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Phosphatidylethanolamine N ‐methyltransferase (PEMT) gene expression is induced by estrogen in human and mouse primary hepatocytes
Author(s) -
Resseguie Mary,
Song Jiannan,
Niculescu Mihai D.,
Costa Kerry-Ann,
Randall Thomas A.,
Zeisel Steven H.
Publication year - 2007
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fj.07-8227com
Subject(s) - biology , estrogen , promoter , transcription (linguistics) , gene , gene expression , methyltransferase , alternative splicing , rna splicing , transcription factor , endocrinology , microbiology and biotechnology , genetics , messenger rna , methylation , rna , linguistics , philosophy
Choline is an essential nutrient for humans, though some of the requirement can be met by endogenous synthesis catalyzed by phosphatidylethanolamine A‐methyltransferase (PEMT). Premenopausal women are relatively resistant to choline deficiency compared with postmenopausal women and men. Studies in animals suggest that estrogen treatment can increase PEMT activity. In this study we investigated whether the PEMT gene is regulated by estrogen. PEMT transcription was increased in a dose‐dependent manner when primary mouse and human hepatocytes were treated with 17‐β‐estradiol for 24 h. This increased message was associated with an increase in protein expression and enzyme activity. In addition, we report a region that contains a perfect estrogen response element (ERE) ~7.5 kb from the transcription start site corresponding to transcript variants NM_007169 and NM‐008819 of the human and murine PEMT genes, respectively, three imperfect EREs in evolutionarily conserved regions and multiple imperfect EREs in nonconserved regions in the putative promoter regions. We predict that both the mouse and human PEMT genes have three unique transcription start sites, which are indicative of either multiple promoters and/or alternative splicing. This study is the first to explore the underlying mechanism of why dietary requirements for choline vary with estrogen status in humans.—Resseguie M., Song, J., Niculescu, M. D., da Costa K., Randall, T. A., Zeisel S. H. Phosphatidylethanolamine A ‐methyltrans‐ferase (PEMT) gene expression is induced by estrogen in human and mouse primary hepatocytes. FASEB J. 21, 2622–2632 (2007)