III类β -微管蛋白在P19胚胎癌细胞神经元分化过程中的表达及翻译后修饰。

N B Laferrière, D L Brown
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引用次数: 30

摘要

我们使用免疫荧光显微镜、northern blotting、ELISA和等电聚焦的组合来表征由维甲酸诱导沿神经元途径分化的P19胚胎癌细胞中神经元III类β -微管蛋白的表达。分化48 h后,β - iii微管蛋白mRNA明显表达,β - iii微管蛋白出现在神经母细胞有丝分裂纺锤体中。神经突在第3天明显生长,β - iii微管蛋白和mRNA水平同时增加,直到大约第7天,β - iii mRNA水平开始下降,而蛋白质水平保持在高位。此外,在神经元分化过程中,β - iii微管蛋白亚型出现酸性增强。这些等电变异体的表达伴随着秋水仙碱稳定微管中β - iii微管蛋白水平的暂时增加。这些结果暗示了β - iii微管蛋白的翻译后修饰在P19神经元分化中微管稳定性的增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expression and posttranslational modification of class III beta-tubulin during neuronal differentiation of P19 embryonal carcinoma cells.

We have used a combination of immunofluorescence microscopy, northern blotting, ELISA, and isoelectric focusing to characterize the expression of neuronal Class III beta-tubulin in P19 embryonal carcinoma cells induced to differentiate along a neuronal pathway by retinoic acid. Following 48 h differentiation, beta-III tubulin mRNA is evident and beta-III tubulin appears in the mitotic spindle of neuroblasts. Neurite outgrowth is obvious by day 3, and beta-III tubulin protein and mRNA levels increase concurrently until approximately day 7, when beta-III mRNA levels begin to decrease while protein levels remain high. In addition, increasingly acidic beta-III tubulin isoforms appear during neuronal differentiation. The expression of these isoelectric variants occurs concomitant with a temporal increase in the levels of beta-III tubulin present in the colchicine-stable microtubules. These results implicate posttranslational modifications of beta-III tubulin in the increased microtubule stability noted in differentiating P19 neurons.

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