Pagnani M, Negrini M, Reschiglian P, Corallini A, Balboni P G, Scherneck S, Macino G, Milanesi G, Barbanti-Brodano G
J Virol. 1986 Aug;59(2):500-5. doi: 10.1128/JVI.59.2.500-505.1986.
We describe the molecular and biological properties of BK virus (BKV)-IR, a new BKV variant isolated from a human tumor of pancreatic islets. BKV-IR bears a 253-base-pair (bp) deletion and an 80-bp insertion in the early region of the genome. The deletion abolishes the expression of small-t antigen. The inserted sequences, grouped in four clusters, produce rearrangements in the first and second enhancer elements. They are bound by 12-bp direct repeats and could form a 217-base stem-loop structure suggestive of an insertion sequence. As compared with wild-type BKV, BKV-IR transformed hamster cells with a reduced efficiency and induced ependymomas in hamsters at a lower frequency and with a longer latency period. Tumors induced by BKV-IR, however, showed features of higher malignancy. The possible role of the insertion sequence-like element in transformation by BKV-IR is discussed.
我们描述了从人类胰岛肿瘤中分离出的一种新型BK病毒(BKV)变体——BKV-IR的分子和生物学特性。BKV-IR在基因组早期区域有一个253个碱基对(bp)的缺失和一个80 bp的插入。该缺失消除了小t抗原的表达。插入序列分为四个簇,在第一和第二增强子元件中产生重排。它们由12 bp的直接重复序列结合,可形成一个217个碱基的茎环结构,提示为插入序列。与野生型BKV相比,BKV-IR转化仓鼠细胞的效率降低,在仓鼠中诱发室管膜瘤的频率较低且潜伏期较长。然而,由BKV-IR诱导的肿瘤显示出更高的恶性特征。讨论了插入序列样元件在BKV-IR转化中的可能作用。