Jh. Zhang et al., Differential expression of the G protein beta(5) gene: Analysis of mouse brain, peripheral tissues, and cultured cell lines, J NEUROCHEM, 75(1), 2000, pp. 393-403
A neurally expressed heterotrimeric G protein beta subunit, G beta(5), has
been found to exhibit functional specialization with respect to its interac
tions with effector targets and G alpha subunits. A splice Variant of G bet
a(5) that contains an N-terminal 42-residue extension, G beta(5)-long, has
been described in the retina. To define better the potential range of its s
pecialized interactions, analysis of G beta(5) gene transcript and protein
expression in mouse brain and other tissues and cell lines was performed, Q
uantification by ribonuclease protection assay of G beta(5) transcript expr
ession in the developing brain demonstrates a fivefold increase that occurs
postnatally. Analysis of transcript expression by in situ hybridization an
d ribonuclease protection assay indicates that the G beta(5) gene is differ
entially expressed among multiple adult mouse brain regions, including the
motor and occipital cortex, the olfactory bulb and associated rhinencephali
c structures, hypothalamus, pontine cochlear nuclei, and Purkinje cells in
the cerebellum, G beta(5) is also expressed in several cultured cell lines
of neuroendocrine origin, including murine alpha T3-1 pituitary gonadotroph
s and GT1-7 hypothalamic cells, and rat PC12 pheochromocytoma cells. Immuno
blotting of tissue homogenates with antibodies to two peptides common to G
beta(5) and G beta(5)-long confirmed expression of G beta(5) in multiple br
ain regions and in spinal cord and expression of G beta(5)-long in retina.
Taken together, these results suggest that the specialized molecular proper
ties of G beta(5) have been adapted to diverse neural functions in the adul
t brain.