Wood Thomas C, Salavagionne Oreste E, Mukherjee Baidehi, Wang Liewei, Klumpp Annette F, Thomae Bianca A, Eckloff Bruce W, Schaid Daniel J, Wieben Eric D, Weinshilboum Richard M
Division of Clinical Pharmacology, Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, MN 55905, USA.
J Biol Chem. 2006 Mar 17;281(11):7364-73. doi: 10.1074/jbc.M512227200. Epub 2006 Jan 6.
Arsenic contaminates ground water worldwide. Methylation is an important reaction in the biotransformation of arsenic. We set out to study the pharmacogenetics of human arsenic methyltransferase (AS3MT, previously CYT19). After cloning the human AS3MT cDNA, we annotated the human gene and resequenced its 5'-flanking region, exons, and splice junctions using 60 DNA samples from African-American (AA) and 60 samples from Caucasian-American (CA) subjects. We observed 26 single nucleotide polymorphisms (SNPs), including 3 non-synonymous cSNPs, as well as a variable number of tandem repeats in exon 1 within an area encoding the cDNA 5'-untranslated region. The nonsynonymous cSNPs included T860C (M287T) with frequencies of 10.8 and 10% in AA and CA subjects, respectively, as well as C517T (A173W) in one AA and C917T (T306I) in one CA sample. Haplotype analysis showed that Ile(306) was linked to Thr(287), so this double variant allozyme was also studied functionally. After expression in COS-1 cells and correction for transfection efficiency, the Trp(173) allozyme displayed 31%, Thr(287) 350%, Ile(306) 4.8%, and Thr(287)/Ile(306) 6.2% of the activity of the wild type (WT) allozyme, with 20, 190, 4.4, and 7.9% of the level of WT immunoreactive protein, respectively. Apparent K(m) values for S-adenosyl-l-methionine were 4.6, 3.1, and 11 mum for WT, Trp(173), and Thr(287) allozymes, with K(m) values for sodium arsenite with the same allozymes of 11.8, 8.9, and 4.5mum. The Ile(306) and Thr(287)/Ile(306) allozymes expressed too little activity for inclusion in the substrate kinetic studies. Expression of reporter gene constructs for the 5'-flanking region and the variable number of tandem repeats in the 5'-untranslated region demonstrated cell line-dependent variation in reporter gene expression, with shorter repeats associated with increased transcription in HepG2 cells. These results raise the possibility that inherited variation in AS3MT may contribute to variation in arsenic metabolism and, perhaps, arsenic-dependent carcinogenesis in humans.
砷污染着全球的地下水。甲基化是砷生物转化过程中的一个重要反应。我们着手研究人类砷甲基转移酶(AS3MT,之前称为CYT19)的药物遗传学。克隆人类AS3MT cDNA后,我们对该人类基因进行注释,并使用60份非裔美国人(AA)的DNA样本和60份美籍高加索人(CA)的样本对其5'侧翼区域、外显子和剪接连接进行重测序。我们观察到26个单核苷酸多态性(SNP),包括3个非同义cSNP以及在编码cDNA 5'非翻译区的区域内第1外显子中的可变数目串联重复序列。非同义cSNP包括T860C(M287T),在AA和CA受试者中的频率分别为10.8%和10%,以及在1个AA样本中的C517T(A173W)和在1个CA样本中的C917T(T306I)。单倍型分析表明Ile(306)与Thr(287)连锁,因此也对这种双变体同工酶进行了功能研究。在COS-1细胞中表达并校正转染效率后,Trp(173)同工酶的活性为野生型(WT)同工酶的31%,Thr(287)为350%,Ile(306)为4.8%,Thr(287)/Ile(306)为6.2%,其WT免疫反应性蛋白水平分别为WT的20%、190%、4.4%和7.9%。S-腺苷-L-甲硫氨酸的表观K(m)值对于WT、Trp(173)和Thr(287)同工酶分别为4.6、3.1和11μM,亚砷酸钠的K(m)值对于相同同工酶分别为11.8、8.9和4.5μM。Ile(306)和Thr(287)/Ile(306)同工酶表达的活性过低,无法纳入底物动力学研究。5'侧翼区域和5'非翻译区可变数目串联重复序列的报告基因构建体的表达显示出报告基因表达的细胞系依赖性变化,较短的重复序列与HepG2细胞中转录增加相关。这些结果增加了一种可能性,即AS3MT的遗传变异可能导致人类砷代谢的变异,或许还会导致砷依赖性致癌作用。