Molkentin J D, Black B L, Martin J F, Olson E N
Department of Biochemistry and Molecular Biology University of Texas M. D. Anderson Cancer Center, Houston 77030, USA.
Cell. 1995 Dec 29;83(7):1125-36. doi: 10.1016/0092-8674(95)90139-6.
Members of the myocyte enhancer factor-2 (MEF2) family of MADS domain transcription factors cannot induce myogenesis in transfected fibroblasts, but when coexpressed with the myogenic basic-helix-loop-helix (bHLH) proteins MyoD or myogenin they dramatically increase the extent of myogenic conversion above that seen with either myogenic bHLH factor alone. This cooperativity required direct interactions between the DNA-binding domains of MEF2 and the myogenic bHLH factors, but only one of the factors needed a transactivation domain, and only one of the factors needed to be bound to DNA. These interactions allow either factor to activate transcription through the other's binding site and reveal a novel mechanism for indirect activation of gene expression via protein-protein interactions between the DNA-binding domains of heterologous classes of transcription factors.
MADS结构域转录因子的肌细胞增强因子2(MEF2)家族成员在转染的成纤维细胞中不能诱导肌生成,但当与肌源性碱性螺旋-环-螺旋(bHLH)蛋白MyoD或肌细胞生成素共表达时,它们能显著提高肌源性转化的程度,高于单独使用任何一种肌源性bHLH因子时的情况。这种协同作用需要MEF2的DNA结合结构域与肌源性bHLH因子之间直接相互作用,但只有其中一个因子需要转录激活结构域,且只有其中一个因子需要与DNA结合。这些相互作用使任一因子都能通过另一个因子的结合位点激活转录,并揭示了一种通过异源转录因子类别的DNA结合结构域之间的蛋白质-蛋白质相互作用间接激活基因表达的新机制。