Superactive estrogen receptors. Potent activators of gene expression
- PMID: 2164005
Superactive estrogen receptors. Potent activators of gene expression
Abstract
We have constructed novel chimeric receptors consisting of the activation region of the herpes simplex virus transcription factor VP16 inserted into the amino-terminal region of the human estrogen receptor containing or lacking the hormone-binding region. By gene transfer into mammalian cells, these chimeric receptors behave in a hormone-dependent or hormone-independent manner, respectively, and are more efficient activators of gene expression than wild-type estrogen receptor. These studies indicate that a potent activation region from a viral transcription factor can be placed under hormonal control when introduced into a steroid receptor molecule and can enhance the receptor's potency (approximately 10-fold) in activating specific gene expression. It is likely that such chimeric molecules could be designed to increase selected target gene responses to any intracellular receptor in the course of cellular transfection, transformation, or transgenic animal experiments.
Similar articles
-
High efficiency transient expression of eukaryotic genes: use of an HSV-1 immediate early promoter (ICP4).Biotechniques. 1990 Aug;9(2):168-73. Biotechniques. 1990. PMID: 2169263
-
Characterization of a temperature-sensitive mutation in the hormone binding domain of the human estrogen receptor. Studies in cell extracts and intact cells and their implications for hormone-dependent transcriptional activation.J Biol Chem. 1992 May 15;267(14):9868-73. J Biol Chem. 1992. PMID: 1577818
-
The RR1 gene of herpes simplex virus type 1 is uniquely trans activated by ICP0 during infection.J Virol. 1993 Oct;67(10):6125-35. doi: 10.1128/JVI.67.10.6125-6135.1993. J Virol. 1993. PMID: 8396674 Free PMC article.
-
The human estrogen receptor has two independent nonacidic transcriptional activation functions.Cell. 1989 Nov 3;59(3):477-87. doi: 10.1016/0092-8674(89)90031-7. Cell. 1989. PMID: 2805068
-
Different regions of the estrogen receptor are required for synergistic action with the glucocorticoid and progesterone receptors.Mol Cell Biol. 1989 Dec;9(12):5324-30. doi: 10.1128/mcb.9.12.5324-5330.1989. Mol Cell Biol. 1989. PMID: 2586523 Free PMC article.
Cited by
-
Influence of the v-Myb transactivation domain on the oncoprotein's transformation specificity.EMBO J. 1993 Apr;12(4):1333-41. doi: 10.1002/j.1460-2075.1993.tb05778.x. EMBO J. 1993. PMID: 8467793 Free PMC article.
-
Examination of the DNA-binding ability of estrogen receptor in whole cells: implications for hormone-independent transactivation and the actions of antiestrogens.Mol Cell Biol. 1992 Oct;12(10):4531-8. doi: 10.1128/mcb.12.10.4531-4538.1992. Mol Cell Biol. 1992. PMID: 1406642 Free PMC article.
-
Identification of a negative regulatory function for steroid receptors.Proc Natl Acad Sci U S A. 1992 Nov 15;89(22):10563-7. doi: 10.1073/pnas.89.22.10563. Proc Natl Acad Sci U S A. 1992. PMID: 1438251 Free PMC article.
-
Antiestrogen can establish nonproductive receptor complexes and alter chromatin structure at target enhancers.Proc Natl Acad Sci U S A. 1991 Apr 15;88(8):3125-9. doi: 10.1073/pnas.88.8.3125. Proc Natl Acad Sci U S A. 1991. PMID: 2014231 Free PMC article.
-
Estradiol-inducible squelching and cell growth arrest by a chimeric VP16-estrogen receptor expressed in Saccharomyces cerevisiae: suppression by an allele of PDR1.Mol Cell Biol. 1993 Jan;13(1):462-72. doi: 10.1128/mcb.13.1.462-472.1993. Mol Cell Biol. 1993. PMID: 8417344 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources