Mori K, Sabe H, Siomi H, Iino T, Tanaka A, Takeuchi K, Hirayoshi K, Hatanaka M
J Gen Virol. 1987 Feb;68 ( Pt 2):499-506. doi: 10.1099/0022-1317-68-2-499.
We isolated the full length provirus of human T cell leukaemia virus type I (HTLV-I) from MT-2, a lymphoid cell line producing HTLV-I. In three non-lymphoid cell lines (COS7, human osteosarcoma HOS cells, and HeLa) this provirus expressed a trans-acting activity after co-transfection with a recombinant plasmid carrying a bacterial chloramphenicol acetyltransferase gene under the control of a long terminal repeat of HTLV-I provirus. The trans-acting protein p40 was detected by immunoprecipitation in transfected HOS cells. Structural proteins of HTLV-I, the gag and env products, were also formed and processed in the same manner as observed in MT-2 cells. In transfected HeLa cells, the p40 protein was mainly localized in the nucleus, while other structural proteins were detected in the cytoplasm and/or the membrane by indirect immunofluorescence. Syncytium formation was observed in HeLa cells after transfection. These results demonstrated that non-lymphoid cells could produce the major proteins of HTLV-I after DNA transfection of the cloned provirus.
我们从产生人类嗜T淋巴细胞病毒I型(HTLV-I)的淋巴样细胞系MT-2中分离出了HTLV-I的全长前病毒。在三个非淋巴样细胞系(COS7、人骨肉瘤HOS细胞和HeLa细胞)中,该前病毒与携带在HTLV-I前病毒长末端重复序列控制下的细菌氯霉素乙酰转移酶基因的重组质粒共转染后,表现出反式作用活性。通过免疫沉淀在转染的HOS细胞中检测到反式作用蛋白p40。HTLV-I的结构蛋白,即gag和env产物,也以与在MT-2细胞中观察到的相同方式形成和加工。在转染的HeLa细胞中,p40蛋白主要定位于细胞核,而通过间接免疫荧光在细胞质和/或细胞膜中检测到其他结构蛋白。转染后在HeLa细胞中观察到了合胞体形成。这些结果表明,非淋巴样细胞在克隆前病毒DNA转染后可以产生HTLV-I的主要蛋白。