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J Biol Chem, Vol. 273, Issue 24, 15131-15137, June 12, 1998

Functional Properties of the Neuronal Nicotinic Acetylcholine Receptor beta 3 Promoter in the Developing Central Nervous System

Tomas Roztocil, Lidia Matter-Sadzinski, Marie Gomez, Marc Ballivet, and Jean-Marc Matter

From the Department of Biochemistry, Sciences II, University of Geneva, 1211 Geneva 4, Switzerland

Within the chick central nervous system, expression of the beta 3 nicotinic acetylcholine receptor gene is restricted to a subset of retinal neurons, the majority of which are ganglion cells. Transient transfection in retinal neurons and in neural and non-neural cells from other regions of the chick embryo allowed the identification of the cis-regulatory domain of the beta 3 gene. Within this domain, a 75-base pair fragment located immediately upstream of the transcription start site suffices to reproduce the neuron-specific expression pattern of beta 3. This fragment encompasses an E-box and a CAAT box, both of which are shown to be key positive regulatory elements of the beta 3 promoter. Co-transfection experiments into retinal, telencephalic, and tectal neurons with plasmid reporters of beta 3 promoter activity and a number of vectors expressing different neuronal (ASH-1, NeuroM, NeuroD, CTF-4) and non-neuronal (MyoD) basic helix-loop-helix transcription factors indicate that the cis-regulatory domain of beta 3 has the remarkable property of discriminating accurately between related members of the basic helix-loop-helix protein family. The sequence located immediately 3' of the E-box participates in this selection, and the E-box acts in concert with the nearby CAAT box.


Copyright © 1998 by The American Society for Biochemistry and Molecular Biology, Inc.
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