Evidence map›Paper›PMID 9926929›Full record

ArticleOncogene1999

Chimeric Wnt proteins define the amino-terminus of Wnt-1 as a transformation-specific determinant.

M A Julius, S D Rai, J Kitajewski

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 16 citations in OpenAlex.

  1. 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

3 authors at 1 institution in 1 country.

M A JuliusDepartment of Pathology and Center for Reproductive Sciences, Columbia University, College of Physicians and Surgeons, New York, New York 10032, USA.
S D Rai
J Kitajewski
Columbia University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wnt-1 induces morphological transformation of C57MG mammary epithelial cells and accumulation of cytosolic beta-catenin whereas Wnt-5a has no effect. To identify regions within the 370 amino acid Wnt-1 protein required for these functions we tested eleven chimeric genes that contained variable amounts of Wnt-1 and Wnt-5a sequence. Transformation and beta-catenin regulation in C57MG cells is controlled by amino acids that lie within 186 residues of the amino terminus of Wnt-1. Small substitutions between residues 186 and 292 reduced Wnt-1 activity. Replacement of the carboxy terminal 79 amino acids of Wnt-1 by Wnt-5a did not affect function. These results were supported by transient expression assays in 293 cells wherein beta-catenin accumulated in the cytoplasm in response to ectopic Wnt-1 expression. In 293 cells, a larger region of the amino-terminus of Wnt-1 was found to be required for beta-catenin regulation. Nonfunctional chimeras that contained at least 99 amino terminal Wnt-1 residues inhibited Wnt-1 stimulation of 293 cells. One of these chimeras inhibited both Wnt-1 and Wnt-3 activity suggesting that Wnt-1 and Wnt-3 interact with a common signaling component.

Indexed as

Cell Transformation, NeoplasticTrans-ActivatorsZebrafish ProteinsAmino Acid SequenceAnimalsbeta CateninBinding SitesCell Line, TransformedCytoskeletal ProteinsCytosolGene ExpressionHumansMiceMolecular Sequence DataProteinsProto-Oncogene Proteinsbeta CateninCTNNB1 protein, humanCTNNB1 protein, mouseCytoskeletal ProteinsProteinsProto-Oncogene ProteinsRecombinant Fusion ProteinsTrans-ActivatorsWnt1 ProteinWNT1 protein, humanWnt1 protein, mouseWnt3 ProteinWNT3 protein, humanWnt3 protein, mouseWnt-5a ProteinWNT5A protein, humanWnt ProteinsZebrafish Proteins

Identifiers

PMID9926929
OpenAlexW2334137325

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.