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Expression of the acetylcholine receptor delta‐subunit gene in differentiating chick muscle cells is activated by an element that contains two 16 bp copies of a segment of the alpha‐subunit enhancer.
Author(s) -
Wang X.M.,
Tsay H.J.,
Schmidt J.
Publication year - 1990
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1002/j.1460-2075.1990.tb08174.x
Subject(s) - biology , interleukin 10 receptor, alpha subunit , protein subunit , enhancer , g alpha subunit , acetylcholine receptor , interleukin 5 receptor alpha subunit , gamma aminobutyric acid receptor subunit alpha 1 , alpha (finance) , gene expression , gene , microbiology and biotechnology , receptor , genetics , medicine , construct validity , nursing , patient satisfaction
The acetylcholine receptor is a multimeric membrane protein whose expression is activated during muscle differentiation and upon denervation of adult muscle. To gain insight into the coordinate expression of receptor subunits during myogenesis we have analyzed the chick muscle receptor delta‐subunit gene upstream region. The delta‐subunit gene lacks canonical promoter elements (CCAAT and TATA boxes). Nuclease protection and primer extension analysis revealed that transcription starts at six major and several minor sites between ‐110 and ‐30 upstream of the translational initiation site; two sites, at positions ‐77 and ‐66, give rise to approximately 50% of all transcripts. Using nested deletions of the proximal 960 bp of the 5′ flanking region of this gene we have identified a 62 bp sequence (‐207 to ‐146) that activates transcription in a position independent manner. This enhancer‐like element is activated during myotube formation; it contains two distinct functional moieties, each resembling the same 16 bp portion of the stage and tissue specific alpha‐subunit gene enhancer which we have characterized previously [Wang et al. (1988) Neuron, 1, 527‐534]. This common element, which also comprises several previously proposed skeletal muscle specific motifs [Buskin, J. N. and Hauschka, S. D. (1989) Mol. Cell Biol., 9, 2627‐2640; Mar, J. H. and Ordahl, C. P. (1988) Proc. Natl. Acad. Sci. USA, 85, 6404‐6408], may account for the coordinate expression of the two subunits. The cell specificity of the delta‐subunit gene 5′ flanking region is partly due to the enhancer, partly to an inhibitory element upstream of ‐207.