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Analysis of binding and activating functions of the chick muscle acetylcholine receptorγ-subunit upstream sequence

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Summary

  1. 1.

    The skeletal muscle acetylcholine receptor comprises several subunits whose coordinated expression during myogenesis is probably controlled bycis elements in the individual subunit genes. We have previously analyzed promoter regions of theα andδ genes (Wanget al., 1988, 1990); to gain further insight into receptor regulation, we have now studied the promoter of the chick muscleγ-subunit gene.

  2. 2.

    This analysis was faciliated by the close upstream proximity of the coding region of theδ-subunit gene and the consequent brevity (740 bp) of the untranslated linker connecting the two genes (Nefet al., 1984). Nuclease protection and primer extension analysis revealed that transcription of theγ-subunit gene starts at position 56 upstream of the translational initiation site.

  3. 3.

    Nested deletions of the promoter region were employed to identify functionally important elements. A 360-bp sequence (-324 to +36) was found to activate transcription, in a position- and orientation-independent manner, during myotube formation. This sequence comprises 5 M-CAT (Nikovitset al., 1986) similarities and contains, at positions -52/-47 and -33/-28, two CANNTG (Lassaret al., 1989) motifs.

  4. 4.

    Binding experiments were performed by means of gel retardation, gel shift competition, and footprint analysis. The CANNTG motifs were found to bind MyoD and myogenin fusion proteins and to interact with proteins in nuclear extracts from cultured myotubes.

  5. 5.

    Point mutations in the CANNTG motifs revealed that these elements are crucial for full promoter activity in myotubes and essential in fibroblasts cotransfected with a myogenin expression vector.

  6. 6.

    We conclude that the activity of theγ-subunit gene is determined largely by E boxes, whichin vivo are likely to be activated by MyoD family proteins; in addition, other transactivators such as the M-CAT binding protein presumably play a role. Both CANNTG elements and M-CAT motifs are also present in theα- andδ-subunit enhancer and may therefore account for the coordinate expression of the three subunits during muscle differentiation.

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References

  • Auerbach, A., and Sachs, F. (1984). Single-channel currents from acetylcholine receptors in embryonic chick muscle. Kinetic and conductance properties of gaps within bursts.Biophys. J. 45187–198.

    Google Scholar 

  • Ausubel, F. M., Brent, R., Kingston, R. E., Moore, D. D., Seidman, J. G., Smith, J. A., and Struhl, K. (1987).Current Protocols in Molecular Biology, John Wiley and Sons, New York.

    Google Scholar 

  • Baldwin, T. J., and Burden, S. J. (1988). Isolation and characterization of the mouse acetylcholine receptor delta subunit gene: Identification of a 148-bp cis-acting region that confers myotube-specific expression.J. Cell Biol. 1072271–2279.

    Google Scholar 

  • Baldwin, T. J., and Burden, S. J. (1989). Muscle-specific gene expression controlled by a regulatory element lacking a MyoD binding site.Nature 341716–720.

    Google Scholar 

  • Bergsma, D. J., Grichnik, J. M., Gossett, L. M. A., and Schwartz, R. J. (1986). Delimitation and characterization of cis-acting DNA sequences required for the regulated expression and transcriptional control of the chicken skeletalα-actin gene.Mol. Cell. Biol. 62462–2475.

    Google Scholar 

  • Brehm, P. (1989). Resolving the structural basis for developmental changes in muscle ACh receptor function: It takes nerve.Trends Neurosci. 12174–177.

    Google Scholar 

  • Brennan, T. J., and Olson, E. N. (1990). Myogenin resides in the nucleus and acquires high affinity for a conserved enhancer element on heterodimerization.Genes Dev. 4582–595.

    Google Scholar 

  • Buonanno, A., and Merlie, J. P. (1986). Transcriptional regulation of nicotinic acetylcholine receptor genes during muscle development.J. Biol. Chem. 26111452–11455.

    Google Scholar 

  • Buskin, J. N., and Hauschka, S. D. (1989). Identification of a myocyte nuclear factor that binds to the muscle-specific enhancer of the mouse muscle creatine kinase gene.Mol. Cell. Biol. 92627–2640.

    Google Scholar 

  • Crowder, C. M., and Merlie, J. P. (1986). DNAse I-hypersenstive sites surround the mouse muscle acetylcholine receptor delta and gamma subunit gene.Proc. Natl. Acad. Sci. USA 838405–8409.

    Google Scholar 

  • Crowder, C. M., and Merlie, J. P. (1988). Stepwise activation of the mouse acetylcholine receptor delta and gamma subunit genes in clonal cell lines.Mol. Cell. Biol. 85257–5267.

    Google Scholar 

  • Davis, L. G., Dibner, M. F., and Battey, J. F. (1987).Basic Methods in Molecular Biology, Elsevier, New York.

    Google Scholar 

  • Davis, R. L., Weintraub, H., and Lassar, A. B. (1987). Expression of a single transfected cDNA converts fibroblasts to myoblasts.Cell 51987–1000.

    Google Scholar 

  • Dignam, J. D., Lebovitz, R. M., and Roeder, G. (1983). Accurate transcription by RNA polymerase II in a soluble extract from isolated mammalian nuclei.Nucl. Acids Res. 111475–1489.

    Google Scholar 

  • Duclert, A., Piette, J., and Changeux, J.-P. (1991). Influence of innervation on myogenic factors and acetylcholine receptorα-subunit mRNAs.NeuroReport 225–28.

    Google Scholar 

  • Edmondson, D. G., and Olson, E. N. (1989). A gene with homology to the myc similarity region of MyoD1 is expressed during myogenesis and is sufficient to activate the muscle differentiation program.Genes Dev. 3628–640.

    Google Scholar 

  • Eftimie, R., Brenner, H. R., and Buonanno, A. (1991). Myogenin and MyoD join a family of skeletal muscle genes regulated by electrical activity.Proc. Natl. Acad. Sci. USA 881349–1353.

    Google Scholar 

  • Galas, D., and Schmitz, A. (1978). DNase footprinting: A simple method for the detection of protein-DNA binding specificity.Nucl. Acids Res. 53157–3170.

    Google Scholar 

  • Gardner, P. D., Heinemann, S., and Patrick, J. (1987). Transcriptional regulation of nicotinic acetylcholine receptor genes: Identification of control elements of a gamma subunit gene.Mol. Brain Res. 369–76.

    Google Scholar 

  • Jia, H.-T., Tsay, H.-J., Ballivet, M., and Schmidt, J. (1989). Structural and functional analysis of the chick muscle acetylcholine receptorγ-subunit gene.Soc. Neurosci. Symp. Abstr. 151125.

    Google Scholar 

  • Klarsfeld, A., Daubas, P., Bourachot, B., and Changeux, J.-P. (1987). A 5′-flanking region of the chicken acetylcholine receptor alpha-subunit gene confers tissue specificity and developmental control of expression in transfected cells.Mol. Cell Biol. 7951–955.

    Google Scholar 

  • Lassar, A. B., Buskin, J. N., Lockshon, D., Davis, R. L., Apone, S., Hauschka, S. D., and Weintraub, H. (1989). MyoD is a sequence-specific DNA binding protein requiring a region of myc homology to bind to the muscle creatine kinase enhancer.Cell 58823–831.

    Google Scholar 

  • Mar, J. H., and Ordahl, C. P. (1990). M-CAT binding factor, a novel trans-acting factor governing muscle-specific transcription.Mol. Cell. Biol. 104271–4283.

    Google Scholar 

  • Maxam, A., and Gilbert, W. (1980). Sequencing end-labeled DNA with base-specific chemical cleavages.Meth. Enzymol. 65499–560.

    Google Scholar 

  • Miller, J. H. (1972).Experiments in Molecular Genetics, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York.

    Google Scholar 

  • Miner, J. H., and Wold, B. (1990). Herculin, a fourth member of the MyoD family of myogenic regulatory genes.Proc. Natl. Acad. Sci. USA 871089–1093.

    Google Scholar 

  • Moss, S. J., Beeson, D. M. W., Jackson, J. F., Darlison, M. G., and Barnard, E. A. (1987). Differential expression of nicotinic acetylcholine receptor genes in innervated and denervated chicken muscle.EMBO J. 63917–3921.

    Google Scholar 

  • Nef, P., Mauron, A., Stalder, A., Alliod, C., and Ballivet, M. (1984). Structure, linkage and sequence of the two genes encoding the delta and gamma subunits of the nicotinic acetylcholine receptor.Proc. Natl. Acad. Sci. USA 817975–7979.

    Google Scholar 

  • Piette, J., Klarsfeld, A., and Changeux, J.-P. (1989). Interaction of nuclear factors with the upstream region of the alpha-subunit gene of chick muscle acetylcholine receptor: Variations with muscle differentiation and denervation.EMBO J. 8687–694.

    Google Scholar 

  • Piette, J., Bessereau, J.-L., Huchet, M., and Changeux, J.-P. (1990). Two adjacent MyoD1-binding sites regulate expression of the acetylcholine receptor alpha-subunit gene.Nature 345353–355.

    Google Scholar 

  • Ricksten, A., Olsson, A., Andersson, T., and Rymo, L. (1988). The 5′ flanking region of the gene for the Epstein-Barr virus-encoded nuclear antigen 2 contains a cell type specific cis-acting regulatory element that activates transcription in transfected B-cells.Nucl. Acids Res. 168391–8411.

    Google Scholar 

  • Ross, A. F., Rapuano, M., Schmidt, J., and Prives, J. M. (1987). Phosphorylation and assembly of nicotinic acetylcholine receptor subunits in cultured chick muscle cells.J. Biol. Chem. 26214640–14647.

    Google Scholar 

  • Schimmel, S. D., Kent, C., and Vagelos, P. R. (1977). Isolation of plasma membranes from cultured muscle cells.Methods Cell Biol. 25289–301.

    Google Scholar 

  • Schuetze, S. M. (1980). The acetylcholine channel open time in chick muscle is not decreased following innervation.J. Physiol. (London)303111–124.

    Google Scholar 

  • Shibahara, S., Kubo, T. Perski, H. J., Takahashi, H., Noda, M., and Numa, S. (1985). Cloning and sequence analysis of human genomic DNA encoding gamma subunit precursor of muscle acetylcholine receptor.Eur J. Biochem. 14615–22.

    Google Scholar 

  • Tsay, H.-J., and Schmidt, J. (1989). Skeletal muscle denervation activates acetylcholine receptor genes.J. Cell Biol. 1081523–1526.

    Google Scholar 

  • Wang, X.-M., Tsay, H.-J., and Schmidt, J. (1990). 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.EMBO J. 9783–790.

    Google Scholar 

  • Wang, Y., Xu, H.-P., Wang, X.-M., and Schmidt, J. (1988). A cell type-specific enhancer drives expression of the chick muscle acetylcholine receptor alpha-subunit gene.Neuron 1527–534.

    Google Scholar 

  • Weintraub, H., Davis, R., Lockshon, D., and Lassar, A. (1990). MyoD binds cooperatively to two sites in a target enhancer sequence: Occupancy of two sites is required for activation.Proc. Natl. Acad. Sci. USA 875623–5627.

    Google Scholar 

  • Weintraub, H., Davis, R., Tapscott, S., Thayer, M., Krause, M., Benezra, R., Blackwell, T. K., Turner, D., Rupp, R., Hollenberg, S., Zhuang, Y., and Lassar, A. (1991). The MyoD gene family: Nodal point during specification of the muscle cell lineage.Science 251 761–766.

    Google Scholar 

  • Wentworth, B. M., Donoghue, M., Engert, J. C., Berglund, E. B., and Rosenthal, N. (1991). Paired MyoD-binding sites regulate myosin light chain gene expression.Proc. Natl. Acad. Sci. USA 881242–1246.

    Google Scholar 

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Jia, HT., Tsay, HJ. & Schmidt, J. Analysis of binding and activating functions of the chick muscle acetylcholine receptorγ-subunit upstream sequence. Cell Mol Neurobiol 12, 241–258 (1992). https://doi.org/10.1007/BF00712929

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  • DOI: https://doi.org/10.1007/BF00712929

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