Редактирование: MAT1A

S-adenosylmethionine synthase isoform type-1 (EC 2.5.1.6) (AdoMet synthase 1) (Methionine adenosyltransferase 1) (MAT 1) (Methionine adenosyltransferase I/III) (MAT-I/III) [AMS1] [MATA1]

==Publications==

{{medline-entry
|title=Longevity candidate genes and their association with personality traits in the elderly.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/22213687
|abstract=Human longevity and personality traits are both heritable and are consistently linked at the phenotypic level. We test the hypothesis that candidate genes influencing longevity in lower organisms are associated with variance in the five major dimensions of human personality (measured by the NEO-FFI and IPIP inventories) plus related mood states of anxiety and depression. Seventy single nucleotide polymorphisms (SNPs) in six brain expressed, longevity candidate genes (AFG3L2, FRAP1, [[MAT1A]], [[MAT2A]], [[SYNJ1]], and [[SYNJ2]]) were typed in over 1,000 70-year old participants from the Lothian Birth Cohort of 1936 (LBC1936). No SNPs were associated with the personality and psychological distress traits at a Bonferroni corrected level of significance (P < 0.0002), but there was an over-representation of nominally significant (P < 0.05) SNPs in the synaptojanin-2 ([[SYNJ2]]) gene associated with agreeableness and symptoms of depression. Eight SNPs which showed nominally significant association across personality measurement instruments were tested in an extremely large replication sample of 17,106 participants. SNP rs350292, in [[SYNJ2]], was significant: the minor allele was associated with an average decrease in NEO agreeableness scale scores of 0.25 points, and 0.67 points in the restricted analysis of elderly cohorts (most aged >60 years). Because we selected a specific set of longevity genes based on functional genomics findings, further research on other longevity gene candidates is warranted to discover whether they are relevant candidates for personality and psychological distress traits.
|mesh-terms=* Adolescent
* Adult
* Aged
* Aged, 80 and over
* Alleles
* Anxiety Disorders
* Cohort Studies
* Depression
* Female
* Genetic Markers
* Genotype
* Haplotypes
* Humans
* Longevity
* Male
* Middle Aged
* Personality Disorders
* Personality Tests
* Phenotype
* Phosphoric Monoester Hydrolases
* Polymerase Chain Reaction
* Polymorphism, Single Nucleotide
* Young Adult

|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583011
}}
{{medline-entry
|title=Evolutionary conserved longevity genes and human cognitive abilities in elderly cohorts.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/22045296
|abstract=Genetic influences have an important role in the ageing process. The genetic factors that influence success in bodily ageing may also contribute to the successful ageing of cognitive abilities. A comparative genomics approach found longevity genes conserved between yeast Saccharomyces cerevisiae and nematode Caenorhabditis elegans. We hypothesised that these longevity genes influence variance in cognitive ability and age-related cognitive decline in humans. Here, we investigated six of these genes that have human orthologs and show expression in the brain. We tested [[AFG3L2]] (MIM: 604581, AFG3 ATPase family gene 3-like 2 (yeast)), FRAP1 (MIM: 601231, a FK506 binding protein 12-rapamycin associated protein), [[MAT1A]], [[MAT2A]] (MIM: 610550 and 601468, methionine adenosyltransferases I alpha and II alpha, respectively), [[SYNJ1]] and [[SYNJ2]] (MIM: 604297 and 609410, synaptojanin-1 and synaptojanin-2, respectively) in approximately 1000 healthy older Scots: the Lothian Birth Cohort 1936 (LBC1936). They were tested on general cognitive ability at age 11 years. At a mean age of 70 years, they re-sat the same general cognitive ability test and underwent an additional battery of diverse cognitive tests. In all, 70 tag and functional SNPs in the six longevity genes were genotyped and tested for association with cognition and cognitive ageing in LBC1936. Suggestive associations were detected between SNPs in [[SYNJ2]], [[MAT1A]], [[AFG3L2]] and [[SYNJ1]] and a general memory factor and general cognitive ability at age 11 and 70 years. Replication studies for cognitive ability associations were performed in 2506 samples from the Cognitive Ageing Genetics in England and Scotland consortium. A meta-analysis replicated the [[SYNJ2]] association with cognitive abilities (lowest P=0.00077). [[SYNJ2]] is a novel gene in which variation is potentially associated with cognitive abilities.
|mesh-terms=* Adolescent
* Adult
* Aged
* Aged, 80 and over
* Aging
* Child
* Child, Preschool
* Cognition
* Cohort Studies
* Evolution, Molecular
* Female
* Genotype
* Humans
* Longevity
* Male
* Memory
* Middle Aged
* Nerve Tissue Proteins
* Phosphoric Monoester Hydrolases
* Polymorphism, Single Nucleotide
* Reproducibility of Results

|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3283186
}}