Transposable Elementmediated Transgenesis in Insects Beyond Drosophila

Journal of Neurogenetics

Volumn 15, Issue 42067, 2001, Pages 179-192

  Kimura, Kiyoshi ^a  

^a NATIONAL INSTITUTE OF LIVESTOCK AND GRASSLAND SCIENCE   (Japan)

Author keywords

Germ line transformation; honeybee; microinjection; transposable elements

Indexed keywords

DNA;

DROSOPHILA; FLY; GENE TARGETING; GENETIC TRANSFORMATION; GERM LINE; HONEYBEE; INSECT CONTROL; NONHUMAN; PRIORITY JOURNAL; REVIEW; SPECIES IDENTIFICATION; TRANSGENICS; TRANSPOSON;

ANIMALS; BEES; DNA TRANSPOSABLE ELEMENTS; GENE TRANSFER TECHNIQUES; GENES, INSECT; INSECTS; MICROINJECTIONS; TRANSFORMATION, GENETIC; TRANSGENES;

APIS MELLIFERA; DIPTERA; HEXAPODA; INSECTA; TRANSPOSONS;

EID: 0035738150     PISSN: 01677063     EISSN: 15635260     Source Type: Journal    
DOI: 10.3109/01677060109167375     Document Type: Article

References (60)

1. Atkinson P.W., Pinkerson A.C., O'Brochta D.A. Genetic transformation systems in insects. Annu. Rev. Entomol. 2001; 46: 317 – 346
2. Atkinson P.W., Warren W.D., O'Brochta D.A. The hobo transposable element of Drosophila can be cross-mobilized in houseflies and excises like the Ac element of maize. Proc. Natl. Acad. Sci. USA 1993; 90: 9693 – 9697
3. Baldarelli R.M., Lengyel J.A. Transient expression of DNA after ballistic introduction into Drosophila embryos. Nucl. Acids Res. 1990; 18: 5903 – 5904
4. Berghammer A.J., Klingler M., Wimmer E.A. A universal marker for transgenic insects. Nature 1999; 402: 370 – 371
5. Bessereau J.L., Wright A., Williams D.C., Schuske K., Davis M.W., Jorgensen E.M. Mobilization of a Drosophila transposon in the Caenorhabditis elegans germ line. Nature 2001; 413: 70 – 74
6. Calvi B.R., Hong T.J., Findley S.D., Gelbart W.M. Evidence for a common evolutionary origin of inverted repeat transposons in Drosophila and plants: hobo, Activator, and. Tam3. Cell 1991; 66: 465 – 471
7. Cary L.C., Goebel M., Corsaro H.H., Wang H.H., Rosen E., Fraser M.J. Transposon mutagenesis of baculoviruses: Analysis of Trichoplusia ni transposon IFP2 inserions within the FP-Locus of nuclear polyhedrosis viruses. Virology 1989; 161: 8 – 17
8. Catteruccia F., Nolan T., Blass C., Muller H.-M., Crisanti A., Kafatos F.C., Loukeris T. G. Toward Anopheles transformation: Minos element activity in anopheline cells and embryos. Proc. Natl. Acad. Sci. USA 2000; 97: 2157 – 2162
9. Catteruccia F., Nolan T., Loukeris T.G., Blass C., Savakis C., Kafatos F.C., Crisanti A. Stable germline transformation of the malaria mosquito. Anopheles Stephensi. Nature 2000; 405: 959 – 962
10. Coates C. J., Jasinskiene N., Miyashiro L., James A. A. Mariner transposition and transformation of the yellow fever mosquito. Aedes aegypti. Proc. Natl. Acad. Sci. USA 1998; 95: 3742 – 3751
11. DuPraw E.J. A unique hatching process in the honeybee. Trans. Am. Microscop. Soc. 1961; 80: 185 – 190
12. DuPraw E.J. The honeybee embyo. Methods in Developmental Biology, F.H. Wilt, N. K. Wessels. Crowell, New York 1967; 183 – 217
13. Fadool J.M., Hartl D.L., Dowling J.E. Transposition of the mariner element from Drosophila mauritiana in zebrafish. Proc. Natl. Acad. Sci. USA 1998; 95: 5182 – 5186
14. Franz G., Loukeris T.G., Dialektaki G., Thompson C.R.L., Savakis C. Mobile Minos elements from Drosophila hydei encode a two-exon transposase with similarity to the paired DNA-binding domain. Proc. Natl. Acad. Sci. USA 1994; 91: 4746 – 4750
15. Franz G., Savakis C. Minos, a new transposable element from Drosophila hydei, is a member of the Tcl-like family of transposons. Nucl. Acids Res. 1991; 19: 6646
16. Fraser M.J., Smith G.E., Summers M.D. Acquisition of host-cell DNA-sequences by baculoviruses - relationship between host DNA insertions and FP mutants of Autographa-californica and Galleria-mellonella nuclear polyhedrosis viruses. J. Virol. 1983; 47: 287 – 300
17. Gueiros-Filho F.J., Beverley S.M. Trans-kingdom transposition of the Drosophila element mariner within the protozoan. Leishmania. Science 1997; 276: 1716 – 1719
18. Handler A.M. A current perspective on insect gene transformation. Insect Biochem. Molec. Biol. 2001; 31: 111 – 128
19. Handler A.M., Harreil R.A. Transformation of the Caribbean fruit fly, Anastrepha suspensa, with piggy Bac vector marked with polyubiquitin-regulated GFP. Insect Biochem. Molec. Biol. 2001; 31: 199 – 205
20. Insect Transgenesis, A.A. James, A.M. Handler. CRC Press, Boca Raton, FL 2000
21. Handler A.M., McCombs S.D. The piggy Bac transposon mediates germ-line transformation in the Oriental fruit fly and closely related elements exist in its genome. Insect Molec. Biol. 2000; 9: 605 – 612
22. Handler A.M., McCombs S.D., Fraser M.J., Saul S.H. The lepidopteran transposon vector, piggy Bac, mediates germline transformation in the Mediterranean fruitfly. Proc. Natl. Acad. Sci. USA 1998; 95: 7520 – 7525
23. Harbo J.R. Instrumental insemination of queen bees. Am. Bee J. 1985; 125: 282 – 287
24. Hediger M., Niessen M., Wimmer E.A., Dübendorfer A., Bopp D. Genetic transformation of the housefly Musca domestica with the lepidopteran derived transposon. piggy Bac. Insect. Molec. Biol. 2001; 10: 113 – 119
25. Jacobson J.W., Medlhora M.M., Hartl D.L. Molecular structure of somatically unstable transposable element in Drosophila. Proc. Natl. Acad. Sci. USA. 1986; 83: 8684 – 8688
26. Jasinskiene N., Coates C.J., Benedict M.Q., Cornel A.J., Rafferty C.S., James A.A., Collins F. H. Stable transposon mediated transformation of the yellow fever mosquito, Aedes aegypti, using the Hermes element from the housefly. Proc. Natl. Acad. Sci. USA. 1998; 95: 3743 – 3747
27. Jasinskiene N., Coates C.J., James A.A. Structure of Hermes integrations in the germline of the yellow fever mosquito. Aedes aegypti. Insect Molec. Biol. 2000; 9: 11 – 18
28. Kamdar P., Von Allmen G., Finnerty V. Transient expression of DNA in Drosophila via electroporation. Nuc. Acids Res. 1992; 11: 3526
29. Klinakis A.G., Loukeris T.G., Pavlopoulos A., Savakis C. Mobility assays confirm the broad host-range activity of the Minos transposable element and validate new transformation tools. Insect Molec. Biol. 2000; 9: 269 – 276
30. Klinakis A.G., Zagoraiou L., Vassilatis D.K., Savakis C. Genome-wide insertional mutagenesis in human cells by the Drosophila mobile element. Minos. EMBO Rep. 2000; 1: 416 – 421
31. Kokoza V., Ahmed A., Cho W.-L., Jasinskiene N., James A.A. Engineering blood meal-activated systemic immunity in the yellow fever masquito. Aedes aegypti. Proc. Natl. Acad. Sci. USA 2000; 97: 9144 – 9149
32. Kokoza V., Ahmed A., Wimmer E.A., Raikhel A. S. Efficient transformation of the yellow fever mosquito Aedes aegypti using the piggy Bac transposable element vevtor pBac[3xP3-EGFP afm]. Insect Biochem. Molec. Biol. 2001; 31: 1137 – 1143
33. Lampe D.J., Akerley B.J., Rubin E.J., Mekalanos J.J., Robertson H.M. Hyperactive transposase mutants of the Himar 1 mariner transposon. Proc. Natl. Acad. Sci. USA 1999; 96: 11428 – 11433
34. Lampe D.J., Churchill M.E., Robertson H. M. A purified mariner transposase is sufficient to mediate transposition. in vitro. EMBO J. 1996; 15: 5470 – 5479
35. Lampe D.J., Grant T.E., Robertson H. M. Factors affecting transposition of the Himar1 mariner transposon. in vitro. Genetics 1998; 149: 179 – 187
36. Lohe A.R., Hartl D.L. Germline transformation of Drosophila virilis with the transposable element. mariner. Genetics 1996; 143: 365 – 374
37. Lohe A.R., Hartl D.L. Autoregulation of mariner transposase activity by overproduction and dominant-negative complementation. Molec. Biol. Evol. 1996; 13: 549 – 555
38. Loukeris T.G., Livadaras I., Area B., Zabalou S., Savakis C. Gene transfer into the Medfly, Ceratitis capitata, with a Drosophila hydei transposable element. Science 1995; 270: 2002 – 2005
39. Lozovskaya E.R., Nurminsky D.I., Hartl D.L., Sullivan D.T. Germline transformation of Drosophila virilis mediated by the transposable element hobo. Genetics 1996; 142: 173 – 177
40. Luo G., Ivies Z., Izsvák Z., Bradley A. Chromosomal transposition of a Tel/mariner-like element in mouse embryonic stem cells. Proc. Natl. Acad. Sci. USA 1998; 95: 10796 – 10773
41. O'Brochta D.A., Atkinson P.W. Transposable elements and gene transformation in non-drosophilids. Insect Biochem. Molec. Biol. 1996; 26: 739 – 753
42. O'Brochta D.A., Atkinson P.W., Lehane M.J. Transformation of Stomoxys calcitrans with a Hermes gene vector. Insect Molec. Biol. 2000; 9: 531 – 538
43. Pelicic V., Morelle S., Lampe D., Nassif X. Mutagenesis of Neisseria meningitidis by in vitro transposition of. Himar1 mariner. J Bacteriol. 2000; 182: 5391 – 5398
44. Peloquin J.J., Thibault S.T., Staten R., Miller T.A. Germ-line transformation of pink bollworm (Lepidoptera: Gelechiidae) mediated by the piggy Bac transposable element. Insect Molec. Biol. 2000; 9: 323 – 333
45. Presnail J.K., Hoy M.A. Stable transformation of a benefical arthropod, Mataseiulus occidebtalis (Acari:Phytoseiidae), by microinjection technique. Proc. Natl. Acad. Sci. USA 1992; 89: 7732 – 7736
46. Rio D.C., Rubin G.M. Identification and purification of a Drosophila protein that binds to the terminal 31-base-pair inverted repeats if the transposable element. Proc. Natl. Acad. Sci. USA 1988; 85: 8929 – 8933
47. Robertson H.M. The mariner transposable element is widespread in insects. Nature 1993; 362: 241 – 245
48. Robertson H.M., Lampe D.J. Distribution of transposable elements in arthropods. Annu. Rev. Entomol. 1995; 40: 333 – 357
49. Robinson K.O., Ferguson H.J., Cobey S., Vaessin H., Smith B.H. Sperm-mediated transformation of the honey bee. Apis mellifera. Insect Molec. Biol. 2000; 9: 625 – 634
50. Rubin G.M., Spradling A.C. Genetic transformation of Drosophila with transposable element vectors. Science 1982; 218: 348 – 353
51. Sherman A., Dawson A., Mather C., Gilhooley H., Li Y., Mitchell R., Finnegan D., Sang H. Transposition of the Drosophila element mariner into the chicken germ line. Nature Biotech. 1998; 16: 1050 – 1053
52. Shull R.W., Dixson S.E. An artificial diet for laboratory rearing of honeybees. J. Apic. Res. 1986; 25: 35 – 43
53. Spradling A.C. P element-mediated transformation. Drosophila: A Practical Approach, D.B. Roberts. IRL Press, Oxford 1986; 175 – 197
54. Sundararajan P., Atkinson P.W., O'Brochta D.A. Transposable element interactions in insects: crossmobilization of hobo and. Hermes. Insect Molec. Biol. 1999; 8: 359 – 368
55. Tamura T., Thibert T., Royer C., Kanda T., Eappen A., Kamba M., Komoto N., Thomas J.-L., Mauchamp B., Chavancy G., Shirk P., Fraser M., Prud'homme J.-C., Couble P. A piggy Bac element-derived vector efficiently promotes germ-line transformation in the silkworm. Bombyx mort L. Nature Biotech. 2000; 18: 81 – 84
56. Wang W., Swevers L., Iatou K. mariner(Mos1) transposase and genomic integration of foreign gene sequence in Bombyx mori cells. Insect Molec. Biol. 2000; 9: 145 – 155
57. Warren W.D., Atkinson P.W., O'Brochta D.A. The Hermes transposable element from the house fly, Musca domestica, is a short inverted repeat-type element of the hobo, Ac, and Tam3 (hAT) element family. Genet. Res. Camb. 1994; 64: 87 – 97
58. Zagoraiou L., Drabek D., Alexaki S., Guy J.A., Klinakis A.G., Langeveld A., Skavdis G., Mamalaki C., Grosveld F., Savakis C. In vivo transposition of Minos, a Drosophila mobile element, in mammalian tissues. Proc. Natl. Acad. Sci. USA 2001; 98: 11474 – 11478
59. Zhang J.K., Pritchett M.A., Lampe D.J., Robertson H. M., Metcalf W.W. In vivo transposon mutagenesis of the methanogenic archaeon Methanosarcina acetivorans C2A using a modified version of the insect manner-family transposable element. Himar1. Proc. Natl. Acad. Sci. USA 2000; 97: 9665 – 9670
60. Yoshiyama M., Honda H., Kimura K. Successful transformation of the housefly, Musca domestica (Diptera:Muscidae) with the transposable element. mariner. Appl. Entomol. Zool. 2000; 35: 321 – 325