Evidence map›Paper›PMID 17954973›Full record

ArticleJournal of biosciences2007

Cullin4B/E3-ubiquitin ligase negatively regulates beta-catenin.

Rachana Tripathi, Satya Keerthi Kota, Usha K Srinivas

Abstract read
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In one paragraph

Article in Journal of biosciences, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

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  14. CRL4s: the CUL4-RING E3 ubiquitin ligases.Trends in biochemical sciences · 2009
    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 at 1 institution in 1 country.

Rachana TripathiCentre for Cellular and Molecular Biology, Uppal Road, Hyderabad 500007, India.
Satya Keerthi Kota
Usha K Srinivas
Centre for Cellular and Molecular Biology · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Beta-catenin is the key transducer of Wingless-type MMTV integration site family member (Wnt) signalling, upregulation of which is the cause of cancer of the colon and other tissues. In the absence of Wnt signals, beta-catenin is targeted to ubiquitin-proteasome-mediated degradation. Here we present the functional characterization of E3-ubiquitin ligase encoded by cul4B. RNAi-mediated knock-down of Cul4B in a mouse cell line C3H T10 (1/2) results in an increase in beta-catenin levels. Loss-of-function mutation in Drosophila cul4 also shows increased beta-catenin/Armadillo levels in developing embryos and displays a characteristic naked-cuticle phenotype. Immunoprecipitation experiments suggest that Cul4B and beta-catenin are part of a signal complex in Drosophila, mouse and human. These preliminary results suggest a conserved role for Cul4B in the regulation of beta-catenin levels.

Indexed as

AnimalsAnimals, Genetically ModifiedArmadillo Domain Proteinsbeta CateninCell Line, TumorCullin ProteinsDown-RegulationDrosophila melanogasterDrosophila ProteinsHumansLarvaMiceMice, Inbred C3HTranscription FactorsUbiquitin-Protein LigasesArmadillo Domain ProteinsARM protein, Drosophilabeta CateninCTNNB1 protein, mouseCul4B protein, mouseCul4 protein, DrosophilaCullin ProteinsDrosophila ProteinsTranscription FactorsUbiquitin-Protein Ligases

Identifiers

PMID17954973
OpenAlexW2090002544

What OpenQuestion holds

Textmetadata
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.