Members of the cAMP-dependent second-messenger pathway have been described
as regulators of cellular growth and differentiation and were consequently
implicated in a variety of embryogenic processes including brain developmen
t. Moreover, recent data suggest an indispensable role for cAMP-dependent p
rotein kinases (PKAs) in neuronal differentiation and synaptic plasticity.
Using a degenerate primer-based approach, we have identified a novel murine
gene closely related to the human cAMP-dependent protein kinase PRIM on Xp
22.3. This gene (Pkare) was mapped to the region near the centromere of the
murine X chromosome and is expressed in a variety of adult organs includin
g kidney, liver, spleen, testis, ovary, lung, heart, and brain. Antisense i
n situ hybridization on staged mouse embryos revealed a highly distinctive
expression pattern during neuronal development, with elevated Pkare express
ion observed only in differentiating neurons within the first ganglion, the
dorsal root ganglia, and the mantle layer of the telencephalon, Based on t
he close relationship with the catalytic PKA subunits and its distinct expr
ession in differentiating neuronal cells, Pkare might represent a novel com
ponent of the cAMP-regulated pathways involved in brain development and fun
ction, (C) 2000 Academic Press.