Abstract
Mouse mammary tumor virus (MMTV) has long been implicated in mouse mammary carcinogenesis, and it is now well established that the long terminal repeat (LTR) contains regulatory sequences responsible for glucocorticoid-mediated induction of viral RNA. However, we have demonstrated previously that androgens as well as glucocorticoids can regulate MMTV RNA in the S115 mouse mammary tumor cell line. To determine if androgens act directly on the LTR in these cells, plasmids were constructed with the MMTV LTR joined to the coding sequences of genes not normally expressed in the cells. Following transfection of these chimeric genes into S115 cells, we show that the expression of the genes is regulated by both androgens and glucocorticoids. Furthermore, hormonal regulation is also conferred by the LTR on the neighboring guanine phosphoribosyltransferase (gpt) gene. Thus, androgens can act on the LTR of MMTV when the appropriate receptors are present in the cells, and this interaction can influence the expression of additional adjacent genes.
MeSH Terms
Androgens/pharmacology
Animals
DNA Restriction Enzymes/metabolism
DNA, Viral/analysis
Dexamethasone/metabolism
Electrophoresis, Polyacrylamide Gel
Endonucleases/metabolism
Mammary Tumor Virus, Mouse/genetics
Metals/pharmacology
Mice
RNA, Viral/analysis
Repetitive Sequences, Nucleic Acid
Single-Strand Specific DNA and RNA Endonucleases
Testosterone/pharmacology
Transfection
Chemicals
Androgens
DNA, Viral
Metals
RNA, Viral
Testosterone
Dexamethasone
Endonucleases
DNA Restriction Enzymes
Single-Strand Specific DNA and RNA Endonucleases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Darbre P
Page M
King R J
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