Saitoh O, Olson E N, Periasamy M
Department of Biochemistry & Molecular Biology, M. D. Anderson Cancer Center, University of Texas, Houston 77030.
J Biol Chem. 1990 Nov 15;265(32):19381-4.
During muscle development, muscle-specific gene expression is achieved by a complex set of transcriptional and post-transcriptional mechanisms. We examined the requirement of new protein synthesis and myogenin expression for muscle-specific tropomyosin expression during myogenesis of the rat muscle cell line L6E9. The results show that new protein synthesis is required for both muscle gene transcription and muscle-specific alternate RNA processing. However, once initiated, the synthesis of muscle tropomyosin mRNA continued in the presence of cycloheximide, while the expression of muscle actin, myosin heavy chain, and myogenin mRNA was abolished. These results suggest that muscle-specific processing of tropomyosin transcripts can continue to occur in the absence of myogenin expression unlike the expression of muscle actin and myosin heavy chain mRNAs. However, the transfection of myogenin cDNA into nonmuscle cells induced muscle-specific RNA processing of tropomyosin, suggesting indirect involvement of myogenic factors in the initiation of muscle-specific RNA processing pathways.
在肌肉发育过程中,肌肉特异性基因表达是通过一系列复杂的转录和转录后机制实现的。我们研究了大鼠肌肉细胞系L6E9成肌过程中,新蛋白质合成和肌细胞生成素表达对肌肉特异性原肌球蛋白表达的需求。结果表明,新蛋白质合成对于肌肉基因转录和肌肉特异性可变RNA加工都是必需的。然而,一旦启动,在放线菌酮存在的情况下,肌肉原肌球蛋白mRNA的合成仍在继续,而肌肉肌动蛋白、肌球蛋白重链和肌细胞生成素mRNA的表达则被消除。这些结果表明,与肌肉肌动蛋白和肌球蛋白重链mRNA的表达不同,在没有肌细胞生成素表达的情况下,原肌球蛋白转录本的肌肉特异性加工仍可继续发生。然而,将肌细胞生成素cDNA转染到非肌肉细胞中可诱导原肌球蛋白的肌肉特异性RNA加工,这表明肌源性因子间接参与了肌肉特异性RNA加工途径的启动。