Genomic organization of the rat aspartyl-tRNA synthetase gene family: A single active gene and several retropseudogenes

Myriam Lazard, Fabrice Agou, Jean Cavarelli, Marie Thérèse Latreille, Dino Moras, Marc Mirande

Research output: Contribution to journalArticlepeer-review

Abstract

The genomic organization of the gene encoding rat aspartyl-tRNA synthetase (AspRS), a class II aminoacyl-tRNA synthetase (aaRS), was determined. A single active gene and several pseudogenes were isolated from a rat genomic DNA library and characterized. The active DRS1 gene encoding the rat AspRS spans approximately 60 kb and is divided into 16 exons. Exons 8-16, encoding the nt-binding domain of the synthetase, are clustered in the 3'-region of the gene, whereas exons 3, 4, and 5, encoding the anticodon-binding domain are separated by large introns (up to 15 kb) containing LINE sequences. One of the pseudogenes, ΨDRS1, has a nt sequence 93% identical to that of the complete cDNA sequence of rat AspRS but several stop codons interrupt the coding sequence, thus identifying ΨDRS1 to an inactive processed pseudogene. Two repetitive elements from the LINE family are inserted into ΨDRS1. Calculation of nt substitution rates suggests that ΨDRS1 sequences arose approximately 27 Myr ago. The other pseudogene, ΨDRS2, should be more ancient. Taken together, these results clearly demonstrate that the AspRS gene family is composed of only one active gene. The availability of the gene structure of AspRS could help to clarify molecular evolution of class II aaRS.

Original languageEnglish
Pages (from-to)197-205
Number of pages9
JournalGene
Volume180
Issue number1-2
DOIs
Publication statusPublished - 21 Nov 1996

Keywords

  • Aminoacyl-trna synthetase complex
  • Gene structure
  • Line
  • Mammals
  • Pseudogene
  • Retrotransposition

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