Abstract |
The effects of estrogen treatment on rat prolactin (PRL) gene methylation were analyzed in normal pituitaries and in three transplantable rat pituitary tumors. Northern analysis showed increased PRL mRNA expression in estrogen-treated pituitary and in MtT/F4 and MtT/ F-DMBA tumors. Prolactin mRNA amounts in MtT/W15 tumor were decreased by estrogen treatment. There was an inverse relationship between changes in PRL mRNA expression and changes in gene methylation in the coding regions of the PRL gene after estrogen treatment. The amounts of the 4.6-Kb and 1.8-Kb restriction fragments generated by HpaII digestion in pituitary tissues were influenced by estrogen, with an increase in these fragments in normal pituitary, MtT/F4, and MtT/ F-DMBA tumors after estrogen treatment. In contrast, the amounts of the 4.6-Kb and 1.8-Kb fragments were decreased in MtT/W15 tumors after estrogen treatment. Most of the internal -CCGG- sites in the PRL gene were methylated in the liver, and the PRL gene was not expressed in the liver. These data suggest that there is a tissue-specific pattern of DNA methylation of the PRL gene and that PRL gene methylation is influenced by estrogen in vivo in normal and tumorous pituitary tissues. These results also suggest that estrogen may influence PRL expression by multiple mechanisms, including changes in the level of DNA methylation.
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Authors | E Kulig, T D Landefeld, R V Lloyd |
Journal | The American journal of pathology
(Am J Pathol)
Vol. 140
Issue 1
Pg. 207-14
(Jan 1992)
ISSN: 0002-9440 [Print] United States |
PMID | 1731525
(Publication Type: Comparative Study, Journal Article, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Estrogens
- RNA, Messenger
- Prolactin
- DNA
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Topics |
- Animals
- Blotting, Northern
- Blotting, Southern
- DNA
(metabolism)
- Estrogens
(pharmacology)
- Female
- Gene Expression Regulation
(drug effects, genetics)
- Gene Expression Regulation, Neoplastic
(drug effects, genetics)
- Genes
(genetics)
- Methylation
- Pituitary Gland
(chemistry, metabolism)
- Pituitary Neoplasms
(chemistry, metabolism)
- Prolactin
(genetics)
- RNA, Messenger
(analysis, genetics)
- Rats
- Rats, Inbred F344
- Rats, Inbred WF
- Transcription, Genetic
(drug effects)
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