Wang Y, Loomis P A, Zinkowski R P, Binder L I
Department of Cell Biology, School of Medicine and Dentistry, University of Alabama, Birmingham 35294-0005.
J Cell Biol. 1993 Apr;121(2):257-67. doi: 10.1083/jcb.121.2.257.
We previously reported the presence of the microtubule-associated protein, tau in the nuclei of primate cells in culture. The present study confirms the existence of nuclear tau in two human neuroblastoma cells lines by indirect immunofluorescence and Western blot using mAbs to tau. Northern blot analysis of poly A+ mRNA detects a novel 2-kb tau transcript coexpressed with the 6-kb message in cultured human cells and human frontal cortex. PCR and cDNA sequencing demonstrate that the 2-kb message contains the entire tau coding region. Furthermore, actinomycin D transcription inhibition experiments indicate that the 2-kb message is not derived from the 6-kb message, but instead arises from the original tau transcript. One of the human neuroblastoma cell lines examined contains both nuclear and cytoplasmic tau as assayed by both Western blot and indirect immunofluorescence. Northern blot analysis of this cell line indicates that copious amounts of the 2-kb message are present while little of the 6-kb transcript is obvious. Immunofluorescence analysis of this cell line demonstrates that the cytoplasmic tau is not localized to microtubules. Together, these results indicate that the 2-kb tau message in humans may specify tau for non-microtubule functions in both the cytoplasm and the nucleus. We hypothesize that this is accomplished via a message targeting mechanism mediated by the untranslated regions of the tau messages.
我们之前报道过,在培养的灵长类动物细胞核中存在微管相关蛋白tau。本研究通过间接免疫荧光法以及使用抗tau单克隆抗体的蛋白质免疫印迹法,证实了两种人类神经母细胞瘤细胞系中存在核tau。对聚腺苷酸加尾mRNA进行的Northern印迹分析检测到一种新的2kb tau转录本,其在培养的人类细胞和人类额叶皮质中与6kb的转录本共表达。聚合酶链反应(PCR)和cDNA测序表明,2kb的转录本包含整个tau编码区。此外,放线菌素D转录抑制实验表明,2kb的转录本并非来源于6kb的转录本,而是源自原始的tau转录本。通过蛋白质免疫印迹法和间接免疫荧光法检测发现,所检测的一种人类神经母细胞瘤细胞系同时含有核tau和胞质tau。对该细胞系进行的Northern印迹分析表明,存在大量的2kb转录本,而6kb的转录本则很少见。对该细胞系进行的免疫荧光分析表明,胞质tau并不定位于微管。这些结果共同表明,人类中2kb的tau转录本可能为细胞质和细胞核中微管以外的功能指定tau。我们推测,这是通过由tau转录本的非翻译区介导的信息靶向机制实现的。