Chakraborty T, Olson E N
Department of Biochemistry and Molecular Biology, University of Texas M.D. Anderson Cancer Center, Houston 77030.
Mol Cell Biol. 1991 Dec;11(12):6103-8. doi: 10.1128/mcb.11.12.6103-6108.1991.
Myogenin and MRF4 belong to the MyoD family of muscle-specific transcription factors, which can activate myogenesis when introduced into nonmyogenic cells. These proteins share homology within a basic-helix-loop-helix motif that mediates DNA binding and dimerization, but they are divergent in their amino and carboxyl termini. Although myogenin and MRF4 bind the same sequence within the muscle creatine kinase enhancer, only myogenin efficiently transactivates this enhancer. By creating chimeras of myogenin and MRF4, we show that the specificities of these factors for transactivation of the muscle creatine kinase enhancer can be interchanged by swapping their amino and carboxyl termini. Within these chimeras, strong cooperation between the amino and carboxyl termini was observed. These findings suggest that myogenin and MRF4 discriminate between muscle-specific enhancers and that target gene specificity is determined by domains surrounding the basic-helix-loop-helix region.
肌细胞生成素(Myogenin)和MRF4属于肌肉特异性转录因子的MyoD家族,当被导入非肌源性细胞时,它们能够激活肌细胞生成。这些蛋白质在介导DNA结合和二聚化的碱性螺旋-环-螺旋基序内具有同源性,但它们在氨基末端和羧基末端存在差异。尽管肌细胞生成素和MRF4结合肌肉肌酸激酶增强子内的相同序列,但只有肌细胞生成素能有效地反式激活该增强子。通过构建肌细胞生成素和MRF4的嵌合体,我们发现通过交换它们的氨基末端和羧基末端,可以互换这些因子对肌肉肌酸激酶增强子反式激活的特异性。在这些嵌合体内,观察到氨基末端和羧基末端之间有强烈的协同作用。这些发现表明,肌细胞生成素和MRF4能够区分肌肉特异性增强子,并且靶基因特异性由碱性螺旋-环-螺旋区域周围的结构域决定。