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Mol. Cell. Biol., 01 1998, 69-77, Vol 18, No. 1
BL Black, JD Molkentin and EN Olson
Establishment of skeletal muscle lineages is controlled by the MyoD family
of basic helix-loop-helix (bHLH) transcription factors. The ability of
these factors to initiate myogenesis is dependent on two conserved amino
acid residues, alanine and threonine, in the basic domains of these
factors. It has been postulated that these two residues may be responsible
for the initiation of myogenesis via interaction with an essential myogenic
cofactor. The myogenic bHLH proteins cooperatively activate transcription
and myogenesis through protein-protein interactions with members of the
myocyte enhancer factor 2 (MEF2) family of MADS domain transcription
factors. MyoD-E12 heterodimers interact with MEF2 proteins to
synergistically activate myogenesis, while homodimers of E12, which lack
the conserved alanine and threonine residues in the basic domain, do not
interact with MEF2. We have examined whether the myogenic alanine and
threonine in the MyoD basic region are required for interaction with MEF2.
Here, we show that substitution of the MyoD basic domain with that of E12
does not prevent interaction with MEF2. Instead, the inability of
alanine-threonine mutants of MyoD to initiate myogenesis is due to a
failure to transmit transcriptional activation signals provided either from
the MyoD or the MEF2 activation domain. This defect in transcriptional
transmission can be overcome by substitution of the MyoD or the MEF2
activation domain with the VP16 activation domain. These results
demonstrate that myogenic bHLH-MEF2 interaction can be uncoupled from
transcriptional activation and support the idea that the myogenic residues
in myogenic bHLH proteins are essential for transmission of a
transcriptional activation signal.
Copyright © 1998, American Society for Microbiology
Multiple roles for the MyoD basic region in transmission of transcriptional activation signals and interaction with MEF2
Department of Molecular Biology and Oncology, The University of Texas Southwestern Medical Center, Dallas 75235-9148, USA.
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