesR01HG002516 · NHGRI · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI KUMAR, SUDHIR · 2003 to 2013
$5.3M
NHGRI NIH HHS HG002516NHGRI NIH HHS R01 HG002516
6 · The paper itself

Abstract

Polyubiquitylation leading to proteasomal degradation is a well-established mechanism for regulating TGF-β signal transduction components such as receptors and Smads. Recently, an equally important role was suggested for monoubiquitylation of both Smad4 and receptor-associated Smads that regulates their function without protein degradation. Monoubiquitylation of Smads was discovered following the identification of deubiquitylases required for TGF-β signaling, suggesting that continuous cycles of Smad mono- and deubiquitylation are required for proper TGF-β signal transduction. Here we summarize and discuss recent work on Smad mono- and deubiquitylation.

Indexed as

Gene Expression RegulationAnimalsEndopeptidasesHumansMiceModels, BiologicalModels, GeneticProteasome Endopeptidase ComplexSignal TransductionSmad4 ProteinTranscription FactorsTransforming Growth Factor betaUbiquitinUbiquitinationUbiquitin-Specific ProteasesUbiquitin ThiolesteraseEndopeptidasesProteasome Endopeptidase ComplexSmad4 ProteinSMAD4 protein, humanTranscription FactorsTransforming Growth Factor betaTRIM33 protein, humanUbiquitinUbiquitin-Specific ProteasesUbiquitin ThiolesteraseUSP9X protein, human

Identifiers

PMID22710170
PMCPMC3383349

What OpenQuestion holds

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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.