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首页> 外文期刊>Analytical and Bioanalytical Chemistry >Direct molecular haplotyping of multiple polymorphisms within exon 4 of the human catechol-O-methyltransferase gene by liquid chromatography–electrospray ionization time-of-flight mass spectrometry
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Direct molecular haplotyping of multiple polymorphisms within exon 4 of the human catechol-O-methyltransferase gene by liquid chromatography–electrospray ionization time-of-flight mass spectrometry

机译:液相色谱-电喷雾电离飞行时间质谱法直接检测人儿茶酚-O-甲基转移酶基因第4外显子内多个多态性的分子单倍型

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摘要

The applicability of ion-pair reversed-phase high-performance liquid chromatography hyphenated to electrospray ionization time-of-flight mass spectrometry (ICEMS) for the haplotyping of five SNPs (rs769223, rs4818, rs4986871, rs8192488, rs4680) located within exon 4 of the human catechol-O-methyltransferase (COMT, EC 2.1.1.6) gene is demonstrated. Two differently sized products of polymerase chain reaction—a 71-bp amplicon partially covering the sequence of a 124-bp amplicon—were used to determine unequivocally the allelic states of the single nucleotide polymorphisms linked on both chromosomes. The two amplicons were co-loaded onto the chromatographic column and simultaneously analyzed within a single gradient run. Using the described strategy, 101 individuals representing an Austrian population sample were typed. The obtained haplotype frequencies will serve as reference values in future association studies to examine the impact of the COMT gene on neuropsychiatric disorders. Additionally, two newly discovered polymorphic sites within the sequence of the COMT gene are described (a synonymous C>T mutation at the third position of the amino acid codon 99 in the soluble COMT protein or 149 in the membrane-bound COMT protein; a non-synonymous G>A substitution at the second position of the amino acid codon 95 in the soluble COMT protein or 145 in the membrane-bound-COMT protein).
机译:离子对反相高效液相色谱联用电喷雾电离飞行时间质谱(ICEMS)进行单倍型位于5号外显子4中的5个SNP(rs769223,rs4818,rs4986871,rs8192488,rs4680)的适用性证明了人儿茶酚-O-甲基转移酶(COMT,EC 2.1.1.6)基因。两种不同大小的聚合酶链反应产物(一个71 bp的扩增子部分覆盖了124 bp的扩增子序列)被用来确定两个染色体上连接的单核苷酸多态性的等位基因状态。将两个扩增子共上样到色谱柱上,并在一个梯度运行中同时进行分析。使用描述的策略,输入代表奥地利人口样本的101个人。获得的单倍型频率将在将来的关联研究中用作参考值,以检查COMT基因对神经精神疾病的影响。另外,还描述了COMT基因序列中的两个新发现的多态性位点(同义C> T突变位于可溶性COMT蛋白中第99个氨基酸密码子的第三位或膜结合COMT蛋白中第149位;非-在可溶性COMT蛋白中的氨基酸密码子95的第二个位置或膜结合的COMT蛋白中的145位的第二个同义G> A取代)。

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