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PMID: 6582498 Published · ppublish English Journal Article

Preferential binding of estrogen-receptor complex to a region containing the estrogen-dependent hypomethylation site preceding the chicken vitellogenin II gene.

Jost JP, Seldran M, Geiser M

Abstract

DNA-cellulose competition binding assays were used to measure the ability of cloned DNA fragments of the chicken vitellogenin II gene to displace the estrogen-receptor complex from total chicken DNA coupled to cellulose. The DNA fragment that gave the highest competition is situated in the upstream region of the gene between nucleotides -458 and -725. This DNA fragment has four small clusters of A + T-rich sequences and contains the estrogen-dependent hypomethylation site. In vitro methylation of the Msp I site does not change the capacity of the DNA fragment to compete for estrogen-receptor complex, whereas cleavage of the C-C-G-G (Msp I site) results in a complete loss of competition of this fragment for estrogen-receptor complex. These results, combined with deoxyribonuclease I protection experiments, suggest that the most probable binding site for estrogen-receptor complex is . . .G-C-G-T-G-A-C-C-G-G-A-G-C-T-G-A-A-A-G-A-A-C-A-C. . . . This sequence has 73% homology with the core enhancer sequence of simian virus 40, . . .G-G-T-G-T-G-G-A-A-A-G. . . (identical bases italicized).

MeSH Terms
Animals Base Sequence Binding Sites Chickens Deoxyribonucleases Female Gene Expression Regulation Genes Lipoproteins/genetics Methylation Oviducts/physiology Receptors, Estrogen/genetics Seasons Vitellogenins/genetics
Chemicals
Lipoproteins Receptors, Estrogen Vitellogenins Deoxyribonucleases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Jost J P
Seldran M
Geiser M
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20 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1984-01-00
Pages
429-33
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC344690
Subset
IM
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