Abstract
Endogenous retrovirus sequences are present in the genome of a wide variety of animal species. The activation of the proto oncogenes of the ras family, particularly c-Ha-ras, by either point mutation or overexpression, has been shown to be associated with a vast number of different cancers. Here we report that the insertion of a defective retrovirus in the -1 intron of rat c-Ha-ras is responsible for the activation of the gene by over 10-fold overexpression in an MNU-induced rat mammary cancer. A portion of the 3' end of the retroviral sequence is expressed as a part of the c-Ha-ras transcript in the carcinoma tissue, indicating the direct involvement of this element in the transcription of the c-Ha-ras gene. The c-Ha-ras structural gene transcribed by the promoter of the defective retroviral element can neoplastically transform the NIH 3T3 cell line upon transfection.
Original language | English |
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Pages (from-to) | 835-840 |
Number of pages | 6 |
Journal | Biochemical and Biophysical Research Communications |
Volume | 248 |
Issue number | 3 |
DOIs | |
Publication status | Published - 30-07-1998 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Biophysics
- Biochemistry
- Molecular Biology
- Cell Biology