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Structural organization and expression of the mouse estrogen receptor
1Molecular Endocrinology Laboratory, Imperial Cancer Research Fund, United Kingdom.
Molecular Endocrinology (Baltimore, Md.)
|October 1, 1987
Summary
Researchers isolated and characterized mouse uterus estrogen receptor complementary DNA (cDNA) clones. Functional assays confirmed the estrogen receptor
Area of Science:
- Molecular Biology
- Endocrinology
- Genetics
Background:
- Estrogen receptors (ERs) are crucial for reproductive health and development.
- Understanding the mouse ER provides insights into mammalian estrogen signaling.
Purpose of the Study:
- To isolate and characterize complementary DNA (cDNA) clones for the mouse uterus estrogen receptor.
- To investigate the expression and functional properties of the mouse estrogen receptor.
Main Methods:
- Nucleotide sequence analysis of cDNA clones.
- Isolation of genomic clones using cosmid libraries.
- Gene expression analysis via RNase mapping, primer extension, and Northern blotting.
- Functional verification through cell transfection assays (COS-1 cells).
Main Results:
- Mouse estrogen receptor cDNA predicts a 599-amino acid polypeptide with high homology to other species.
- Transcription initiates at multiple sites, producing a ~6.5 kb mRNA.
- Transfected mouse estrogen receptor confers estradiol-stimulated reporter gene activity.
- Tamoxifen and 4-hydroxytamoxifen exhibit antiestrogenic activity in vitro.
Conclusions:
- The study provides a comprehensive characterization of the mouse estrogen receptor.
- Demonstrates functional activity and differential response to antiestrogens in vitro.
- Establishes a foundation for further research into estrogen receptor-mediated pathways in mice.