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Transformation of NIH 3T3 cells by a human c-sis cDNA clone.

Authors :
Clarke MF
Westin E
Schmidt D
Josephs SF
Ratner L
Wong-Staal F
Gallo RC
Reitz MS Jr
Source :
Nature [Nature] 1984 Mar 29-Apr 4; Vol. 308 (5958), pp. 464-7.
Publication Year :
1984

Abstract

The mechanism of leukaemogenic transformation by human T-cell leukaemia/lymphoma virus (HTLV), a retrovirus implicated in the aetiology of certain adult T-cell leukaemias and lymphomas, is unknown but is conceivably associated with the expression of the cellular analogues of retroviral oncogenes. The HUT-102 cell line, derived from a cutaneous T-cell lymphoma and infected with HTLV, expresses several cellular oncogenes. It is unusual among haemopoietic cell lines in that one of these is c-sis, the gene from which the oncogene v-sis of the simian sarcoma virus was derived, and perhaps the gene for platelet-derived growth factor (PDGF). To explore the possible role of c-sis expression in HTLV-induced disease, we have obtained cDNA clones of c-sis from HUT-102 cells. Here we describe two such clones and report that one of them transforms NIH-3T3 cells. This is the first example of transformation of NIH-3T3 cells by a human onc gene other than c-ras or Blym, as well as the first demonstration of transformation by a human cDNA clone.

Details

Language :
English
ISSN :
0028-0836
Volume :
308
Issue :
5958
Database :
MEDLINE
Journal :
Nature
Publication Type :
Academic Journal
Accession number :
6323994
Full Text :
https://doi.org/10.1038/308464a0