Prieto-Alamo M J, Laval F
Unité 347 Institut National de la Santé et de la Recherche Médicale, 80 Rue du Général Leclerc, 94276 Le Kremlin Bicêtre, France.
Proc Natl Acad Sci U S A. 1998 Oct 13;95(21):12614-8. doi: 10.1073/pnas.95.21.12614.
Hereditary tyrosinemia type I (HT1) is an autosomal recessive inborn error of metabolism caused by the deficiency of fumarylacetoacetate hydrolase, the last enzyme in the tyrosine catabolism pathway. This defect results in accumulation of succinylacetone (SA) that reacts with amino acids and proteins to form stable adducts via Schiff base formation, lysine being the most reactive amino acid. HT1 patients surviving beyond infancy are at considerable risk for the development of hepatocellular carcinoma, and a high level of chromosomal breakage is observed in HT1 cells, suggesting a defect in the processing of DNA. In this paper we show that the overall DNA-ligase activity is low in HT1 cells (about 20% of the normal value) and that Okazaki fragments are rejoined at a reduced rate compared with normal fibroblasts. No mutation was found by sequencing the ligase I cDNA from HT1 cells, and the level of expression of the ligase I mRNA was similar in normal and HT1 fibroblasts, suggesting the presence of a ligase inhibitor. SA was shown to inhibit in vitro the overall DNA-ligase activity present in normal cell extracts. The activity of purified T4 DNA-ligase, whose active site is also a lysine residue, was inhibited by SA in a dose-dependent manner. These results suggest that accumulation of SA reduces the overall ligase activity in HT1 cells and indicate that metabolism errors may play a role in regulating enzymatic activities involved in DNA replication and repair.
I型遗传性酪氨酸血症(HT1)是一种常染色体隐性遗传的先天性代谢紊乱疾病,由酪氨酸分解代谢途径中的最后一种酶——富马酰乙酰乙酸水解酶缺乏所致。这种缺陷导致琥珀酰丙酮(SA)蓄积,SA通过席夫碱形成与氨基酸和蛋白质反应形成稳定加合物,其中赖氨酸是最具反应性的氨基酸。存活至婴儿期后的HT1患者患肝细胞癌的风险相当高,并且在HT1细胞中观察到高水平的染色体断裂,提示DNA加工存在缺陷。在本文中,我们表明HT1细胞中的总体DNA连接酶活性较低(约为正常值的20%),与正常成纤维细胞相比,冈崎片段的重新连接速率降低。对HT1细胞的连接酶I cDNA进行测序未发现突变,正常成纤维细胞和HT1成纤维细胞中连接酶I mRNA的表达水平相似,提示存在连接酶抑制剂。SA在体外可抑制正常细胞提取物中的总体DNA连接酶活性。纯化的T4 DNA连接酶的活性位点也是一个赖氨酸残基,其活性受到SA的剂量依赖性抑制。这些结果表明,SA的蓄积降低了HT1细胞中的总体连接酶活性,并表明代谢错误可能在调节参与DNA复制和修复的酶活性中起作用。