Skip to main content
Log in

An abundant LINE-like element amplified in the genome of Lilium speciosum

  • Published:
Molecular and General Genetics MGG Aims and scope Submit manuscript

Summary

The genomes of Lilium species are very large, containing 30–40 million kilobase pairs of DNA. An abundant fragment of 3.5 kb was released by BamHI digestion of genomic DNA of Lilium speciosum. Analysis of 20 genomic clones containing sequences homologous to the fragment showed it to be part of a 4.45 kb dispersed repeat, which was named del2. Sequence analysis of one full element and regions of four others revealed del2 to be a non-LTR (long terminal repeat) retrotransposon. It is flanked by short direct repeats of from 4 to 13 bp and a run of adenines occurs at one end (the proposed 3′ end), 63 by downstream from a polyadenylation signal. A possible RNA polymerase II promoter similar to that found in Drosophila I and F group elements is present internally 30 by downstream from the 5′ end. Two degenerate open reading frames (ORFs) are present, the 5′ ORF containing a gag-related cysteine motif, and the 3′ ORF containing a different cysteine motif also found in most non-LTR retrotransposons. The 3′ ORF also has regions with homology to reverse transcriptase sequences, which are most similar to those in Cin4 of maize, the Ll LINE elements of humans and mice and the R2 ribosomal DNA inserts of insects. The majority of del2 elements occur as the full 4.45 kb element. They account for an estimated 4 % of the L. speciosum genome and are present in approximately 250 000 copies. del2-related sequences were also detected in 12 other monocot species. del2 is the most abundant non-LTR retrotransposon identified so far and reveals that LINE-like elements have been greatly amplified in some plant genomes just as they have in mammals.

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

  • Besansky NJ (1990) A retrotransposable element from the mosquito Anopheles gambiae. Mol Cell Biol 10:863–871

    Google Scholar 

  • Bucheton A (1990) I transposable elements and I-R hybrid dysgenesis in Drosophila. Trends Genet 6:16–21

    Google Scholar 

  • Burke WD, Calalang CC, Eickbush TH (1987) The site-specific ribosomal insertion element type II of Bombyx mori (R2Bm) contains the coding sequence for a reverse transcriptase-like enzyme. Mol Cell Biol 7:2221–2230

    Google Scholar 

  • Burton FH, Loeb DD, Voliva CF, Martin SL, Edgell MH, Hutchinson CA (1986) Conservation throughout Mammalia and extensive protein encoding capacity of the highly repeated DNA long interspersed sequence one. J Mol Biol 187:291–304

    Google Scholar 

  • Covey SN (1986) Amino acid sequence homology in gag region of reverse transcribing elements and the coat protein gene of cauli-flower mosaic virus. Nucleic Acids Res 14:623–633

    Google Scholar 

  • Di Nocera PP (1988) Close relationship between non-viral retroposons in Drosophila melanogaster. Nucleic Acids Res 16:4041–4052

    Google Scholar 

  • Di Nocera PP, Casari G (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 

  • Evans JP, Palmiter RD (1991) Retrotransposition of a mouse L1 element. Proc Natl Acad Sci USA 88:8792–8795

    Google Scholar 

  • Fanning T, Singer M (1987) The LINE-1 DNA sequences in four mammalian orders predict proteins that conserve homologies in retrovirus proteins. Nucleic Acids Res 15:2251–2260

    Google Scholar 

  • Fawcett DH, Lister CK, Kellett E, Finnegan DJ (1986) Transposable elements controlling I-R hybrid dysgenesis in D. melanogaster are similar to mammalian LINEs. Cell 47:1007–1015

    Google Scholar 

  • Finnegan DJ (1989) The I factor and I-R hybrid dysgenesis in Drosophila melanogaster. In: Berg DE, Howe MM (eds) Mobile DNA. American Society for Microbiology, Washington DC, pp 503–517

    Google Scholar 

  • Friedman BE, Bouchard RA, Stern H (1982) DNA sequences repaired at pachytene exhibit strong homology among distantly related plants. Chromosoma 87:409–424

    Google Scholar 

  • Garrett JE, Knutzon DS, Carroll D (1989) Composite transposable element in the Xenopus laevis genome. Mol Cell Biol 9:3018–3027

    Google Scholar 

  • Hutchinson CA, Hardies SC, Loeb DD, Shehee WR, Edgell MH (1989) LINEs and related retrotransposons: long interspersed repeated sequences in the eucaryotic genome. In: Berg DE, Howe MM (eds) Mobile DNA. American Society for Microbiology, Washington DC, pp 593–617

    Google Scholar 

  • Ivanov VA, Melnikov AA, Siunov AV, Fodor II, Ilyin YV (1991) Authentic reverse transcriptase is encoded by jockey mobile Drosophila element related to mammalian LINEs. EMBO J 10:2489–2495

    Google Scholar 

  • Jakubczak JL, Xiong Y, Eickbush TH (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 

  • Jakubczak JL, Burke WD, Eickbush TH (1991) Retrotransposable elements R1 and R2 interrupt the rRNA genes of most insects. Proc Natl Acad Sci USA 88:3295–3299

    Google Scholar 

  • Jensen S, Heidmann T (1991) An indicator gene for detection of germline retrotransposition in transgenic Drosophila demonstrates RNA-mediated transposition of the LINE I element. EMBO J 10:1927–1937

    Google Scholar 

  • Joseph JL, Sentry JW, Smyth DR (1990) Interspecies distribution of abundant DNA sequences in Lilium. J Mol Evol 30:146–154

    Google Scholar 

  • Kimmel BE, Ole-Moiyol OK, Young JR (1987) Ingi, a 5.2-kb dispersed sequence element from Trypanosoma brucei that carries half a smaller mobile element at either end and has homology with mammalian LINES. Mol Cell Biol 7:1465–1475

    Google Scholar 

  • Mathias SL, Scott AF, Kazazian HH, Boeke JD, Gabriel A (1991) Reverse transcriptase encoded by a human transposable element. Science 254:1808–1810

    Google Scholar 

  • Minchiotti G, Di Nocera PP (1991) Convergent transcription initiates from oppositely oriented promoters within the 5′ end regions of Drosophila melanogaster F elements. Mol Cell Biol 11:5171–5180

    Google Scholar 

  • Mizrokhi LJ, Georgieva SG, Ilyin YV (1988) jockey, a mobile Drosophila element similar to mammalian LINEs, is transcribed from the internal promoter by RNA polymerase II. Cell 54:685–691

    Google Scholar 

  • Murphy NB, Pays A, Tebabi P, Coquelet H, Guyaux M, Steinert M, Pays E (1987) Trypanosoma brucei repeated element with unusual structural and transcriptional properties. J Mol Biol 195:855–871

    Google Scholar 

  • O'Hare K, Alley MRK, Cullingford TE, Driver A, Sanderson MJ (1991) DNA sequence of the Doe retroposon in the white-1 mutant of Drosophila melanogaster and of secondary insertions in the phenotypically altered derivatives white-honey and white-eosin. Mol Gen Genet 225:17–24

    Google Scholar 

  • Pélisson A, Finnegan DJ, Bucheton A (1991) Evidence for retrotransposition of the I factor, a LINE element of Drosophila melanogaster. Proc Natl Acad Sci USA 88:4907–4910

    Google Scholar 

  • Priimägi AF, Mizrokhi LJ, Ilyin YV (1988) The Drosophila mobile element jockey belongs to LINEs and contains coding sequences homologus to some retroviral proteins. Gene 70:253–262

    Google Scholar 

  • Sambrook J, Fritsch EF, Maniatis T (1989) Molecular cloning: A laboratory manual, 2nd edn. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York

    Google Scholar 

  • Schwarz-Sommer Z, Leclercq L, Göbel E, Saedler H (1987) Cin4, an insert altering the structure of the A1 gene in Zea mays, exhibits properties of nonviral retrotransposons. EMBO J 6:3873–3880

    Google Scholar 

  • Sentry JW, Smyth DR (1985) A family of repeated sequences dispersed through the genome of Lilium henryi. Chromosoma 92:149–155

    Google Scholar 

  • Sentry JW, Smyth DR (1989) An element with long terminal repeats and its variant arrangements in the genome of Lilium henryi. Mol Gen Genet 215:349–354

    Google Scholar 

  • Smyth DR, Kalitsis P, Joseph JL, Sentry JW (1989) Plant retrotransposon from Lilium henryi is related to Ty3 of yeast and the gypsy group of Drosophila. Proc Natl Acad Sci USA 86:5015–5019

    Google Scholar 

  • Swergold GD (1990) Identification, characterization, and cell specificity of a human LINE-1 promoter. Mol Cell Biol 10:6718–6729

    Google Scholar 

  • Xiong Y, Eickbush TH (1988) The site-specific ribosomal DNA insertion element R1 Bm belongs to a class of non-long-terminalrepeat retrotransposons. Mol Cell Biol 8:114–123

    Google Scholar 

  • Xiong Y, Eickbush TH (1990) Origin and evolution of retroelements based upon their reverse transcriptase sequences. EMBO J 9:3353–3362

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by D. Finnegan

Rights and permissions

Reprints and permissions

About this article

Cite this article

Leeton, P.R.J., Smyth, D.R. An abundant LINE-like element amplified in the genome of Lilium speciosum . Molec. Gen. Genet. 237, 97–104 (1993). https://doi.org/10.1007/BF00282789

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00282789

Key words

Navigation