PT  - JOURNAL ARTICLE
AU  - Jennifer McDonough
AU  - Evan Deneris
TI  - β43′: An Enhancer Displaying Neural-Restricted Activity Is Located in the 3′-Untranslated Exon of the Rat Nicotinic Acetylcholine Receptor β4 Gene
AID  - 10.1523/JNEUROSCI.17-07-02273.1997
DP  - 1997 Apr 01
TA  - The Journal of Neuroscience
PG  - 2273--2283
VI  - 17
IP  - 7
4099  - http://www.jneurosci.org/content/17/7/2273.short
4100  - http://www.jneurosci.org/content/17/7/2273.full
SO  - J. Neurosci.1997 Apr 01; 17
AB  - Members of a neuronal nicotinic acetylcholine receptor subunit gene cluster ordered β4, α3, α5 in the vertebrate genome are expressed in highly restricted patterns in the PNS and CNS. Nothing is known, however, about the regulatory elements that control transcription of these genes in selected neuronal cell populations. We report here a novel enhancer, designated β43′, that is positioned in the β4 3′-untranslated exon. It is composed of two nearly identical 37 bp direct repeats that are separated by 6 bp. Multimerization of the enhancer upstream of the α3 minimal promoter results in synergistic activation. Analysis in different cell types, including three neural lines and primary keratinocytes, shows that β43′ is preferentially active in the neural line PC12, which expresses all members of the cluster. Mobility shift assays reveal a cell-type-specific complex, which forms with the first repeat of the enhancer and PC12 extracts. Complexes co-migrating with the PC12 cell complex are not detected with extracts from other lines, which suggests that PC12 cells contain a differentially expressed factor that may be important for the restricted activity of β43′. The cell-type-specific activity of the β43′ enhancer suggests that it is important for regulating restricted expression patterns of one or more clustered neuronal acetylcholine receptor genes. Its location within the β4 gene may be a selective pressure for maintaining tight linkage of clustered neuronal nAchR genes.