Evidence map›Paper›PMID 25143387›Full record

ArticleThe Journal of biological chemistry2014

Fbxo45 inhibits calcium-sensitive proteolysis of N-cadherin and promotes neuronal differentiation.

Fu-Zon Chung, Anagh A Sahasrabuddhe, Kaiyu Ma, Xiaofei Chen, Venkatesha Basrur, Megan S Lim, Kojo S J Elenitoba-Johnson

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. GLUL stabilizes N-Cadherin by antagonizingActa pharmaceutica Sinica. B · 2024
    Article
  4. Article
  5. Inhibitors Targeting the F-BOX Proteins.Cell biochemistry and biophysics · 2023
    Review
  6. Article
  7. Article
  8. Article
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  10. Article
  11. Article
  12. Article
  13. Review
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  15. Article
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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

7 authors at 1 institution in 1 country.

Fu-Zon ChungFrom the Department of Pathology.
Anagh A SahasrabuddheFrom the Department of Pathology.
Kaiyu MaFrom the Department of Pathology.
Xiaofei ChenFrom the Department of Pathology.
Venkatesha BasrurFrom the Department of Pathology.
Megan S LimFrom the Department of Pathology, the Center for Computational Medicine and Bioinformatics, and.
Kojo S J Elenitoba-JohnsonFrom the Department of Pathology, the Center for Computational Medicine and Bioinformatics, and the Protein Folding Diseases Initiative, University of Michigan Medical School, Ann Arbor, Michigan 48109 kojoelen@umich.edu.
University of Michigan–Ann Arbor · US

Funding

Proteomic analysis of api2-MALT1 positive gastric MALT lymphomaR01CA136905 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELENITOBA-JOHNSON, KOJO S. J. · 2009 to 2013
$1.4M
Proteomic biomarkers of ALK+ lymphomaR01CA140806 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LIM, MEGAN S. · 2010 to 2013
$1.2M
NCI NIH HHS R01 CA136905NCI NIH HHS R01 CA140806NIDCR NIH HHS R01 DE119249
6 · The paper itself

Abstract

Fbxo45 is an atypical E3 ubiquitin ligase, which specifically targets proteins for ubiquitin-mediated degradation. Fbxo45 ablation results in defective neuronal differentiation and abnormal formation of neural connections; however, the mechanisms underlying these defects are poorly understood. Using an unbiased mass spectrometry-based proteomic screen, we show here that N-cadherin is a novel interactor of Fbxo45. N-cadherin specifically interacts with Fbxo45 through two consensus motifs overlapping the site of calcium-binding and dimerization of the cadherin molecule. N-cadherin interaction with Fbxo45 is significantly abrogated by calcium treatment. Surprisingly, Fbxo45 depletion by RNAi-mediated silencing results in enhanced proteolysis of N-cadherin. Conversely, ectopic expression of Fbxo45 results in decreased proteolysis of N-cadherin. Fbxo45 depletion results in dramatic reduction in N-cadherin expression, impaired neuronal differentiation, and diminished formation of neuronal processes. Our studies reveal an unanticipated role for an F-box protein that inhibits proteolysis in the regulation of a critical biological process.

Indexed as

Amino Acid SequenceAnimalsBinding SitesCadherinsCalciumCell DifferentiationCell LineEmbryo, MammalianEmbryonic Stem CellsF-Box ProteinsGene Expression Regulation, DevelopmentalHumansMiceMolecular Sequence DataNeuronsProtein BindingCadherinsCalciumCdh2 protein, mouseF-Box ProteinsFbxo45 protein, mouseRNA, Small InterferingCalciumCell DifferentiationEndocytosisIntramembrane ProteolysisPlasma Membrane

Identifiers

PMID25143387
PMCPMC4192496
OpenAlexW1994186085

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.