DIK, a novel protein kinase that interacts with protein kinase Cdelta. Cloning, characterization, and gene analysis.
A novel serine/threonine kinase, termed DIK, was cloned using the yeast two-hybrid system to screen a cDNA library from the human keratinocyte cell line HaCaT with the catalytic domain of rat protein kinase Cdelta (PKCdelta(cat)) cDNA as bait. The predicted 784-amino acid polypeptide with a calculated molecular mass of 86 kDa contains a catalytic kinase domain and a putative regulatory domain with ankyrin-like repeats and a nuclear localization signal. Expression of DIK at the mRNA and protein level could be demonstrated in several cell lines. The dik gene is located on chromosome 21q22.3 and possesses 8 exons and 7 introns. DIK was synthesized in an in vitro transcription/translation system and expressed as recombinant protein in bacteria, HEK, COS-7, and baculovirus-infected insect cells. In the in vitro system and in cells, but not in bacteria, various post-translationally modified forms of DIK were produced. DIK was shown to exhibit protein kinase activity toward autophosphorylation and substrate phosphorylation. The interaction of PKCdelta(cat) and PKCdelta with DIK was confirmed by coimmunoprecipitation of the proteins from HEK cells transiently transfected with PKCdelta(cat) or PKCdelta and DIK expression constructs.
Pubmed ID: 10948194 RIS Download
Amino Acid Sequence | Animals | Base Sequence | Blotting, Western | Catalytic Domain | Cell Line | Chromosome Mapping | Chromosomes, Human, Pair 21 | Exons | Gene Expression Profiling | Humans | Introns | Isoenzymes | Keratinocytes | Molecular Sequence Data | Phosphorylation | Precipitin Tests | Protein Kinase C | Protein Kinase C-delta | Protein Structure, Tertiary | Protein-Serine-Threonine Kinases | RNA, Messenger | Rats | Recombinant Fusion Proteins | Staurosporine | Transfection | Two-Hybrid System Techniques