MTHFD2L
NAD-dependent methylenetetrahydrofolate dehydrogenase 2-like protein (MTHFD2L), also known as bifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase 2, is an enzyme that in humans is encoded by the MTHFD2L gene on chromosome 4.[5][6] This enzyme localizes to the inner mitochondrial membrane, where it performs the NADP+-dependent dehydrogenase/cyclohydrolase activity as part of the mitochondrial pathway to convert folate to formate.[7] It is associated with fluctuations in cytokine secretion in response to viral infections and vaccines.[8]
Structure
[edit]The MTHFD2L gene consists of nine exons and is conserved among mammals. This gene encodes a 340-residue protein that is homologous to the mitochondrial bifunctional dehydrogenase/cyclohydrolase (MTHFD2) and to the N-terminal dehydrogenase/cyclohydrolase domains of cytoplasmic and mitochondrial C1-THF syntheses (MTHFD1 and MTHFD1L, respectively). The MTHFD2L protein contains a predicted N-terminal mitochondrial targeting sequence and four amino acids (Lys-93, Arg-206, Gly-211, and Arg-238) necessary for the protein's dehydrogenase/cyclohydrolase activity. Three classes of MTHFD2L RNA transcripts have been detected at equal levels in adult human brain and placenta, though their translation into stable proteins in vivo has not been confirmed.[7]
Function
[edit]MTHFD2L is a member of the tetrahydrofolate dehydrogenase/cyclohydrolase family.[6] This enzyme is expressed in all adult tissues and localizes to the mitochondria, specifically as a peripheral membrane protein in the mitochondrial matrix side of the inner mitochondrial membrane. Within the mitochondria, it participates the conversion of folate to formate as part of the mitochondrial pathway for 1-carbon metabolism.[7][8] In the final step of this pathway, the NADP+-dependent CH2-THF dehydrogenase/CH+-THF cyclohydrolase activity of bifunctional MTHFD2L complements the 10-CHO-THF synthetase activity of monofunctional MTHFD1L.[7][9] The formate produced via the mitochondrial pathway can contribute to purine and thymidine synthesis and homocysteine remethylation into methionine, as well as be converted into 1-carbon units to fuel the cytoplasmic pathway of folate metabolism.[9]
Clinical significance
[edit]In a GWAS study concerning variations in cytokine responses observed in smallpox vaccine recipients, a number of SNPs associated with variations in IL-1β secretion were identified in or within the vicinity of the MTHFD2L gene. Identification of the genetic elements controlling cytokine secretion in response to viral infection or vaccination can improve next-generation vaccines to provide robust immune protection while avoiding adverse effects.[8]
See also
[edit]References
[edit]- ^ a b c GRCh38: Ensembl release 89: ENSG00000163738 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000029376 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Entrez Gene: MTHFD2L methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2-like".
- ^ a b "UniProtKB: Q9H903 (MTD2L_HUMAN)".
- ^ a b c d Bolusani S, Young BA, Cole NA, Tibbetts AS, Momb J, Bryant JD, Solmonson A, Appling DR (Feb 2011). "Mammalian MTHFD2L encodes a mitochondrial methylenetetrahydrofolate dehydrogenase isozyme expressed in adult tissues". The Journal of Biological Chemistry. 286 (7): 5166–74. doi:10.1074/jbc.M110.196840. PMC 3037629. PMID 21163947.
- ^ a b c Kennedy RB, Ovsyannikova IG, Pankratz VS, Haralambieva IH, Vierkant RA, Poland GA (Sep 2012). "Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients". Human Genetics. 131 (9): 1403–21. doi:10.1007/s00439-012-1174-2. PMC 4170585. PMID 22610502.
- ^ a b Watkins D, Rosenblatt DS (Jul 2012). "Update and new concepts in vitamin responsive disorders of folate transport and metabolism". Journal of Inherited Metabolic Disease. 35 (4): 665–70. doi:10.1007/s10545-011-9418-1. PMID 22108709. S2CID 1258801.