Journal of Nutrition LabDiet, Your World of Nutritional Answers

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Rowling, M. J.
Right arrow Articles by Schalinske, K. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rowling, M. J.
Right arrow Articles by Schalinske, K. L.
© 2002 The American Society for Nutritional Sciences J. Nutr. 132:365-369, 2002


Nutrient-Gene Expression

Vitamin A and Its Derivatives Induce Hepatic Glycine N-Methyltransferase and Hypomethylation of DNA in Rats1

Matthew J. Rowling, Mary H. McMullen and Kevin L. Schalinske2

Department of Food Science and Human Nutrition, Iowa State University, Ames, IA 50011

2To whom correspondence should be addressed. E-mail: kschalin{at}iastate.edu.

Regulation of S-adenosylmethionine (SAM) and the SAM/S-adenosylhomocysteine (SAH) ratio by the key cytosolic enzyme glycine N-methyltransferase (GNMT) is essential in optimizing methyl group supply and subsequent functioning of methyltransferase enzymes. Therefore, inappropriate activation of GNMT may lead to the loss of methyl groups vital for many SAM-dependent transmethylation reactions. Previously, we demonstrated that the retinoid derivatives 13-cis- (CRA) and all-trans-retinoic acid (ATRA) mediated both the activity of GNMT and its abundance. The present study was conducted to determine whether vitamin A had a similar ability to up-regulate GNMT and to assess the biological importance of GNMT modulation by examining both the transmethylation and transsulfuration pathways after retinoid treatment. Rats were fed a control (10% casein + 0.3% L-methionine) diet and orally given retinyl palmitate (RP), CRA, ATRA or vehicle daily for 10 d. RP, CRA and ATRA elevated hepatic GNMT activity 32, 74 and 124%, respectively, compared with the control group. Moreover, the retinoid-mediated changes in GNMT activity were reflected in GNMT abundance (38, 89 and 107% increases for RP-, CRA-, and ATRA-treated rats, respectively). In addition, hepatic DNA, a substrate for SAM-dependent transmethylation, was hypomethylated (~100%) after ATRA treatment compared with the control group. In contrast, the transsulfuration product glutathione was unaffected by retinoid treatment. These results provide evidence of the following: 1) vitamin A, like its retinoic acid derivatives, can induce enzymatically active GNMT; and 2) inappropriate induction of GNMT can lead to a biologically important loss of methyl groups and the subsequent impairment of essential transmethylation processes.


KEY WORDS: S-adenosylmethionine • glycine N-methyltransferase • vitamin A • hypomethylation • rats




This article has been cited by other articles:


Home page
Clin. Cancer Res.Home page
Y.-C. Huang, C.-M. Lee, M. Chen, M.-Y. Chung, Y.-H. Chang, W. J.-S. Huang, D. M.-T. Ho, C.-C. Pan, T. T. Wu, S. Yang, et al.
Haplotypes, Loss of Heterozygosity, and Expression Levels of Glycine N-Methyltransferase in Prostate Cancer
Clin. Cancer Res., March 1, 2007; 13(5): 1412 - 1420.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
B. Beagle, T. L. Yang, J. Hung, E. A. Cogger, D. J. Moriarty, and M. A. Caudill
The Glycine N-Methyltransferase (GNMT) 1289 C->T Variant Influences Plasma Total Homocysteine Concentrations in Young Women after Restricting Folate Intake
J. Nutr., December 1, 2005; 135(12): 2780 - 2785.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
C. L. Ulrey, L. Liu, L. G. Andrews, and T. O. Tollefsbol
The impact of metabolism on DNA methylation
Hum. Mol. Genet., April 15, 2005; 14(suppl_1): R139 - R147.
[Abstract] [Full Text] [PDF]


Home page
Exp. Biol. Med.Home page
C. D. Davis and E. O. Uthus
DNA Methylation, Cancer Susceptibility, and Nutrient Interactions
Experimental Biology and Medicine, November 1, 2004; 229(10): 988 - 995.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
K. A. Tanghe, T. A. Garrow, and K. L. Schalinske
Triiodothyronine Treatment Attenuates the Induction of Hepatic Glycine N-Methyltransferase by Retinoic Acid and Elevates Plasma Homocysteine Concentrations in Rats
J. Nutr., November 1, 2004; 134(11): 2913 - 2918.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
K. M. Nieman, M. J. Rowling, T. A. Garrow, and K. L. Schalinske
Modulation of Methyl Group Metabolism by Streptozotocin-induced Diabetes and All-trans-retinoic Acid
J. Biol. Chem., October 29, 2004; 279(44): 45708 - 45712.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
S.-Y. Chen, J.-R. V. Lin, R. Darbha, P. Lin, T.-Y. Liu, and Y.-M. A. Chen
Glycine N-Methyltransferase Tumor Susceptibility Gene in the Benzo(a)pyrene-Detoxification Pathway
Cancer Res., May 15, 2004; 64(10): 3617 - 3623.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
M. K. Ozias and K. L. Schalinske
All-trans-Retinoic Acid Rapidly Induces Glycine N-methyltransferase in a Dose-Dependent Manner and Reduces Circulating Methionine and Homocysteine Levels in Rats
J. Nutr., December 1, 2003; 133(12): 4090 - 4094.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
M. J. Rowling and K. L. Schalinske
Retinoic Acid and Glucocorticoid Treatment Induce Hepatic Glycine N-Methyltransferase and Lower Plasma Homocysteine Concentrations in Rats and Rat Hepatoma Cells
J. Nutr., November 1, 2003; 133(11): 3392 - 3398.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
M. J. Rowling, M. H. McMullen, D. C. Chipman, and K. L. Schalinske
Hepatic Glycine N-Methyltransferase Is Up-Regulated by Excess Dietary Methionine in Rats
J. Nutr., September 1, 2002; 132(9): 2545 - 2550.
[Abstract] [Full Text] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
Copyright © 2002 by American Society for Nutrition