Hereditary tyrosinemia type 1 metabolites impair DNA excision repair pathways.
E van Dyk, A Steenkamp, G Koekemoer, P J Pretorius
Index: Biochem. Biophys. Res. Commun. 401(1) , 32-6, (2010)
Full Text: HTML
Abstract
Hereditary tyrosinemia type 1 is an autosomal recessive metabolic disorder, which is caused by a defective fumarylacetoacetate hydrolase enzyme, and consequently metabolites such as succinylacetone and p-hydroxyphenylpyruvate accumulate. We used a modified comet assay to determine the effect of these metabolites on base- and nucleotide excision repair pathways. Our results indicate that the metabolites affected the repair mechanisms differently, since the metabolites had a bigger detrimental effect on BER than on NER.Copyright © 2010 Elsevier Inc. All rights reserved.
Related Compounds
Related Articles:
2007-08-17
[J. Biol. Chem. 282 , 23841-53, (2007)]
2014-08-05
[Biochemistry 53(30) , 5034-41, (2014)]
2011-01-01
[Bioorg. Med. Chem. 19 , 3320-40, (2011)]
2010-06-22
[Proc. Natl. Acad. Sci. U. S. A. 107(25) , 11313-8, (2010)]
2010-04-01
[J. Biosci. Bioeng. 109(4) , 369-71, (2010)]