MOLECULAR-CLONING OF A MOUSE G-PROTEIN-ACTIVATED K-RNAS IN MOUSE-BRAIN( CHANNEL (MGIRK1) AND DISTINCT DISTRIBUTIONS OF 3 GIRK (GIRK1, GIRK2AND GIRK3) MESSENGER)
T. Kobayashi et al., MOLECULAR-CLONING OF A MOUSE G-PROTEIN-ACTIVATED K-RNAS IN MOUSE-BRAIN( CHANNEL (MGIRK1) AND DISTINCT DISTRIBUTIONS OF 3 GIRK (GIRK1, GIRK2AND GIRK3) MESSENGER), Biochemical and biophysical research communications, 208(3), 1995, pp. 1166-1173
We cloned the mouse brain G-protein-activated K+ channel 1 (mGIRK1) cD
NA and determined the complete nucleotide and amino acid sequences of
the coding region. In in situ hybridization using specific oligonucleo
tide probes, the signals for the three mGIRK (mGIRK1, mGIRK2 and mGIRK
3) mRNAs were shown to be distributed widely as well as differently in
most brain regions except for the caudate-putamen. Further, at]east o
ne, usually several, mGIRK mRNA with variable combinations was observe
d in most brain regions. These findings suggested that mGIRK channels
may be essential in most brain regions in a signal transduction mediat
ed by various G-protein-coupled receptors and that different subunit o
rganizations of the mGIRK channel might occur in different neurons, re
sulting in diversity of their channel function in vivo. (C) 1995 Acade
mic Press, Inc.