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首页> 外文期刊>Molecular and Cellular Biology >The 2′-5′ Oligoadenylate/RNase L/RNase L Inhibitor Pathway Regulates Both MyoD mRNA Stability and Muscle Cell Differentiation
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The 2′-5′ Oligoadenylate/RNase L/RNase L Inhibitor Pathway Regulates Both MyoD mRNA Stability and Muscle Cell Differentiation

机译:2'-5'寡腺苷酸/ RNase L / RNase L抑制剂途径调节MyoD mRNA稳定性和肌肉细胞分化

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The 2′-5′ oligoadenylate (2-5A)/RNase L pathway is one of the enzymatic pathways induced by interferon. RNase L is a latent endoribonuclease which is activated by 2-5A and inhibited by a specific protein known as RLI (RNase L inhibitor). This system has an important role in regulating viral infection. Additionally, variations in RNase L activity have been observed during cell growth and differentiation but the significance of the 2-5A/RNase L/RLI pathway in these latter processes is not known. To determine the roles of RNase L and RLI in muscle differentiation, C2 mouse myoblasts were transfected with sense and antisense RLI cDNA constructs. Importantly, the overexpression of RLI in C2 cells was associated with diminished RNase L activity, an increased level of MyoD mRNA, and accelerated kinetics of muscle differentiation. Inversely, transfection of the RLI antisense construct was associated with increased RNase L activity, a diminished level of MyoD mRNA, and delayed differentiation. In agreement with these data, MyoD mRNA levels were also decreased in C2 cells transfected with an inducible RNase L construct. The effect of RNase L activity on MyoD mRNA levels was relatively specific because expression of several other mRNAs was not altered in C2 transfectants. Therefore, RNase L is directly involved in myoblast differentiation, probably through its role in regulating MyoD stability. This is the first identification of a potential mRNA target for RNase L.
机译:2'-5'寡腺苷酸(2-5A)/ RNase L途径是干扰素诱导的酶促途径之一。 RNase L是一种潜在的核糖核酸内切酶,可被2-5A激活并被称为RLI(RNase L抑制剂)的特定蛋白抑制。该系统在调节病毒感染中具有重要作用。另外,在细胞生长和分化过程中已经观察到RNase L活性的变化,但是在后面的过程中2-5A / RNase L / RLI途径的重要性尚不清楚。为了确定RNase L和RLI在肌肉分化中的作用,用有义和反义RLI cDNA构建体转染了C2小鼠成肌细胞。重要的是,R2在C2细胞中的过表达与RNase L活性降低,MyoD mRNA水平升高和肌肉分化动力学加快有关。相反,RLI反义构建体的转染与RNase L活性增加,MyoD mRNA水平降低和分化延迟有关。与这些数据一致,在用诱导型RNase L构建体转染的C2细胞中,MyoD mRNA水平也降低了。 RNase L活性对MyoD mRNA水平的影响相对特异性,因为在C2转染子中其他几种mRNA的表达没有改变。因此,RNase L可能直接通过其调控MyoD稳定性的作用直接参与成肌细胞的分化。这是对RNase L的潜在mRNA靶标的首次鉴定。

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