Note. The dog clone c5fw cDNA sequence has been deposited in the DDBJ, EMBL and Genbank databases under the accession number >emb|X99144|e996426. The human clone c5fw and clone c8fi cDNA sequences hove been deposited under the accession numbers [D87119] and [AJ0004HO], respectively.
Characterization of a Phosphoprotein whose mRNA is Regulated by the Mitogenic Pathways in Dog Thyroid Cells
Article first published online: 16 JUL 2004
European Journal of Biochemistry
Volume 248, Issue 3, pages 660–668, September 1997
How to Cite
Wilkin, F., Suarez-Huerta, N., Robaye, B., Peetermans, J., Libert, F., Dumont, J. E. and Maenhaut, C. (1997), Characterization of a Phosphoprotein whose mRNA is Regulated by the Mitogenic Pathways in Dog Thyroid Cells. European Journal of Biochemistry, 248: 660–668. doi: 10.1111/j.1432-1033.1997.t01-1-00660.x
- Issue published online: 16 JUL 2004
- Article first published online: 16 JUL 2004
- (Received 21 April/7 July 1997) – EJB 97 0566/1
We have isolated cDNA clones encoding the dog and human forms of a novel protein whose function is still unknown. Sequence analysis indicates that dog clone c5fw protein contains 343 amino acid residues, several potential phosphorylation sites, and two of the 12 conserved subdomains (VIII and IX) that fold into a common catalytic core structure of the large family of protein kinases. Human clone c5fw shares 95% amino acid identity with its dog counterpart. We have also isolated another human-related clone c5fw sharing 70% amino acid identity with the dog sequence. We transiently expressed c-myc epitope-tagged clone c5fw protein in COS-7 cells and infected thyrocytes in primary culture with a recombinant adenovirus containing clone c5fw cDNA (adenovirus c5fw).In both experiments, a 46-kDa protein was detected and subsequently more extensively characterized. By two-dimensional gel electrophoresis and V8 protease digestion, we showed that this overexpressed protein is phosphorylated on different sites. Moreover, cells stimulated with thyrotropin or epiderinal growth factor, thyrotropin and fetal calf serum increased the level of clone c5fw protein produced after infection by adenovirus containing clone c5fw. The disappearance of this 46-kDa protein after 1 h of puromycin treatment indicates that it is a labile protein. Immunofluorescence and subcellular fractionation analysis have revealed that c-myc-tagged clone c5fw was insoluble and localized mainly in the cytoplasm, in the form of granules.