Linked Life Data

11847211

Source:http://linkedlifedata.com/resource/pubmed/id/11847211

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
17
pubmed:dateCreated
2002-4-22
pubmed:abstractText
The receptor for the macrophage colony-stimulating factor (CSF-1, also termed M-CSF), the tyrosine kinase c-Fms, was originally determined to be the oncogene product of the McDonough strain of feline sarcoma virus, v-Fms. The structural difference between c-Fms and v-Fms amounts to only five point mutations in the extracellular domain, two mutations in the cytoplasmic domain, and the replacement of 50 amino acids by 14 unrelated amino acids at the C-terminal tail. Here, we have identified c-Cbl as the direct binding partner for c-Fms. c-Cbl binds to phosphotyrosine residue 977 at the C-terminal end of feline c-Fms, which is absent in v-Fms. The replacement of the C-terminal end of v-Fms by the corresponding part of c-Fms (vc-Fms) restored the binding potential. As a result, vc-Fms reduced the transforming potency of v-Fms. The overexpression of Cbl did not influence the v-Fms-transformed phenotype, although c-Cbl forms a complex with v-Fms indirectly. In contrast, the expression of Cbl drastically reduced the vc-Fms-transformed phenotype and the activation of Erk and enhanced Fms ubiquitination via phosphotyrosine residue 977. Furthermore, the replacement of tyrosine 977 into phenylalanine in feline c-Fms and vc-Fms reduced the Cbl-dependent ubiquitination. These data suggest that an indirect association of c-Cbl via multimeric complex induced a different signaling pathway from the pathway induced by c-Cbl direct interaction.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
26
pubmed:volume
277
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
14635-40
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:11847211-3T3 Cells, pubmed-meshheading:11847211-Animals, pubmed-meshheading:11847211-Cell Transformation, Neoplastic, pubmed-meshheading:11847211-Down-Regulation, pubmed-meshheading:11847211-Humans, pubmed-meshheading:11847211-Macrophage Colony-Stimulating Factor, pubmed-meshheading:11847211-Mice, pubmed-meshheading:11847211-Oncogene Protein gp140(v-fms), pubmed-meshheading:11847211-Phenotype, pubmed-meshheading:11847211-Point Mutation, pubmed-meshheading:11847211-Protein Binding, pubmed-meshheading:11847211-Proto-Oncogene Proteins, pubmed-meshheading:11847211-Proto-Oncogene Proteins c-cbl, pubmed-meshheading:11847211-Receptor, Macrophage Colony-Stimulating Factor, pubmed-meshheading:11847211-Tyrosine, pubmed-meshheading:11847211-Ubiquitin, pubmed-meshheading:11847211-Ubiquitin-Protein Ligases
pubmed:year
2002
pubmed:articleTitle
c-Cbl associates directly with the C-terminal tail of the receptor for the macrophage colony-stimulating factor, c-Fms, and down-modulates this receptor but not the viral oncogene v-Fms.
pubmed:affiliation
Institut für Biochemie, OE 4310, Medizinische Hochschule Hannover, Carl-Neuberg-Str. 1, D-30623 Hannover, Germany.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't