Cell Senescence Entries for TYMS
- Cell Types
- Melanoma
- Cell Lines
- SK-MEL-19, SK-MEL-29
- Cancer Cell?
- Yes
- Method
- Overexpression
- Type of senescence
- Oncogene-induced
- Senescence Effect
- Inhibits
- Primary Reference
- Mannava et al. (2013) Ribonucleotide reductase and thymidylate synthase or exogenous deoxyribonucleosides reduce DNA damage and senescence caused by C-MYC depletion. Aging (Albany NY) 4(12)917-22 (PubMed)
TYMS Gene Information
- HGNC symbol
- TYMS
- Aliases
- HsT422; TMS; TS; Tsase
- Common name
- thymidylate synthetase
- Entrez Id
- 7298
- Description
- Thymidylate synthase catalyzes the methylation of deoxyuridylate to deoxythymidylate using, 10-methylenetetrahydrofolate (methylene-THF) as a cofactor. This function maintains the dTMP (thymidine-5-prime monophosphate) pool critical for DNA replication and repair. The enzyme has been of interest as a target for cancer chemotherapeutic agents. It is considered to be the primary site of action for 5-fluorouracil, 5-fluoro-2-prime-deoxyuridine, and some folate analogs. Expression of this gene and that of a naturally occurring antisense transcript, mitochondrial enolase superfamily member 1 (GeneID:55556), vary inversely when cell-growth progresses from late-log to plateau phase. Polymorphisms in this gene may be associated with etiology of neoplasia, including breast cancer, and response to chemotherapy. [provided by RefSeq, Aug 2017].
TYMS Ontologies
- Gene Ontology
-
Process: GO:71897; DNA biosynthetic process
GO:32259; methylation
GO:9165; nucleotide biosynthetic process
GO:46683; response to organophosphorus
GO:17148; negative regulation of translation
GO:6206; pyrimidine nucleobase metabolic process
GO:6231; dTMP biosynthetic process
GO:6235; dTTP biosynthetic process
GO:6417; regulation of translation
GO:7568; aging
GO:7623; circadian rhythm
GO:9410; response to xenobiotic stimulus
GO:9636; response to toxic substance
GO:14070; response to organic cyclic compound
GO:19860; uracil metabolic process
GO:32570; response to progesterone
GO:33189; response to vitamin A
GO:34097; response to cytokine
GO:35999; tetrahydrofolate interconversion
GO:45471; response to ethanol
GO:46653; tetrahydrofolate metabolic process
GO:48589; developmental growth
GO:51216; cartilage development
GO:51384; response to glucocorticoid
GO:51593; response to folic acid
GO:60574; intestinal epithelial cell maturation
GO:97421; liver regeneration
Cellular component: GO:5634; nucleus
GO:5737; cytoplasm
GO:16020; membrane
GO:5739; mitochondrion
GO:5743; mitochondrial inner membrane
GO:5759; mitochondrial matrix
GO:5829; cytosol
GO:5730; nucleolus
Function: GO:16740; transferase activity
GO:8168; methyltransferase activity
GO:3824; catalytic activity
GO:900; translation repressor activity, mRNA regulatory element binding
GO:5542; folic acid binding
GO:1990825; sequence-specific mRNA binding
GO:3729; mRNA binding
GO:4799; thymidylate synthase activity
GO:16741; transferase activity, transferring one-carbon groups
GO:42803; protein homodimerization activity
GO:1901363; heterocyclic compound binding
Homologs of TYMS in Model Organisms
- Caenorhabditis elegans
- CELE_Y110A7A.4
- Danio rerio
- tyms
- Drosophila melanogaster
- Ts
- Mus musculus
- Tyms
- Rattus norvegicus
- Tyms
- Saccharomyces cerevisiae
- CDC21
In other databases
- CellAge gene expression
- This gene is present as TYMS
External links
- OMIM
- 188350
- Ensembl
- ENSG00000176890
- Entrez Gene
- 7298
- UniGene
- 369762
- 1000 Genomes
- 1000 Genomes
- HPRD
- GenAtlas
- TYMS
- GeneCards
- TYMS