RARS (gene) explained

Arginyl-tRNA synthetase, cytoplasmic is an enzyme that in humans is encoded by the RARS gene.[1] [2]

Aminoacyl-tRNA synthetases catalyze the aminoacylation of tRNA by their cognate amino acid. Because of their central role in linking amino acids with nucleotide triplets contained in tRNAs, aminoacyl-tRNA synthetases are thought to be among the first proteins that appeared in evolution. Arginyl-tRNA synthetase belongs to the class-I aminoacyl-tRNA synthetase family.[2]

Genetics

Mutations in RARS cause hypomyelination.[3]

Interactions

RARS (gene) has been shown to interact with QARS.[4]

Further reading

Notes and References

  1. Girjes AA, Hobson K, Chen P, Lavin MF . Cloning and characterization of cDNA encoding a human arginyl-tRNA synthetase . Gene . 164 . 2 . 347–50 . October 1995 . 7590355 . 10.1016/0378-1119(95)00502-W .
  2. Web site: Entrez Gene: RARS arginyl-tRNA synthetase.
  3. Wolf NI, Salomons GS, Rodenburg RJ, Pouwels PJ, Schieving JH, Derks TG, Fock JM, Rump P, van Beek DM, van der Knaap MS, Waisfisz Q . Mutations in RARS cause hypomyelination . Annals of Neurology . 76 . 1 . 134–9 . July 2014 . 24777941 . 10.1002/ana.24167 . 27717491 .
  4. Kim T, Park SG, Kim JE, Seol W, Ko YG, Kim S . Catalytic peptide of human glutaminyl-tRNA synthetase is essential for its assembly to the aminoacyl-tRNA synthetase complex . The Journal of Biological Chemistry . 275 . 28 . 21768–72 . July 2000 . 10801842 . 10.1074/jbc.M002404200 . free .