Thomas David J, Li Jiaxin, Waters Stephen B, Xing Weibing, Adair Blakely M, Drobna Zuzana, Devesa Vicenta, Styblo Miroslav
Pharmacokinetics Branch, Experimental Toxicology Division, National Health and Environmental Effects Research Laboratory, Office of Research and Development, US Environmental Protection Agency, Research Triangle Park, NC 27711, USA.
Exp Biol Med (Maywood). 2007 Jan;232(1):3-13.
Metabolic conversion of inorganic arsenic into methylated products is a multistep process that yields mono-, di-, and trimethylated arsenicals. In recent years, it has become apparent that formation of methylated metabolites of inorganic arsenic is not necessarily a detoxification process. Intermediates and products formed in this pathway may be more reactive and toxic than inorganic arsenic. Like all metabolic pathways, understanding the pathway for arsenic methylation involves identification of each individual step in the process and the characterization of the molecules which participate in each step. Among several arsenic methyltransferases that have been identified, arsenic (+3 oxidation state) methyltransferase is the one best characterized at the genetic and functional levels. This review focuses on phylogenetic relationships in the deuterostomal lineage for this enzyme and on the relation between genotype for arsenic (+3 oxidation state) methyltransferase and phenotype for conversion of inorganic arsenic to methylated metabolites. Two conceptual models for function of arsenic (+3 oxidation state) methyltransferase which posit different roles for cellular reductants in the conversion of inorganic arsenic to methylated metabolites are compared. Although each model accurately represents some aspects of enzyme's role in the pathway for arsenic methylation, neither model is a fully satisfactory representation of all the steps in this metabolic pathway. Additional information on the structure and function of the enzyme will be needed to develop a more comprehensive model for this pathway.
无机砷代谢转化为甲基化产物是一个多步骤过程,会产生一甲基、二甲基和三甲基砷化物。近年来,无机砷甲基化代谢产物的形成不一定是解毒过程这一点已变得很明显。该途径中形成的中间体和产物可能比无机砷更具反应性和毒性。与所有代谢途径一样,了解砷甲基化途径涉及识别该过程中的每个单独步骤以及参与每个步骤的分子的特征。在已鉴定的几种砷甲基转移酶中,砷(+3氧化态)甲基转移酶是在遗传和功能水平上表征得最好的一种。本综述重点关注该酶在口后动物谱系中的系统发育关系,以及砷(+3氧化态)甲基转移酶的基因型与无机砷转化为甲基化代谢产物的表型之间的关系。比较了两种关于砷(+3氧化态)甲基转移酶功能的概念模型,这两种模型对细胞还原剂在无机砷转化为甲基化代谢产物过程中的作用提出了不同的假设。尽管每个模型都准确地反映了该酶在砷甲基化途径中的某些作用,但没有一个模型能完全令人满意地代表该代谢途径中的所有步骤。需要有关该酶结构和功能的更多信息来开发一个更全面的该途径模型。