Hayakawa Y, Obata K, Itoh N, Yanaihara N, Okamoto H
J Biol Chem. 1984 Jul 25;259(14):9207-11.
The mechanism of N6,O2'-dibutyryl adenosine 3':5'-monophosphate (Bt2cAMP) induction of pro-vasoactive intestinal polypeptide (VIP)/PHM-27 biosynthesis was investigated in human neuroblastoma cells in culture. When neuroblastoma cells were grown for 48 h in the presence of 1 mM Bt2cAMP, the synthesis of pro-VIP/PHM-27 was stimulated 11-fold. The amount of prepro-VIP/PHM-27 mRNA determined both by hybridization with cloned prepro-VIP/PHM-27 cDNA and a reticulocyte cell-free translation assay was also increased 11-fold in the Bt2cAMP-induced cells. Transcription of prepro-VIP/PHM-27 mRNA in isolated nuclei was observed in induced cells, but not in uninduced cells. Blot hybridization with prepro-VIP/PHM-27 cDNA of total nuclear RNA isolated from neuroblastoma cells revealed an RNA species corresponding to mature prepro-VIP/PHM-27 mRNA, and the amount of the RNA was markedly increased in the induced cells. The quantity of VIP/PHM-27 gene in the DNA of neuroblastoma cells was analyzed after hydrolysis with a restriction endonuclease, EcoRI. However, VIP/PHM-27 gene was not amplified in the induced cells. These results indicate that Bt2cAMP-induced pro-VIP/PHM-27 synthesis is achieved by enhancing the transcription rate of prepro-VIP/PHM-27 mRNA.
在培养的人神经母细胞瘤细胞中研究了N6,O2'-二丁酰腺苷3':5'-单磷酸(Bt2cAMP)诱导促血管活性肠多肽(VIP)/PHM-27生物合成的机制。当神经母细胞瘤细胞在1 mM Bt2cAMP存在下培养48小时时,促VIP/PHM-27的合成被刺激了11倍。通过与克隆的前体VIP/PHM-27 cDNA杂交和网织红细胞无细胞翻译试验测定的前体VIP/PHM-27 mRNA量在Bt2cAMP诱导的细胞中也增加了11倍。在诱导细胞中观察到分离细胞核中前体VIP/PHM-27 mRNA的转录,但在未诱导细胞中未观察到。用从神经母细胞瘤细胞分离的总核RNA的前体VIP/PHM-27 cDNA进行印迹杂交,发现一种与成熟前体VIP/PHM-27 mRNA相对应的RNA种类,并且该RNA的量在诱导细胞中明显增加。用限制性内切酶EcoRI水解后分析神经母细胞瘤细胞DNA中VIP/PHM-27基因的量。然而,VIP/PHM-27基因在诱导细胞中未扩增。这些结果表明,Bt2cAMP诱导的促VIP/PHM-27合成是通过提高前体VIP/PHM-27 mRNA的转录速率来实现的。