Effects of Cofactor Tetrahydrobiopterin and Deletions on the Regulatory Domain of Tyrosine Hydroxylase on the Expression of Tyrosine Hydroxylase.
- Author:
Yong Won CHO
1
;
Sang Doe YI
;
Jung Kun LIM
;
Hyung LEE
;
Yong Sik KIM
;
Uhn LEE
;
Young Jae LEE
Author Information
1. Department of Neurology, Keimyung University.
- Publication Type:In Vitro ; Original Article
- Keywords:
Parkinson's disease;
Tyrosine hydroxylase;
Regulatory domain;
Phosphorylation;
Cofactor;
Expression
- MeSH:
Dopamine;
Models, Animal;
Neurons;
Parkinson Disease;
Phosphorylation;
Protein Stability;
RNA, Messenger;
Tyrosine 3-Monooxygenase*;
Tyrosine*;
United Nations
- From:Journal of the Korean Neurological Association
2001;19(5):514-519
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: For the treatment of Parkinson's disease, dopamine-producing cells or genes involved in producing dopamine or supporting neurons have been tested to replace conventional chemical therapies. Of these, tyrosine hydroxylase (TH) was the most widely used gene for the therapy. Trials using TH via various vectors yielded behavioral improvements in animal models but the effectiveness did not last long enough. As one of the approaches for solving this problem, the regulation of expression of the protein and mRNA of TH was studied. METHODS: Two approaches for a higher and/or more stable expression of TH were pursued. First, the effect of cofactor tetrahydrobiopterin (BH4) on the expression level of TH and second, the effect of deletion which enables TH protein to escape from protease attack, were examined. RESULTS: Cells producing BH4 showed an approximately 10-fold higher TH expression than cells expressing TH alone. When the in vitro modified TH was expressed in NIH-3T3, mutant THs showed elevated protein (17.5 ~68.6 fold) and mRNA (1.8 ~4.6 fold) expression levels at a steady state. CONCLUSIONS: Results suggest that an addition of BH4 has a more positive effect on mRNA expression levels than protein. However, the deletions seem to have a tremen-dous effect on the translation and/or protein stability, but a small effect on the mRNA level. (J Korean Neurol Assoc 19(5):514~519, 2001)
