首页> 外文期刊>Journal of cellular biochemistry. >Expression and subcellular localization of myogenic regulatory factors during the differentiation of skeletal muscle C2C12 myoblasts.
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Expression and subcellular localization of myogenic regulatory factors during the differentiation of skeletal muscle C2C12 myoblasts.

机译:骨骼肌C2C12成肌细胞分化过程中肌源性调节因子的表达和亚细胞定位。

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It is known that the MyoD family members (MyoD, Myf5, myogenin, and MRF4) play a pivotal role in the complex mechanism of skeletal muscle cell differentiation. However, fragmentary information on transcription factor-specific regulation is available and data on their post-transcriptional and post-translational behavior are still missing. In this work, we combined mRNA and protein expression analysis with their subcellular localization. Each myogenic regulator factor (MRF) revealed a specific mRNA trend and a protein quantitative analysis not overlapping, suggesting the presence of post-transcriptional mechanisms. In addition, each MRF showed a specific behavior in situ, characterized by a differentiation stage-dependent localization suggestive of a post-translational regulation also. Consistently with their transcriptional activity, immunogold electron microscopy data revealed MRFs distribution in interchromatin domains. Our results showed a MyoD and Myf5 contrasting expression profile in proliferating myoblasts, as well as myogenin and MRF4 opposite distribution in the terminally differentiated myotubes. Interestingly, MRFs expression and subcellular localization analysis during C2C12 cell differentiation stages showed two main MRFs regulation mechanisms: (i) the protein half-life regulation to modulate the differentiation stage-dependent transcriptional activity and (ii) the cytoplasmic retention, as a translocation process, to inhibit the transcriptional activity. Therefore, our results exhibit that MRFs nucleo-cytoplasmic trafficking is involved in muscle differentiation and suggest that, besides the MRFs expression level, also MRFs subcellular localization, related to their functional activity, plays a key role as a regulatory step in transcriptional control mechanisms.
机译:已知MyoD家族成员(MyoD,Myf5,myogenin和MRF4)在骨骼肌细胞分化的复杂机制中起着关键作用。但是,有关转录因子特异性调控的片段信息是可用的,有关其转录后和翻译后行为的数据仍然缺失。在这项工作中,我们结合了mRNA和蛋白质表达分析及其亚细胞定位。每个肌源性调节因子(MRF)均显示出特定的mRNA趋势和不重叠的蛋白质定量分析,表明存在转录后机制。此外,每个MRF均表现出特定的原位行为,其特征在于依赖于分化阶段的本地化,也暗示了翻译后调控。与它们的转录活性一致,免疫金电子显微镜数据显示出染色质间域中的MRF分布。我们的结果显示,在增生的成肌细胞中,MyoD和Myf5的对比表达谱以及在最终分化的肌管中的肌生成素和MRF4相反分布。有趣的是,在C2C12细胞分化阶段的MRF表达和亚细胞定位分析显示出两种主要的MRF调控机制:(i)调节蛋白的半衰期以调节分化阶段相关的转录活性,以及​​(ii)作为转运过程的胞质保留,以抑制转录活性。因此,我们的研究结果表明MRF的核质运输涉及肌肉分化,并表明,除了MRF的表达水平外,与其功能活性相关的MRF的亚细胞定位也起着关键作用,在转录控制机制中起调节作用。

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