Rc. Bruch et al., PROTEIN-KINASE-C AND RECEPTOR KINASE GENE-EXPRESSION IN OLFACTORY RECEPTOR NEURONS, Journal of neurobiology, 33(4), 1997, pp. 387-394
Recent biochemical evidence indicates that protein kinase C (PKC) and
G-protein-coupled receptor kinases (GRKs) are involved in olfactory si
gnal termination and desensitization. The polymerase chain reaction (P
CR) was used to investigate the expression of PKC and GRK genes in olf
actory tissue and in isolated olfactory receptor neurons from channel
catfish (Ictalurus punctatus). Sequence analysis of cloned PKC PCR pro
ducts showed that the alpha, beta, delta, epsilon, and theta isotypes
were expressed in olfactory tissue, Sequence analysis of PCR products
obtained from isolated olfactory receptor neurons showed that PKC beta
and PKC delta were expressed in the receptor cells. A 600-bp GRK PCR
product was obtained from isolated olfactory neurons that shared 86% a
nd 92% amino acid sequence identity to the mammalian beta-adrenergic r
eceptor kinase gene products beta ARK1 and beta ARK2, respectively. Go
6976, a specific inhibitor of calcium-regulated PKC activity, complete
ly inhibited odorant-stimulated PKC activity in isolated olfactory cil
ia, This result suggested that odorant-stimulated PKC activity is medi
ated by the calcium-sensitive PKC beta isotype, Taken together, these
results are consistent with the conclusion that PKC beta and beta ARK
mediate odorant receptor phosphorylation and olfactory signal terminat
ion. (C) 1997 John Wiley & Sons, Inc.