Cóias R, Galego L, Barahona I, Rodrigues-Pousada C
Laboratório de Genética Molecular, Instituto Gulbenkian, Oeirás, Portugal.
Eur J Biochem. 1988 Aug 15;175(3):467-74. doi: 10.1111/j.1432-1033.1988.tb14218.x.
The regulation of tubulin gene expression was studied in Tetrahymena pyriformis cells during heat shock (shift from 28 degrees C to 34 degrees C). Fluorograms of two-dimensional gels of radiolabelled proteins synthesized during thermal stress revealed that tubulin synthesis is highly repressed when compared with that of exponentially growing cells. The variation in the levels of alpha and beta-tubulin mRNAs was analyzed by Northern-blot hybridization using homologous genomic probes (alpha TT and beta TT1). The results obtained show that heat shock induces a drastic and coordinate reduction in the amount of alpha and beta-tubulin mRNAs isolated from polysomes. This decrease is not due to a shift from the polysomes to the post-polysomal fraction because it was also observed when total cytoplasmic mRNAs were analyzed. Run-on transcription experiments were performed in order to examine whether repression of transcription in heat-shocked cells could explain that reduction. The results obtained show that the apparent rates of tubulin gene transcription are not significantly modified, but on the contrary increase slightly in cells heat-shocked for 15 min and 30 min. The effects of inhibitors of protein synthesis, cycloheximide and pactamycin, on the destabilization of tubulin mRNAs were tested in heat-shocked Tetrahymena cells. Our results revealed that in the presence of these inhibitors, tubulin mRNAs become more stable thus suggesting that an induced factor may be involved in the degradation of alpha and beta-tubulin mRNAs during heat shock.
在嗜热四膜虫细胞热休克期间(从28℃转移至34℃),对微管蛋白基因表达的调控进行了研究。热应激期间合成的放射性标记蛋白质的二维凝胶荧光图谱显示,与指数生长的细胞相比,微管蛋白的合成受到高度抑制。使用同源基因组探针(αTT和βTT1)通过Northern印迹杂交分析α和β微管蛋白mRNA水平的变化。获得的结果表明,热休克诱导从多核糖体分离的α和β微管蛋白mRNA数量急剧且协同减少。这种减少不是由于从多核糖体向多核糖体后部分的转移,因为在分析总细胞质mRNA时也观察到了这种情况。进行了连续转录实验,以检查热休克细胞中转录抑制是否可以解释这种减少。获得的结果表明,微管蛋白基因转录的表观速率没有明显改变,但相反,在热休克15分钟和30分钟的细胞中略有增加。在热休克的嗜热四膜虫细胞中测试了蛋白质合成抑制剂环己酰亚胺和放线菌酮对微管蛋白mRNA去稳定化的影响。我们的结果表明,在这些抑制剂存在下,微管蛋白mRNA变得更稳定,因此表明热休克期间可能有诱导因子参与α和β微管蛋白mRNA的降解。