The overall objective of this project is to further our understanding of the mechanisms of carbohydrate regulation of gene expression. During the last several years we have demonstrated that a large number of hepatic genes are regulated by alterations in the amount of carbohydrate presented to the liver cell. The mRNA for one of these genes, mRNA-S14, has proven to be an excellent model for the study of carbohydrate responsive mRNAs. With this model we have recnetly demonstrated that carbohydrate administration rapidly induces this mRNA. Furthermore, preliminary data indicate that the induction of mRNA-S14 is associated with a rise in an intracellular nucleotide. We now propose to utilize HPLC techniques to identify this nucleotide, and demonstrate that this nucleotide is the proximate intracellular mediator of the carbohydrate effect. To acccomplish this goal we shall quantitate the temporal relationship between the synthesis of this nucleotide and the accumulation of mRNA-S14 in livers from rats given various stimuli known to induce mRNA-S14. In addition we propose to identify this nucleotide by mass spectrometry. The identified nucleotide will be added to primary hepatocyte cultures in order to demonstrate that an increase in the intracellular content of the nucleotide leads to enhanced formation of mRNA- S14. Further studies on the mechanism of carbohydrate regulation of mRNA-S14 will be performed by direct measurements of the synthesis rate of this mRNA with (3H)- Uridine and measurements of degradation rates following Actinomycin D addition to hepatocyte cultures. We shall measure the rate of accumulation of the nuclear precursor of mRNA-S14 in order to demonstrate that the carbohydrate effects occurs within the nucleus of the cell. Lastly, in order to establish the nexus between animal models and human disease we shall study carbohydrate regulation of gene expression in man by examining the spectrum of mRNAs present in peripheral mononuclear cells of diabetic patients. The studies outlined in this proposal should provide a greater understanding of the mechanisms by which alterations in carbohydrate status lead to changes in gene expression.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK032885-05
Application #
3231254
Study Section
Physiological Chemistry Study Section (PC)
Project Start
1984-04-01
Project End
1992-11-30
Budget Start
1988-12-01
Budget End
1989-11-30
Support Year
5
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Type
Schools of Medicine
DUNS #
168559177
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Ota, Yasuhiro; Mariash, Cary N (2003) Paradoxical triiodothyronine suppression of S14 transcription in permanent hepatic cell lines. Thyroid 13:437-45
Zhu, Q; Mariash, A; Margosian, M R et al. (2001) Spot 14 gene deletion increases hepatic de novo lipogenesis. Endocrinology 142:4363-70
Ercan-Fang, S; Schwartz, H L; Mariash, C N et al. (2000) Quantitative assessment of pituitary resistance to thyroid hormone from plots of the logarithm of thyrotropin versus serum free thyroxine index. J Clin Endocrinol Metab 85:2299-303
Liu, B; Li, W; Mariash, C N (1999) Two different gene elements are required for glucose regulation of S14 transcription. Mol Cell Endocrinol 148:11-9
Kirschner, L S; Mariash, C N (1999) Adipose S14 mRNA is abnormally regulated in obese subjects. Thyroid 9:143-8
Ota, Y; Mariash, A; Wagner, J L et al. (1997) Cloning, expression and regulation of the human S14 gene. Mol Cell Endocrinol 126:75-81
Walker, J D; Burmeister, L A; Mariash, A et al. (1996) Insulin increases the processing efficiency of messenger ribonucleic acid-S14 nuclear precursor. Endocrinology 137:2293-9
Sudo, Y; Mariash, C N (1996) Lowering glucose depletes a thapsigargin-sensitive calcium pool and inhibits transcription of the S14 gene. Endocrinology 137:4677-84
Harmon, J S; Mariash, C N (1996) Identification of a carbohydrate response element in rat S14 gene. Mol Cell Endocrinol 123:37-44
Sudo, Y; Mariash, C N (1994) Two glucose-signaling pathways in S14 gene transcription in primary hepatocytes: a common role of protein phosphorylation. Endocrinology 134:2532-40

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