Wans Stefan, Schüttler Katrin, Jakubiczka Sibylle, Müller Andreas, Luley Claus, Dierkes Jutta
Institute of Clinical Chemistry, University Hospital Magdeburg, Magdeburg, Germany.
Clin Chem Lab Med. 2003 Nov;41(11):1532-6. doi: 10.1515/CCLM.2003.235.
A relatively new method for the detection of single nucleotide polymorphisms is the use of denaturing high-performance liquid chromatography (DHPLC). DHPLC was used to analyse the transcobalamin II 776C>G polymorphism in DNA from 159 healthy elderly. Furthermore, cobalamin, folate, homocysteine and holo-transcobalamin II (holo-TC II) were measured. The allele frequency of the G-allele was 17% with n = 55 harbouring the CC genotype, n = 77 being heterozygous and n = 27 showing the GG genotype. Holo-TC II concentrations were significantly decreased in patients harbouring the GG genotype. There was no effect on cobalamin, methylmalonyl-CoA, folate or homocysteine concentrations. A new G>A variant at nucleotide position 810 in the TC II gene was detected by an altered peak pattern in the DHPLC and further elucidated by direct sequencing. The TC II G810A variant is a silent mutation without replacement of the corresponding amino acid (alanine) at position 270 in the TC II protein and was only found as a heterozygous genotype in a single patient. The new variant would have been undetected by other methods used for single nucleotide polymorphism detection, e.g., restriction fragment length polymorphism analysis. The results suggest that the common TC II 776C>G polymorphism has no major influence on vitamin B12 metabolism.
一种相对较新的单核苷酸多态性检测方法是变性高效液相色谱法(DHPLC)。利用DHPLC分析了159名健康老年人DNA中的转钴胺素II 776C>G多态性。此外,还检测了钴胺素、叶酸、同型半胱氨酸和全转钴胺素II(holo-TC II)。G等位基因的频率为17%,其中55人携带CC基因型,77人为杂合子,27人表现为GG基因型。携带GG基因型的患者中holo-TC II浓度显著降低。对钴胺素、甲基丙二酰辅酶A、叶酸或同型半胱氨酸浓度没有影响。通过DHPLC中峰型的改变检测到转钴胺素II基因第810位核苷酸处有一个新的G>A变异,并通过直接测序进一步阐明。转钴胺素II G810A变异是一个沉默突变,在转钴胺素II蛋白的第270位没有替换相应的氨基酸(丙氨酸),仅在一名患者中发现为杂合基因型。其他用于单核苷酸多态性检测的方法,如限制性片段长度多态性分析,无法检测到这个新变异。结果表明,常见的转钴胺素II 776C>G多态性对维生素B12代谢没有重大影响。