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Research Article

A novel myoblast enhancer element mediates MyoD transcription.

S J Tapscott, A B Lassar, H Weintraub
S J Tapscott
Fred Hutchinson Cancer Research Center, Howard Hughes Medical Institute Laboratory, Seattle, Washington 98104.
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A B Lassar
Fred Hutchinson Cancer Research Center, Howard Hughes Medical Institute Laboratory, Seattle, Washington 98104.
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H Weintraub
Fred Hutchinson Cancer Research Center, Howard Hughes Medical Institute Laboratory, Seattle, Washington 98104.
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DOI: 10.1128/MCB.12.11.4994
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ABSTRACT

The MyoD gene can orchestrate the expression of the skeletal muscle differentiation program. We have identified the regions of the gene necessary to reproduce transcription specific to skeletal myoblasts and myotubes. A proximal regulatory region (PRR) contains a conserved TATA box, a CCAAT box, and a GC-rich region that includes a consensus SP1 binding site. The PRR is sufficient for high levels of skeletal muscle-specific activity in avian muscle cells. In murine cells the PRR alone has only low levels of activity and requires an additional distal regulatory region to achieve high levels of muscle-specific activity. The distal regulatory region differs from a conventional enhancer in that chromosomal integration appears necessary for productive interactions with the PRR. While the Moloney leukemia virus long terminal repeat can enhance transcription from the MyoD PRR in both transient and stable assays, the simian virus 40 enhancer cannot, suggesting that specific enhancer-promoter interactions are necessary for PRR function.

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A novel myoblast enhancer element mediates MyoD transcription.
S J Tapscott, A B Lassar, H Weintraub
Molecular and Cellular Biology Nov 1992, 12 (11) 4994-5003; DOI: 10.1128/MCB.12.11.4994

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A novel myoblast enhancer element mediates MyoD transcription.
S J Tapscott, A B Lassar, H Weintraub
Molecular and Cellular Biology Nov 1992, 12 (11) 4994-5003; DOI: 10.1128/MCB.12.11.4994
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