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J Biol Chem, Vol. 273, Issue 24, 15131-15137, June 12, 1998
Functional Properties of the Neuronal Nicotinic Acetylcholine
Receptor 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 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 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 3. This fragment encompasses an E-box and a
CAAT box, both of which are shown to be key positive regulatory
elements of the 3 promoter. Co-transfection experiments into
retinal, telencephalic, and tectal neurons with plasmid reporters of
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 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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Copyright © 1998 by the American Society for Biochemistry and Molecular Biology.
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