Evidence map›Paper›PMID 1672045›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1991

Native avian c-erbB gene expresses a secreted protein product corresponding to the ligand-binding domain of the receptor.

N J Maihle, T W Flickinger, M A Raines, M L Sanders, H J Kung

Open access · greenAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1991. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

6 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Identification and molecular cloning of a soluble human granulocyte-macrophage colony-stimulating factor receptor.Proceedings of the National Academy of Sciences of the United States of America · 1991
    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

5 authors at 2 institutions in 1 country.

N J MaihleDepartment of Biochemistry and Molecular Biology, Mayo Clinic and Foundation, Rochester, MN 55905.
T W Flickinger
M A Raines
M L Sanders
H J Kung
Mayo Clinic · USCase Western Reserve University · US

Funding

ERBB KINASE ACTIVATION AND TRANSFORMATIONR01CA039207 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI KUNG, HSING-JIEN · 1986 to 2004
$1.5M
TISSUE-SPECIFIC ONCOGENESIS MEDIATED BY C-ERB-BR01CA051197 · NCI · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI MAIHLE, NITA J. · 1990 to 1994
–
ERBB KINASE ACTIVATION AND TRANSFORMATIONR37CA039207 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI KUNG, HSING-JIEN · 1991 to 1999
–
NCI NIH HHS CA 39207NCI NIH HHS CA 51197
6 · The paper itself

Abstract

A primer-directed cDNA library was used to obtain cDNA clones corresponding to the 5' end (i.e., the ligand-binding domain) of the avian c-erbB gene. Bacterial c-erbB fusion proteins were synthesized and used to obtain polyclonal antisera specific for the ligand-binding domain of the avian receptor. These antisera and antisera specific for the carboxyl terminal domain of the chicken c-erbB gene product have been used to study the native protein products of the c-erbB locus in primary cell cultures by in vivo labeling and immunoprecipitation. Our studies reveal that three c-erbB gene products of Mr 300,000, Mr 170,000, and Mr 95,000 are synthesized in uninfected chicken embryo fibroblasts. Only the Mr 300,000 and Mr 170,000 species can be precipitated by using antisera specific for the cytoplasmic domain of the c-erbB product. The 95,000 species is not recognized by the antiserum directed against the carboxyl-terminal domain of c-erbB and is specifically released into the culture medium. Northern transfer studies reveal a lower molecular weight transcript of approximately 2.6 kilobases that selectively hybridizes to the ligand-binding domain of the avian c-erbB gene product but does not hybridize with probes specific for the cytoplasmic kinase domain of c-erbB. An additional cDNA clone corresponding to this transcript has been isolated, and its sequence suggests it may arise via alternative processing. Together, these data suggest that a truncated form of this growth factor receptor--i.e., a Mr 95,000 species--is synthesized from a low molecular weight c-erbB transcript that exclusively encodes the ligand-binding domain of the receptor. Secretion of truncated growth factor receptors has been reported recently in several systems, and our results are discussed in the light of these findings.

Indexed as

Proto-OncogenesAmino Acid SequenceAnimalsBase SequenceBinding SitesBlotting, NorthernCells, CulturedChick EmbryoDNA ProbesErb-b2 Receptor Tyrosine KinasesFibroblastsGene LibraryHumansLigandsMolecular Sequence DataOligonucleotide ProbesDNA ProbesErb-b2 Receptor Tyrosine KinasesLigandsOligonucleotide ProbesProtein-Tyrosine KinasesProto-Oncogene Proteins

Identifiers

PMID1672045
PMCPMC51118
OpenAlexW1981928345

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.