1. Academic Validation
  2. Molecular cloning and expression of a new putative inositol 1,4,5-trisphosphate 3-kinase isoenzyme

Molecular cloning and expression of a new putative inositol 1,4,5-trisphosphate 3-kinase isoenzyme

  • Biochem J. 1991 Sep 15;278 ( Pt 3)(Pt 3):883-6. doi: 10.1042/bj2780883.
K Takazawa 1 J Perret J E Dumont C Erneux
Affiliations

Affiliation

  • 1 Institut de Recherche Interdisciplinaire (IRIBHN), Université Libre de Bruxelles, Belgium.
Abstract

A human hippocampus cDNA library in lambda ZAP II was screened by hybridization with a rat brain inositol 1,4,5-trisphosphate (InsP3) 3-kinase cDNA. Two clones (hh6 and hh3) were isolated and sequenced. The insert of clone hh6 was shown to correspond to the 3' end of the coding sequence of 50,000-Mr InsP3 3-kinase (referred to as 3-kinase-A). Sequencing of the clone hh3 insert yielded an open reading frame encoding a 472-amino acid protein with a calculated Mr of 53,451 (referred to as 3-kinase-B). The C-terminal part of 3-kinase-B (residues 187-462) was 68% identical with 3-kinase-A in amino acid sequence. The cDNA of clone hh3 was rescued as a Bluescript plasmid and expressed in Escherichia coli as a beta-galactosidase fusion product. It showed InsP3 3-kinase activity that was stimulated in the presence of Ca2+/Calmodulin (more than 7-fold in a crude Bacterial lysate from expressed plasmid). Regeneration of InsP3 3-kinase activity after SDS/PAGE identified a major polypeptide (Mr 60,000-65,000). The Km for InsP3 of expressed 3-kinase-B was 1.6 microM. These data provide molecular evidence for the existence of InsP3 3-kinase isoenzymes.

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