PACSIN, a brain protein that is upregulated upon differentiation into neuronal cells

Autor: Michael Leitges, Rita Lange, Gaby Vopper, Markus Plomann, Stephen W. Scheff, Mats Paulsson, Dagmar Barthels, Stanley A. Baldwin, Matthias Cramer, Harold Cremer, Uwe A.O. Heinlein
Rok vydání: 1998
Předmět:
Zdroj: European Journal of Biochemistry. 256:201-211
ISSN: 1432-1033
0014-2956
DOI: 10.1046/j.1432-1327.1998.2560201.x
Popis: To identify genes that are differentially expressed during self-repair processes in mouse brain, we screened a subtracted cDNA library enriched for brain-specific clones. One of these clones, H74, detected a 4.4-kb mRNA predominantly expressed in brain and dorsal root ganglia neurons. Expression increased continuously during the lifespan and the state of differentiation, but decreased after entorhinal-cortex lesion. A full-length cDNA clone was isolated from a cerebellum cDNA library and characterized. Se- quence analysis and database search revealed high sequence similarity to FAP52, a protein expressed in focal-adhesion contacts, and uncharacterized Echinococcus and Caenorhabditis elegans gene products. Furthermore, peptide sequences derived from human cDNA fragments showed up to 65 % sequence identity at the amino acid level. The presence of a C-terminal src homology 3 (SH3) domain and its phosphorylation by casein kinase 2 (CK2) and protein kinase C (PKC) imply a role in signaling. Here we demonstrate that the gene encodes a phosphoprotein, referred to as PACSIN, with a restricted spatial and temporal expression pattern.
Databáze: OpenAIRE