TY - JOUR
T1 - Expression of a provirus of human T cell leukaemia virus type I by DNA transfection
AU - Mori, K.
AU - Sabe, H.
AU - Siomi, H.
AU - Iino, T.
AU - Tanaka, A.
AU - Takeuchi, K.
AU - Hirayoshi, K.
AU - Hatanaka, M.
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 1987
Y1 - 1987
N2 - 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 transacting 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.
AB - 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 transacting 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.
UR - http://www.scopus.com/inward/record.url?scp=0023154701&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0023154701&partnerID=8YFLogxK
U2 - 10.1099/0022-1317-68-2-499
DO - 10.1099/0022-1317-68-2-499
M3 - Article
C2 - 3029287
AN - SCOPUS:0023154701
SN - 0022-1317
VL - 68
SP - 499
EP - 506
JO - Journal of General Virology
JF - Journal of General Virology
IS - 2
ER -