Summerhill E M, Wood K, Fishman M C
Brain Res. 1987 Jul;388(2):99-103. doi: 10.1016/s0006-8993(87)80002-1.
Differentiation of N1E-115 neuroblastoma cells into neuron-like cells, with extension of neurites and acquisition of excitable membranes, can be induced by dimethyl sulfoxide (DMSO). We have found this differentiation to be accompanied by an increase in tyrosine hydroxylase (TH) mRNA, an increase disproportionate to changes in mRNAs for other measured, non-neuron-specific genes. The mRNA increases slowly over several days and falls gradually after removal of DMSO. Nuclear run-on studies suggest that a change in the rate of transcription cannot explain the increase in steady-state mRNA levels. TH mRNA half-life does, however, increase. This suggests that regulation is exerted in this case not at the level of transcription but rather at that of mRNA stability.
二甲基亚砜(DMSO)可诱导N1E - 115神经母细胞瘤细胞分化为神经元样细胞,使其长出神经突并获得可兴奋膜。我们发现这种分化伴随着酪氨酸羟化酶(TH)mRNA的增加,其增加幅度与其他所测非神经元特异性基因的mRNA变化不成比例。mRNA在几天内缓慢增加,去除DMSO后逐渐下降。核转录实验表明,转录速率的变化无法解释稳态mRNA水平的增加。然而,TH mRNA的半衰期确实增加了。这表明在这种情况下,调控并非发生在转录水平,而是发生在mRNA稳定性水平。