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腺苷激酶缺乏症会破坏蛋氨酸循环,导致高蛋氨酸血症、脑病和肝功能异常。

Adenosine kinase deficiency disrupts the methionine cycle and causes hypermethioninemia, encephalopathy, and abnormal liver function.

机构信息

Department of Molecular Medicine and Surgery, Science for Life Laboratory, Karolinska Institutet, Stockholm, Sweden.

出版信息

Am J Hum Genet. 2011 Oct 7;89(4):507-15. doi: 10.1016/j.ajhg.2011.09.004. Epub 2011 Sep 28.

Abstract

Four inborn errors of metabolism (IEMs) are known to cause hypermethioninemia by directly interfering with the methionine cycle. Hypermethioninemia is occasionally discovered incidentally, but it is often disregarded as an unspecific finding, particularly if liver disease is involved. In many individuals the hypermethioninemia resolves without further deterioration, but it can also represent an early sign of a severe, progressive neurodevelopmental disorder. Further investigation of unclear hypermethioninemia is therefore important. We studied two siblings affected by severe developmental delay and liver dysfunction. Biochemical analysis revealed increased plasma levels of methionine, S-adenosylmethionine (AdoMet), and S-adenosylhomocysteine (AdoHcy) but normal or mildly elevated homocysteine (Hcy) levels, indicating a block in the methionine cycle. We excluded S-adenosylhomocysteine hydrolase (SAHH) deficiency, which causes a similar biochemical phenotype, by using genetic and biochemical techniques and hypothesized that there was a functional block in the SAHH enzyme as a result of a recessive mutation in a different gene. Using exome sequencing, we identified a homozygous c.902C>A (p.Ala301Glu) missense mutation in the adenosine kinase gene (ADK), the function of which fits perfectly with this hypothesis. Increased urinary adenosine excretion confirmed ADK deficiency in the siblings. Four additional individuals from two unrelated families with a similar presentation were identified and shown to have a homozygous c.653A>C (p.Asp218Ala) and c.38G>A (p.Gly13Glu) mutation, respectively, in the same gene. All three missense mutations were deleterious, as shown by activity measurements on recombinant enzymes. ADK deficiency is a previously undescribed, severe IEM shedding light on a functional link between the methionine cycle and adenosine metabolism.

摘要

已知有四种先天性代谢错误(IEM)可通过直接干扰蛋氨酸循环导致高蛋氨酸血症。高蛋氨酸血症偶尔会被偶然发现,但由于涉及肝脏疾病,通常被视为非特异性发现而被忽视。在许多人中,高蛋氨酸血症会自行消退而不会进一步恶化,但它也可能代表严重进行性神经发育障碍的早期迹象。因此,对不明原因的高蛋氨酸血症进行进一步调查很重要。我们研究了两名受严重发育迟缓及肝功能障碍影响的兄弟姐妹。生化分析显示血浆中甲硫氨酸、S-腺苷甲硫氨酸(AdoMet)和 S-腺苷同型半胱氨酸(AdoHcy)水平升高,但同型半胱氨酸(Hcy)水平正常或轻度升高,表明蛋氨酸循环受阻。我们排除了 S-腺苷同型半胱氨酸水解酶(SAHH)缺乏症,因为它会导致类似的生化表型,方法是使用遗传和生化技术,并假设由于不同基因中的隐性突变,SAHH 酶存在功能障碍。通过外显子组测序,我们在腺苷激酶基因(ADK)中发现了一个纯合 c.902C>A(p.Ala301Glu)错义突变,该突变的功能与该假设完全吻合。增加的尿腺苷排泄证实了兄弟姐妹的 ADK 缺乏症。在两个具有相似表现的无关家庭中,又发现了另外 4 名个体,分别显示出相同基因中的 c.653A>C(p.Asp218Ala)和 c.38G>A(p.Gly13Glu)突变。所有三个错义突变均为有害突变,这可从重组酶的活性测量中看出。ADK 缺乏症是一种以前未描述的严重 IEM,它阐明了蛋氨酸循环与腺苷代谢之间的功能联系。

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