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Bacterial artificial chromosome transgenic analysis of dynamic expression patterns of regulator of G-protein signaling 4 during development. I. Cerebral cortex.
- Ebert PJ, Campbell DB, Levitt P
Neuroscience. 2006 Nov 3;142(4):1145-61. Epub 2006 Sep 25.
Signaling through G-protein-coupled receptors is modulated by a family of regulator of G protein
signaling (RGS) proteins
that have been implicated in several neurological
and psychiatric
disorders. Defining the detailed expression patterns and developmental regulation
of RGS proteins
has been hampered by an absence of antibodies
useful for mapping.
We have utilized bacterial
artificial chromosome
(BAC) methods to create transgenic mice
that express GFP under the control
of endogenous regulator of G-protein signaling 4 (RGS4) enhancer elements. This report focuses on expression patterns in the developing and mature cerebral cortex.
Based on reporter distribution, RGS4 is expressed by birth in neurons
across all
cortical
domains, but in different patterns that suggest region- and layer-specific regulation.
Peak expression typically occurs before puberty,
with complex down-regulation by adulthood. Deep and superficial neurons,
in particular, vary in their patterns across developmental age and region and, in primary sensory
cortices, layer IV neurons
exhibit low or no expression of the GFP reporter. These data suggest that altering RGS4 function will produce a complex neuronal
phenotype
with cell- and subdomain-specificity in the cerebral cortex.
This abstract at PubMed.