[1]Thibault S T, Singer M A, Miyazaki W Y, Milash B, Dompe N A, Singh C M, Buchholz R, Demsky M, Fawcett R, Francis-Lang H L, Ryner L, Cheung L M, Chong A, Erickson C, Fisher W W, Greer K, Hartouni S R, Howie E, Jakkula L, Joo D, Killpack K, Laufer A, Mazzotta J, Smith R D, Stevens L M, Stuber C, Tan L R, Ventura R, Woo A, Zakrajsek I, Zhao L, Chen F, Swimmer C, Kopczynski C, Duyk G, Winberg M L, Margolis J. A complementary transposon tool kit for Drosophila melanogaster using P and piggyBac. Nature Genetics, 2004, 36(3): 283-287.
[2]Handler A M, McCombs S D, Fraser M J, Saul S H. The lepidopteran transposon vector, piggyBac, mediates germ-line transformation in the Mediterranean fruit fly. Proceedings of the National Academy of Sciences of the United States of America, 1998, 95: 7520-7525.
[3]Loukeris T G, Livadaras I, Arcà B, Zabalou S, Savakis C. Gene transfer into the medfly, Ceratitis capitata, with a Drosophila hydei transposable element. Science, 1995, 270: 2002-2005.
[4]Coates C J, Jasinskiene N, Miyashiro L, James A A. Mariner transposition and transformation of the yellow fever mosquito, Aedes aegypti. Proceedings of the National Academy of Sciences of the United States of America, 1998, 95: 3748-3751.
[5]Jasinskiene N, Coates C J, Benedict M Q, Cornel A J, Rafferty C S, James A A, Collins F H. Stable transformation of the yellow fever mosquito, Aedes aegypti, with the Hermes element from the housefly. Proceedings of the National Academy of Sciences of the United States of America, 1998, 95: 3743-3747.
[6]Handler A M, Harrell Ⅱ R A. Transformation of the Caribbean fruit fly, Anastrepha suspensa, with a piggyBac vector marked with polyubiquitin-regulated GFP. Insect Biochemistry and Molecular Biology, 2001, 31: 199-205.
[7]Gomez S P, Handler A M. A Drosophila melanogaster hobo-white+ vector mediates low frequency gene transfer in D. virilis with full interspecific white+ complementation. Insect Molecular Biology, 1997, 6(2): 165-171.
[8]Lohe A R, Hartl D L. Germline transformation of Drosophila virilis with the transposable element mariner. Genetics, 1996, 143: 365-374.
[9]Toshiki T, Chantal T, Corinne R, Toshio K, Eappen A, Mari K, Natuo K, Jean-Luc T, Bernard M, Gérard C, Paul S, Malcolm F, Jean-Claude P, Pierre C. Germline transformation of the silkworm Bombyx mori L. using a piggyBac transposon-derived vector. Nature Biotechnology, 2000, 18: 81-84.
[10]Thomas J L, Da Rocha M, Besse A, Mauchamp B, Chavancy G. 3xP3-EGFP marker facilitates screening for transgenic silkworm Bombyx mori L. from the embryonic stage onwards. Insect Biochemistry and Molecular Biology, 2002, 32: 247-253.
[11]Tomita M, Munetsuna H, Sato T, Adachi T, Hino R, Hayashi M, Shimizu K, Nakamura N, Tamura T, Yoshizato K. Transgenic silkworms produce recombinant human type III procollagen in cocoons. Nature Biotechnology, 2003, 21: 52-56.
[12]Uhlí?ová M, Asahina M, Riddiford L M, Jindra M. Heat-inducible transgenic expression in the silkmoth Bombyx mori. Development Genes and Evolution, 2002, 212: 145-151.
[13]Abe H, Ohbayashi F, Sugasaki T, Kanehara M, Terada T, Shimada T, Kawai S, Mita K, Kanamori Y, Yamamoto M T, Oshiki T. Two novel Pao-like retrotransposons (Kamikaze and Yamato) from the silkworm species Bombyx mori and B. mandarina: common structural features of Pao-like elements. Molecular Genetics and Genomics, 2001, 265: 375-385.
[14]Xiong Y, Burke W D, Eickbush T H. Pao, a highly divergent retrotransposable element from Bombyx mori containing long terminal repeats with tandem copies of the putative R region. Nucleic Acids Research, 1993, 21(9): 2117-2123.
[15]Feng Q, Schumann G, Boeke J D. Retrotransposon R1Bm endonuclease cleaves the target sequence. Proceedings of the National Academy of Sciences of the United States of America, 1998, 95: 2083-2088.
[16]Bibillo A, Eickbush T H. The reverse transcriptase of the R2 non-LTR retrotransposon: continuous synthesis of cDNA on non-continuous RNA templates. Journal of Molecular Biology, 2002, 316: 459-473.
[17]Luan D D, Korman M H, Jakubczak J L, Eickbush T H. Reverse transcription of R2Bm RNA is primed by a nick at the chromosomal target site: a mechanism for non-LTR retrotransposition. Cell, 1993, 72: 595-605.
[18]Ichimura S, Mita K, Sugaya K. A major non-LTR retrotransposon of Bombyx mori, L1Bm. Journal of Molecular Evolution, 1997, 45: 253-264.
[19]Robertson H M, Asplund M L. Bmmar1: a basal lineage of the mariner family of transposable elements in the silkworm moth, Bombyx mori. Insect Biochemistry and Molecular Biology, 1996, 26(8/9): 945-954.
[20]Robertson H M, Walden K K. Bmmar6, a second mori subfamily mariner transposon from the silkworm moth Bombyx mori. Insect Molecular Biology, 2003, 12(2): 167-171.
[21]Mikitani K, Sugasaki T, Shimada T, Kobayashi M, Gustafsson J A. The chitinase gene of the silkworm, Bombyx mori, contains a novel Tc-like transposable element. The Journal of Biological Chemistry, 2000, 275(48): 37725-37732.
[22]Osanai-Futahashi M, Suetsugu Y, Mita K, Fujiwara H. Genome-wide screening and characterization of transposable elements and their distribution analysis in the silkworm, Bombyx mori. Insect Biochemistry and Molecular Biology, 2008, 38: 1046-1057.
[23]Kempken F, Windhofer F. The hAT family: a versatile transposon group common to plants, fungi, animals, and man. Chromosoma, 2001, 110: 1-9.
[24]Döring H P, Starlinger P. Molecular genetics of transposable elements in plants. Annual Review of Genetics, 1986, 20: 175-200.
[25]Craig N L. Target site selection in transposition. Annual Review of Biochemistry, 1997, 66: 437-474.
[26]Labrador M, Corces V G. Transposable element-host interactions: regulation of insertion and excision. Annual Review of Genetics, 1997, 31: 381-404. |