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Estrogen-Responsive Element of the Human pS2 Gene is an Imperfectly Palindromic Sequence
Using chimeric recombinants transfected into HeLa cells and a transient expression assay, we demonstrate that the 5′-flanking region of the pS2 gene from position -428 to position -324 exhibits both constitutive and estrogen-inducible enhancer activity. The estrogen-inducible activity, but not the c...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 1989-02, Vol.86 (4), p.1218-1222 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Using chimeric recombinants transfected into HeLa cells and a transient expression assay, we demonstrate that the 5′-flanking region of the pS2 gene from position -428 to position -324 exhibits both constitutive and estrogen-inducible enhancer activity. The estrogen-inducible activity, but not the constitutive activity, was inhibited by antiestrogens. ICI 164,384 behaved as a pure antagonist, whereas hydroxytamoxifen was a partial agonist-antagonist. The estrogen-responsive element of the pS2 gene has been narrowed down by site-directed deletion mutagenesis to a 13-base-pair (position -405 to position -393) imperfectly palindromic sequence, which in isolation can confer estrogen inducibility to the heterologous rabbit β -globin gene promoter. On the other hand, the sequences responsible for the constitutive enhancer activity are spread over the entire region. |
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ISSN: | 0027-8424 1091-6490 |
DOI: | 10.1073/pnas.86.4.1218 |