首页> 外文期刊>Molecular biology reports >Myotonic dystrophy type 1-associated CTG repeats disturb the expression and subcellular distribution of microtubule-associated proteins MAP1A, MAP2, and MAP6/STOP in PC12 cells.
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Myotonic dystrophy type 1-associated CTG repeats disturb the expression and subcellular distribution of microtubule-associated proteins MAP1A, MAP2, and MAP6/STOP in PC12 cells.

机译:与强直性营养不良1型相关的CTG重复序列干扰了PC12细胞中微管相关蛋白MAP1A,MAP2和MAP6 / STOP的表达和亚细胞分布。

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To study the effect of DM1-associated CTG repeats on neuronal function, we developed a PC12 cell-based model that constitutively expresses the DMPK gene 3'-untranslated region with 90 CTG repeats (CTG90 cells). As CTG90 cells exhibit impaired neurite outgrowth and as microtubule-associated proteins (MAPs) are crucial for microtubule stability, we analyzed whether MAPs are a target of CTG repeats. NGF induces mRNA expression of Map2, Map1a and Map6 in control cells (PC12 cells transfected with the empty vector), but this induction is abolished for Map2 and Map1a in CTG90 cells. MAP2 and MAP6/STOP proteins decrease in NGF-treated CTG90 cells, whereas MAP1A increases. Data suggest that CTG repeats might alter somehow the expression of MAPs, which appears to be related with CTG90 cell-deficient neurite outgrowth. Decreased MAP2 levels found in the hippocampus of a DM1 mouse model indicates that targeting of MAPs expression by CTG repeats might be relevant to DM1.
机译:为了研究DM1相关的CTG重复序列对神经元功能的影响,我们开发了一种基于PC12细胞的模型,该模型可组成性表达具有90个CTG重复序列的DMPK基因3'非翻译区(CTG90细胞)。由于CTG90细胞表现出受损的神经突增生,并且由于微管相关蛋白(MAP)对于微管稳定性至关重要,因此我们分析了MAP是否是CTG重复的靶标。 NGF在对照细胞(用空载体转染的PC12细胞)中诱导Map2,Map1a和Map6的mRNA表达,但在CTG90细胞中对Map2和Map1a的诱导被取消。在NGF处理的CTG90细胞中,MAP2和MAP6 / STOP蛋白减少,而MAP1A增加。数据表明,CTG重复序列可能以某种方式改变MAPs的表达,这似乎与CTG90细胞缺陷的神经突增生有关。在DM1小鼠模型的海马体中发现的MAP2水平降低表明CTG重复靶向MAPs表达可能与DM1有关。

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