Friedman R L, Manly S P, McMahon M, Kerr I M, Stark G R
Cell. 1984 Oct;38(3):745-55. doi: 10.1016/0092-8674(84)90270-8.
Eighteen cDNAs, cloned from interferon-treated T98G neuroblastoma cells, correspond to seven different mRNAs induced up to 40-fold by interferon. One codes for metallothionein II and another for a class I HLA. The others do not code for proteins of known sequence. In the continued presence of interferon, accumulation of the mRNAs continues for about 1 day but ceases whenever interferon is removed. Once induced, the mRNAs are stable. Synthesis of new proteins is not required for induction. The rate of transcription of one of the genes doubles 5 min after treatment with interferon and reaches a maximum by 60 min. This rate begins to fall after 4-6 hr, reaching the uninduced level by 8-12 hr. Since the mRNA continues to accumulate after 8-12 hr, posttranscriptional events must also play a role in increasing its level.
从经干扰素处理的T98G神经母细胞瘤细胞中克隆出的18个cDNA,对应于7种不同的mRNA,这些mRNA被干扰素诱导高达40倍。其中一个编码金属硫蛋白II,另一个编码I类HLA。其他的不编码已知序列的蛋白质。在持续存在干扰素的情况下,mRNA的积累持续约1天,但一旦去除干扰素就会停止。一旦被诱导,mRNA是稳定的。诱导不需要合成新的蛋白质。其中一个基因在干扰素处理后5分钟转录速率加倍,60分钟时达到最大值。4-6小时后该速率开始下降,8-12小时时降至未诱导水平。由于mRNA在8-12小时后仍继续积累,转录后事件也必定在提高其水平中发挥作用。