Histidine–tRNA ligase, cytoplasmic

HARS1
Identifiers
AliasesHARS1, HRS, USH3B, CMT2W, histidyl-tRNA synthetase, HARS, histidyl-tRNA synthetase 1
External IDsOMIM: 142810; MGI: 108087; GeneCards: HARS1
Available structures
PDBOrtholog search: PDBe RCSB
Enzyme activity
EC #BRENDAExPASyKEGGMetaCyc
6.1.1.21↗↗↗↗
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_008214

RefSeq (protein)

NP_032240

Location (UCSC)Chr 5: 140.67 – 140.69 MbChr 18: 36.9 – 36.92 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Histidine–tRNA ligase, cytoplasmic, also called histidyl-tRNA synthetase 1, is an enzyme which in humans is encoded by the HARS1 gene (previously HARS). As a histidine–tRNA ligase, this enzyme functions to attach the amino acid histidine to its corresponding (cognate) transfer RNA (tRNAHis), which is required for RNA-to-protein translation.

Function

Aminoacyl-tRNA synthetases are a class of enzymes that charge tRNAs with their cognate amino acids. The protein encoded by this gene is a cytoplasmic enzyme which belongs to the class II family of aminoacyl tRNA synthetases. The enzyme is responsible for the synthesis of histidyl-transfer RNA, which is essential for the incorporation of histidine into proteins. The gene is located in a head-to-head orientation with HARS2 on chromosome five, where the homologous genes share a bidirectional promoter.

Clinical significance

The gene product is a frequent target of autoantibodies in the human autoimmune disease polymyositis/dermatomyositis. Pathogenic mutations in HARS1 are the cause of Type IIIB usher syndrome (USH3B), which is associated with progressive hearing and vision loss.

Interactions

HARS has been shown to interact with EEF1B2 and EEF1G.

See also

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000170445 – Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000001380 – Ensembl, 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. 1 2 3 "Entrez Gene: HARS histidyl-tRNA synthetase".
  6. ↑ Wasmuth JJ, Carlock LR (1986). "Chromosomal localization of human gene for histidyl-tRNA synthetase: clustering of genes encoding aminoacyl-tRNA synthetases on human chromosome 5". Somat. Cell Mol. Genet. 12 (5): 513–7. doi:10.1007/BF01539922. PMID 3464104. S2CID 28520231.
  7. 1 2 Freist W, Verhey JF, Rühlmann A, Gauss DH, Arnez JG (1999). "Histidyl-tRNA synthetase". Biol. Chem. 380 (6): 623–46. doi:10.1515/BC.1999.079. PMID 10430027.
  8. ↑ "USHER SYNDROME, TYPE IIIB; USH3B". Online Mendelian Inheritance in Man. Johns Hopkins University. Retrieved 2026-09-27.
  9. 1 2 Sang Lee J, Gyu Park S, Park H, Seol W, Lee S, Kim S (2002). "Interaction network of human aminoacyl-tRNA synthetases and subunits of elongation factor 1 complex". Biochem. Biophys. Res. Commun. 291 (1): 158–64. doi:10.1006/bbrc.2002.6398. PMID 11829477.

Further reading