Редактирование: AS3MT

Arsenite methyltransferase (EC 2.1.1.137) (Methylarsonite methyltransferase) (S-adenosyl-L-methionine:arsenic(III) methyltransferase) [CYT19]

==Publications==

{{medline-entry
|title=Genetic polymorphisms in [[AS3MT]] and arsenic metabolism in residents of the Red River Delta, Vietnam.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/19371612
|abstract=To elucidate the role of genetic factors in arsenic (As) metabolism, we studied associations of single nucleotide polymorphisms (SNPs) in As ( 3 oxidation state) methyltransferase ([[AS3MT]]) with the As concentrations in hair and urine, and urinary As profile in residents in the Red River Delta, Vietnam. Concentrations of total As in groundwater were 0.7-502 mug/l. Total As levels in groundwater drastically decreased by using sand filter, indicating that the filter could be effective to remove As from raw groundwater. Concentrations of inorganic As (IAs) in urine and total As in hair of males were higher than those of females. A significant positive correlation between monomethylarsonic acid (MMA)/IAs and age in females indicates that older females have higher methylation capacity from IAs to MMA. Body mass index negatively correlated with urinary As concentrations in males. Homozygote for SNPs 4602AA, 35991GG, and 37853GG, which showed strong linkage disequilibrium (LD), had higher percentage (%) of dimethylarsinic acid (DMA) in urine. SNPs 4740 and 12590 had strong LD and associated with urinary %DMA. Although SNPs 6144, 12390, 14215, and 35587 comprised LD cluster, homozygotes in SNPs 12390GG and 35587CC had lower DMA/MMA in urine, suggesting low methylation capacity from MMA to DMA in homo types for these SNPs. SNPs 5913 and 8973 correlated with %MMA and %DMA, respectively. Heterozygote for SNP 14458TC had higher MMA/IAs in urine than TT homozygote, indicating that the heterozygote may have stronger methylation ability of IAs. To our knowledge, this is the first study on the association of genetic factors with As metabolism in Vietnamese.
|mesh-terms=* Adolescent
* Adult
* Aged
* Aging
* Arsenic
* Child
* Female
* Filtration
* Gene Expression Regulation
* Hair
* Humans
* Male
* Methyltransferases
* Middle Aged
* Polymorphism, Single Nucleotide
* Rivers
* Sex Characteristics
* Silicon Dioxide
* Vietnam
* Water Pollutants, Chemical
* Water Supply
* Young Adult

|full-text-url=https://sci-hub.do/10.1016/j.taap.2009.01.015
}}
{{medline-entry
|title=Developmental and genetic modulation of arsenic biotransformation: a gene by environment interaction?
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/17306849
|abstract=The complexity of arsenic toxicology has confounded the identification of specific pathways of disease causation. One focal point of arsenic research is aimed at fully characterizing arsenic biotransformation in humans, a process that appears to be quite variable, producing a mixture of several arsenic species with greatly differing toxic potencies. In an effort to characterize genetic determinants of variability in arsenic biotransformation, a genetic association study of 135 subjects in western Sonora, Mexico was performed by testing 23 polymorphic sites in three arsenic biotransformation candidate genes. One gene, arsenic 3 methyltransferase ([[AS3MT]]), was strongly associated with the ratio of urinary dimethylarsinic acid to monomethylarsonic acid (D/M) in children (7-11 years) but not in adults (18-79 years). Subsequent analyses revealed that the high D/M values associated with variant [[AS3MT]] alleles were primarily due to lower levels of monomethylarsonic acid as percent of total urinary arsenic (%MMA5). In light of several reports of arsenic-induced disease being associated with relatively high %MMA5 levels, these findings raise the possibility that variant [[AS3MT]] individuals may suffer less risk from arsenic exposure than non-variant individuals. These analyses also provide evidence that, in this population, regardless of [[AS3MT]] variant status, children tend to have lower %MMA5 values than adults, suggesting that the global developmental regulation of arsenic biotransformation may interact with genetic variants in metabolic genes to result in novel genetic effects such as those in this report.
|mesh-terms=* Adolescent
* Adult
* Aged
* Aging
* Alleles
* Arsenic
* Arsenicals
* Biotransformation
* Child
* Environmental Exposure
* Female
* Glutathione Transferase
* Humans
* Isoenzymes
* Male
* Methyltransferases
* Middle Aged
* Phenotype
* Polymorphism, Genetic
* Pregnancy
* RNA
* Reverse Transcriptase Polymerase Chain Reaction

|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2040165
}}