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在肌源性分化过程中Tis11B基因的强烈诱导。

Strong induction of the Tis11B gene in myogenic differentiation.

作者信息

Busse Melanie, Schwarzburger Max, Berger Felicitas, Hacker Christine, Munz Barbara

机构信息

Institute of Physiology, Charité - University Medicine Berlin, Arnimallee 22, D-14195 Berlin, Germany.

出版信息

Eur J Cell Biol. 2008 Jan;87(1):31-8. doi: 10.1016/j.ejcb.2007.07.005. Epub 2007 Sep 24.

Abstract

TIS11B is a zinc-finger protein of the tristetraprolin (TTP) family. Using cDNA microarray analysis, we could identify the Tis11B gene based on its differential expression in myogenesis. Here, we demonstrate that expression of the Tis11B gene is strongly induced during differentiation of the murine myoblast cell line C2C12. By contrast, expression of Ttp itself was not induced in myogenesis. Pretreatment of the cells with the translation inhibitor cycloheximide demonstrated that Tis11B was a primary response gene in this process. In addition, pretreatment with the transcription inhibitor actinomycin D demonstrated that gene expression was regulated at the transcriptional level. Since specific inhibitors of p38 MAP kinase completely blocked Tis11B induction, we conclude that expression of the Tis11B gene is regulated at least in part by this signaling pathway which plays a central role in myogenesis. Induction of Tis11B expression was also observed in primary myoblasts isolated from two different mouse strains, indicating physiological relevance of our results. In addition, TIS11B might also be an important player during myogenic differentiation and regeneration in vivo, as we detected a marked decrease in expression in several muscle tissues of the dystrophic mdx mouse, a model for continuous muscle degeneration and regeneration. These data suggest that TIS11B is an important regulator of myogenesis.

摘要

TIS11B是三指四脯氨酸(TTP)家族的一种锌指蛋白。通过cDNA微阵列分析,我们能够基于其在肌生成中的差异表达来鉴定Tis11B基因。在此,我们证明在小鼠成肌细胞系C2C12分化过程中Tis11B基因的表达被强烈诱导。相比之下,Ttp自身的表达在肌生成中未被诱导。用翻译抑制剂环己酰亚胺对细胞进行预处理表明Tis11B是此过程中的一个初级反应基因。此外,用转录抑制剂放线菌素D进行预处理表明基因表达在转录水平受到调控。由于p38丝裂原活化蛋白激酶的特异性抑制剂完全阻断了Tis11B的诱导,我们得出结论,Tis11B基因的表达至少部分受该在肌生成中起核心作用的信号通路调控。在从两种不同小鼠品系分离的原代成肌细胞中也观察到了Tis11B表达的诱导,这表明我们结果具有生理相关性。此外,TIS11B在体内肌生成分化和再生过程中可能也是一个重要参与者,因为我们在营养不良性mdx小鼠(一种持续肌肉退化和再生的模型)的多个肌肉组织中检测到其表达显著下降。这些数据表明TIS11B是肌生成的一个重要调节因子。

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