Skip to main content
Log in

A non-LTR retrotransposon from the Hawaiian Drosophila: the LOA element

  • Research Articles
  • Published:
Genetica Aims and scope Submit manuscript

Abstract

An interspersed sequence has been isolated from the genome of D. silvestris, a species endemic to the Hawaiian Islands. The LOA element is 7.7 kb long and its 3′ end consists of (TAA)n tandem repeats. Five different LOA elements were isolated, of which three were truncated at their 5′ ends. Large deletions within the elements were frequent. A consensus sequence of the LOA element has been constructed using the nucleotide sequence of three elements. Two overlapping open reading frames (ORF) are present in the LOA element. In ORF1 two ‘cys’ motifs characteristic for gag proteins are found. The protein translated from ORF2 has similarities with retroviral pol genes. A protein databank search revealed 22% to 25% identity with the reverse transcriptase domains of retrotransposons. This region also shows the pattern of invariant amino acid residues which are most conserved in retroviral reverse transcriptases. In ORF2 an integrase specific ‘cys’ motif and a conserved sequence of retroviral proteases were identified. Structural similarities with LINE-like elements suggest that the LOA element represents a new non-LTR retrotransposon.

The DNA sequences of the LOA elements 5.I, 5.II 10 and the consensus sequence have been submitted to the EMBL data library with accession numbers X60174, X60175, X60176 and X60177 respectively.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • BesanskyN., 1990. A retrotransposable element from the mosquito Anopheles gambiae. Mol. Cell. Biol. 10: 863–871.

    Google Scholar 

  • CabotE. L. & BeckenbachA. T., 1989. Simultaneous editing of multiple nucleic acid and protein sequences with ESEE. Computer Applications in the Biosciences 5: 233–234.

    Google Scholar 

  • DiNoceraP. P. & CasariG., 1987. Related polypeptides are encoded by Drosophila F elements, I factors and mammalian L1 sequences. Proc. Natl. Acad. Sci. USA 84: 5843–5847.

    Google Scholar 

  • DiNoceraP. P., GrazianiF. & LarvornaG., 1986. Genomic and structural organisation of Drosophila melanogaster G elements. Nucleic Acids Res. 14: 675–691.

    Google Scholar 

  • FanningT. G. & SingerM. F., 1987. LINE-1: a mammalian transposable element. Biochim. Biophys. Acta 910: 203–212.

    Google Scholar 

  • FawcettD. H., ListerC. K., KellettE. & FinneganD. J., 1986. Transposable elements controlling I-R hybrid dysgenesis in D. melanogaster are similar to mammalian LINEs. Cell 47: 1007–1015.

    Google Scholar 

  • HenikoffS., 1985. Unidirectional digestion with exonuclease III creates targeted breakpoints for DNA sequencing. Gene 28: 351–359.

    Google Scholar 

  • HuntJ. A., BishopIIIJ. G. & CarsonH. L., 1984. Chromosomal mapping of a middle-repetitive DNA sequence in a cluster of five species of Hawaiian Drosophila. Procl. Natl. Acad. Sci. USA 81: 7146–7150.

    Google Scholar 

  • HutchisonIIIC. A., HardiesS. C., LoebD. D., SheheeW. R. & EdgellM. H., 1989. LINEs and related retroposons: Long interspersed repeated sequences in the eukaryotic genome. pp. 593–617. In: Mobile DNA, edited by D. E.Berg, and M. M.Howe. American Society for Microbiology, Washington D. C.

    Google Scholar 

  • JakubczakJ. L., XiongY. & EickbushT. H., 1990. Type I (R1) and type II (R2) ribosomal DNA insertions of Drosophila melanogaster are retrotransposable elements closely related to those of Bombyx mori. J. Mol. Biol. 212: 37–52.

    Google Scholar 

  • KimmelB. E., ole-MoiyoiO. K. & YoungJ. R., 1987. Ingi a 5.2 kilobase dispersed sequence element from Trypanosoma brucei. Mol. Cell. Biol. 7: 1465–1475.

    Google Scholar 

  • KozakM., 1986. Point mutations define a sequence flanking the AUG initiation codon that modulates translation by eukaryotic ribosomes. Cell 44: 283–292.

    Google Scholar 

  • LoebD. D., PadgettR. W., HardiesS. C., SheheeW. R., ComerM. B., EdgellM. H. & HutchisonIIIC. A., 1986. The sequence of a large L1Md element reveals a tandemly repeated 5′ end and several features found in retrotransposons. Mol. Cell. Biol. 6: 168–182.

    Google Scholar 

  • MarckC., 1986. Fast analysis of DNA and protein sequence on the Apple IIe: Restriction sites search, alignments of short sequences and dot matrix analysis. Nucleic Acids Res. 14: 583–590.

    Google Scholar 

  • MeadD. A. & KemperB., 1988. Chimeric single-stranded DNA phage-plasmid cloning vectors. pp. 85–102. In: Vectors—A Survey of Molecular Cloning Vectors and their Uses, edited by R. L.Rodriguez, and D. T.Denhardt, Butterworths Publishers Boston, M. A.

    Google Scholar 

  • PearlL. H. & TaylorW. R., 1987. A structural model for the retroviral proteases. Nature 329: 351–354.

    Google Scholar 

  • PearsonW. R. & LipmanD. J., 1988. Improved tools for biological sequence comparison. Proc. Natl. Acad. Sci. USA 85: 2444–2448.

    Google Scholar 

  • PriimaegiA. F., MizrokhiL. J. & IlynY. V., 1988. The Drosophila mobile element jockey belongs to LINEs and contains coding sequences homologous to some retroviral proteins. Gene 70: 253–262.

    Google Scholar 

  • SangerF., NicklenS. & CoulsonA. R., 1977. DNA sequencing with chain-terminating inhibitors. Proc. Natl. Acad. Sci. USA 74: 5463–5467.

    Google Scholar 

  • TohH., KikunoR., HayashidaH., MiyataT., KugimiyaW., InouyeS., YukiS. & SaigoK., 1985. Close structural resemblance between putative polymerase of a Drosophila transposable genetic element 17.6 and pol gene product of Moloney murine leukemia virus. EMBO J. 4: 1267–1272.

    Google Scholar 

  • VarmusH. & BrownP., 1989. Retroviruses. pp. 53–108. In BergD. and HoweM. (eds.), Mobile DNA, edited by D. E. Berg, and M. M. Howe. American Society for Microbiology, Washington D. C.

    Google Scholar 

  • XiongY. & EickbushT. H., 1988. The site-specific ribosomal DNA insertion element R1Bm belongs to a class of non-longterminal-repeat retrotransposons. Mol. Cell. Biol. 8: 114–123.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Felger, I., Hunt, J.A. A non-LTR retrotransposon from the Hawaiian Drosophila: the LOA element. Genetica 85, 119–130 (1992). https://doi.org/10.1007/BF00120318

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00120318

Keywords

Navigation