Darlix J L, Khandjian E W, Weil R
Proc Natl Acad Sci U S A. 1984 Sep;81(17):5425-9. doi: 10.1073/pnas.81.17.5425.
Simian virus 40 (SV40) large tumor (T) antigen isolated from mammalian cells undergoing lytic or transforming infection is associated with small RNA fragments ("T-antigen RNA") that are protected from nuclease digestion. The rather high complexity of the ribonuclease T1 fingerprints of T-antigen RNA suggested that it is mainly derived from cellular heterogeneous nuclear RNAs. In the present study, 5'-32P-labeled T-antigen RNA was hybridized to monkey, mouse, and human Alu and SV40 DNA, and the nucleotide sequence of 37 T1 oligonucleotides was determined. The results suggest that the bulk of T-antigen RNA is derived from noncoding, double-stranded, ordered regions of cellular heterogeneous nuclear RNAs that exhibit sequence homologies with interspersed repetitive elements of the cellular genome. The possible biological implications of these results are discussed.
从经历裂解性或转化性感染的哺乳动物细胞中分离出的猿猴病毒40(SV40)大T抗原,与可抵抗核酸酶消化的小RNA片段(“T抗原RNA”)相关。T抗原RNA的核糖核酸酶T1指纹图谱相当复杂,这表明它主要来源于细胞异质性核RNA。在本研究中,将5'-32P标记的T抗原RNA与猴、小鼠和人类的Alu及SV40 DNA杂交,并测定了37个T1寡核苷酸的核苷酸序列。结果表明,大部分T抗原RNA来源于细胞异质性核RNA的非编码、双链、有序区域,这些区域与细胞基因组的散布重复元件具有序列同源性。讨论了这些结果可能的生物学意义。