Functional analysis of the steroid hormone control region of mouse mammary tumor virus
Open Access
- 1 January 1984
- journal article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 12 (10) , 4191-4206
- https://doi.org/10.1093/nar/12.10.4191
Abstract
Gene fusions between the mouse mammary tunor virus long terminal repeat and the E. coli lacZ gene have been shown to exhibit hormone dependent expression of β-galactosidase activity. These constructions were used in transient expression experiments to assess the effects of specific modifications introduced into the region upstream of the transcription initiation site. 5′ deletions denonstrate that sequences sufficient for wild-type promoter function are contained downstream of residue −64 relative to the initiation site. Other deletions define a region of approximately 80 base pairs between −220 arid −140 which contains sequences essential for hormonal control. Between this control region and the promoter lie sequences dispensable for both functions.Keywords
This publication has 26 references indexed in Scilit:
- [57] Sequencing end-labeled DNA with base-specific chemical cleavagesPublished by Elsevier ,2004
- In vivo sequence requirements of the SV40 early promoter regionNature, 1981
- Nucleotide sequences at host–proviral junctions for mouse mammary tumour virusNature, 1980
- Expression of a Bacterial Gene in Mammalian CellsScience, 1980
- Glucocorticoid regulation of mouse mammary tumor virus gene expressionBiochimica et Biophysica Acta (BBA) - Reviews on Cancer, 1979
- Isolation of biologically active ribonucleic acid from sources enriched in ribonucleaseBiochemistry, 1979
- Molecular Mechanisms of Steroid Hormone ActionAdvances in Cancer Research, 1978
- Sizing and mapping of early adenovirus mRNAs by gel electrophoresis of S1 endonuclease-digested hybridsCell, 1977
- Steroid Receptors: Elements for Modulation of Eukaryotic TranscriptionAnnual Review of Biochemistry, 1976
- Nucleotide sequence analysis of deoxyribonucleic acid. VII. Characterization of Escherichia coli exonuclease 3 activity for possible use in terminal nucleotide sequence analysis of duplex deoxyribonucleic acid.1972