Cloning and characterization of a novel serine/threonine protein kinase gene expressed predominantly in developing brain

Citation
K. Nara et al., Cloning and characterization of a novel serine/threonine protein kinase gene expressed predominantly in developing brain, EUR J BIOCH, 268(9), 2001, pp. 2642-2651
Citations number
38
Categorie Soggetti
Biochemistry & Biophysics
Journal title
EUROPEAN JOURNAL OF BIOCHEMISTRY
ISSN journal
00142956 → ACNP
Volume
268
Issue
9
Year of publication
2001
Pages
2642 - 2651
Database
ISI
SICI code
0014-2956(200105)268:9<2642:CACOAN>2.0.ZU;2-V
Abstract
We have isolated a rat gene, sbk, that encodes a novel serine/threonine pro tein kinase possessing a consensus sequence for an SH3-binding domain from developing rat brain. Rat SBK comprises 417 amino-acid residues consisting of a serine/threonine protein kinase consensus sequence followed by a C-ter minal proline-rich region. Sequence comparison with other known kinases rev ealed that sbk belongs to a novel family of serine/threonine protein kinase s structurally related to a Xenopus gastrula-specific protein kinase, Pk9.7 . An in vitro kinase assay demonstrated that the SBK protein autophosphoryl ates at serine/threonine residues. Transcripts of sbk were strongly detecte d in brain, and the distribution shows an association with neurons but not glial cells. A marked increase in sbk transcripts was observed in developin g brain in the late embryonic stage when dramatic neuronal proliferation, m igration, and maturation occur. Fluorescence in situ hybridization analysis was used to map sbk to mouse chromosome 7F1-F3 and rat chromosome 1q21. Th ese data suggest a role for SBK in signal-transduction pathways related to the control of brain development.