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Induction of utrophin gene expression by heregulin in skeletal muscle cells: Role of the N-box motif and GA binding protein

机译:调蛋白在骨骼肌细胞中诱导促性腺激素基因表达:N-box基序和GA结合蛋白的作用

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The modulation of utrophin gene expression in muscle by the nerve -decrived factor agrin plausibly involves the trophic factor ARIA/ heregulin. Here we show that heregulin treatment or mouse and human cultured myotubes caused a approximately equals 2.5-fold increase in utrophin mRNA levels. Transient transfection experiments with utrophin promoter-reporter gene constructs showed that this increase resulted from an enhanced transcription of the utrophin gene. In the case of the nicotinic acetylcholine receptor delta and epsilon subunit genes, heregulin was previously reported to stimulate transcription via a conserved promoter element, the N-box, which binds the multimeric Ets-related transcription factor GA binding protein (GABP). Accordingly, site-directed mutagenesis of a single N-box motif in the utrophin gene promoter abolished the transcriptional response to heregulin. In addition, over- expression of heregulin, or of the two GABP subunits in cultured myotubes, caused an N-box-dependent increase of the utrophin promoter activity. In vivo, direct gene transfer into muscle confirmed that heregulin regulates utrophin gene expression. Finally, electrophoretic mobility shift assays and supershift experiments performed with muscle extracts revealed that the N-box of the utrophin promoter binds GABP. These findings suggest that the subsynaptic activation of transcription by heregulin via the N-box motif and GABP are conserved among genes expressed at the neuromuscular junction. Because utrophin can functionally compensate for the lack of dystrophin, the elucidation of the m
机译:神经衍生因子凝集素对肌肉中促性腺激素基因表达的调节可能涉及营养因子ARIA /调蛋白。在这里,我们显示heregulin治疗或小鼠和人类培养的肌管引起的促卵泡素mRNA水平升高约等于2.5倍。用促肾上腺皮质激素启动子-报告基因基因构建体进行的瞬时转染实验表明,这种增加是由于促肾上腺皮质激素基因的转录增强所致。在烟碱乙酰胆碱受体δ和ε亚基基因的情况下,以前曾报道过调蛋白通过保守的启动子元件N-box刺激转录,所述启动子元件结合多聚体Ets相关转录因子GA结合蛋白(GABP)。因此,在促卵磷脂基因启动子中单个N-box基序的定点诱变消除了对调蛋白的转录反应。另外,调蛋白或培养的肌管中两个GABP亚基的过度表达引起了依赖于N-box的促卵磷脂启动子活性的增加。在体内,直接基因转移到肌肉中证实了调蛋白调节卵磷脂的基因表达。最后,用肌肉提取物进行的电泳迁移率迁移测定和超迁移实验表明,促卵磷脂启动子的N盒与GABP结合。这些发现表明在神经肌肉连接处表达的基因中,调蛋白通过N-box基序和GABP的突触激活被保守。由于卵磷脂可以在功能上补偿肌营养不良蛋白的缺乏,因此

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