Acyl-coA acyltransferase-related enzyme 2 required for viability is a protein that in humans is encoded by the ARV1 gene. It is involved in lipid trafficking. ARV1 is ubiquitously expressed in higher eukaryotes, and in Saccharomyces cerevisiae yeast, is required for viability. Arv1-/- knockout mice display a phenotype with reduced white adipose and favorable blood lipid profiles on a chow diet.[5] ARV1 is hypothesized to be involved in neurodevelopment, as a splice variant of ARV1 with a 40 amino acid truncation causes epileptic encephalopathy in infants.d[6] Arv1-/- mice corroborate this observation.[6] In yeast knockouts, supplanting human ARV1 through plasmid transfection rescues cells from death.[7]

ARV1
Identifiers
AliasesARV1, ARV1 homolog (S. cerevisiae), ARV1 homolog, fatty acid homeostasis modulator, EIEE38, DEE38
External IDsOMIM: 611647; MGI: 1916115; HomoloGene: 41498; GeneCards: ARV1; OMA:ARV1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_022786
NM_001346992

NM_026855
NM_001368372

RefSeq (protein)

NP_001333921
NP_073623

NP_081131
NP_001355301

Location (UCSC)Chr 1: 230.98 – 231 MbChr 8: 125.45 – 125.46 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000173409Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000031982Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Lagor WR, Tong F, Jarrett KE, Lin W, Conlon DM, Smith M, Wang MY, Yenilmez BO, McCoy MG, Fields DW, O'Neill SM, Gupta R, Kumaravel A, Redon V, Ahima RS, Sturley SL, Billheimer JT, Rader DJ (October 2015). "Deletion of murine Arv1 results in a lean phenotype with increased energy expenditure". Nutrition & Diabetes. 5 (10): e181. doi:10.1038/nutd.2015.32. PMC 4631934. PMID 26479315.
  6. ^ a b Palmer EE, Jarrett KE, Sachdev RK, Al Zahrani F, Hashem MO, Ibrahim N, Sampaio H, Kandula T, Macintosh R, Gupta R, Conlon DM, Billheimer JT, Rader DJ, Funato K, Walkey CJ, Lee CS, Loo C, Brammah S, Elakis G, Zhu Y, Buckley M, Kirk EP, Bye A, Alkuraya FS, Roscioli T, Lagor WR (July 2016). "Neuronal deficiency of ARV1 causes an autosomal recessive epileptic encephalopathy". Human Molecular Genetics. 25 (14): 3042–3054. doi:10.1093/hmg/ddw157. PMC 5181598. PMID 27270415.
  7. ^ Swain E, Stukey J, McDonough V, Germann M, Liu Y, Sturley SL, Nickels JT (September 2002). "Yeast cells lacking the ARV1 gene harbor defects in sphingolipid metabolism. Complementation by human ARV1". The Journal of Biological Chemistry. 277 (39): 36152–60. doi:10.1074/jbc.m206624200. PMID 12145310.

Further reading

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