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DNA methylation status is not impaired in treated cystathionine beta-synthase (CBS) deficient patients

被引：16
作者：
Heil, Sandra G.
Riksen, Niels P.
Boers, Godfried H.
Smulders, Yvo
Blom, Henk J.
机构：
[1] Radboud Univ Nijmegen, Nijmegen Med Ctr, Lab Pediat & Neurol, NL-6500 HB Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Nijmegen Med Ctr, Dept Pharmacol & Toxicol, NL-6500 HB Nijmegen, Netherlands
[3] Radboud Univ Nijmegen, Nijmegen Med Ctr, Dept Internal Med, NL-6500 HB Nijmegen, Netherlands
[4] Vrije Univ Amsterdam, Ctr Med, Amsterdam, Netherlands
来源：
MOLECULAR GENETICS AND METABOLISM | 2007年 / 91卷 / 01期
关键词：
homocysteine; CBS; H19; methylation;
D O I：
10.1016/j.ymgme.2007.01.008
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
Background: Cystathionine beta-synthase (CBS) deficiency is an inborn error of metabolism that is biochemically characterized by severe hyperhomocysteinemia and homocystinuria. In tissues of mice deficient for CBS it has been demonstrated that global DNA methylation and DNA methylation of the H19 differentially methylated region (DMR) were impaired. In this study we aimed to investigate whether DNA methylation is disturbed in patients with hyperhotnocysteinemia due to CBS-deficiency. Methods: Genomic DNA was isolated from heparin blood from nine CBS deficient patients that were treated with homomcysteine-lowering therapy and eight healthy controls. Global DNA -methylation was measured by liquid chromatography-electrospay ionization-tandem mass spectrometry and gene-specific DNA methylation of the H19 DMR was determined by bisulphite-sequencing. Results: Homocysteine, AdoMet and AdoHcy levels were significantly elevated, whereas no differences in AdoMet:AdoHcy ratio were observed in plasma of treated CBS deficient patients compared with controls. Global DNA methylation and gene-specific DNA methylation of the H19 DMR was not different between CBS deficient patients and controls. Conclusion: We demonstrate that DNA methylation is not impaired in treated CBS deficient patients. Further studies are necessary to investigate the precise role of homocysteine-lowering therapy in relation to DNA methylation in patients with homocystinuria. 2007 Elsevier Inc. All rights reserved.
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页码：55 / 60
页数：6
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