Content J, De Wit L, Tavernier J, Fiers W
Nucleic Acids Res. 1983 May 11;11(9):2627-38. doi: 10.1093/nar/11.9.2627.
Northern blot analysis reveals that total RNA from human fibroblastoid cells (MG 63) induced with poly(I).poly(C) under conditions of IFN-beta production, contains predominantly a +/- 1,200 nucleotide long poly (A) mRNA (mRNA.M) which hybridizes with a Hu IFN-beta cDNA specific probe. But hybridization with this probe also enabled the detection of a polyadenylated RNA (RNA.I) with a length of between 3.5 kb-3.8 kb, representing 0.6% of the total hybridizable cellular RNA in superinduced cells. Mapping shows that the RNA.I contains all the sequence information present in mRNA.M. Furthermore, it also hybridizes to sequences, located downstream from the IFN-beta gene up to 2.5 kb beyond its poly A attachment site, while no hybridization to fragments located upstream of the IFN-beta mRNA cap site was observable. Hence this RNA.I corresponds to a transcript that starts at the same position as the major mRNA.M but which extends up to 2.5 kb beyond the 3'-end of mRNA.M where another polyadenylation signal is located.
Northern印迹分析显示,在产生IFN-β的条件下,用聚肌苷酸-聚胞苷酸(poly(I).poly(C))诱导的人成纤维样细胞(MG 63)的总RNA,主要包含一种长度约为1200个核苷酸的带poly(A)的mRNA(mRNA.M),它能与Hu IFN-β cDNA特异性探针杂交。但与该探针杂交还能检测到一种长度在3.5 kb至3.8 kb之间的聚腺苷酸化RNA(RNA.I),在超诱导细胞中它占可杂交细胞总RNA的0.6%。图谱分析表明,RNA.I包含mRNA.M中存在的所有序列信息。此外,它还能与位于IFN-β基因下游直至其poly A加尾位点下游2.5 kb处的序列杂交,而未观察到与IFN-β mRNA帽位点上游片段的杂交。因此,这种RNA.I对应于一种转录本,其起始位置与主要的mRNA.M相同,但延伸至mRNA.M 3'端以外2.5 kb处,此处存在另一个聚腺苷酸化信号。