Construction and characterization of new piggyBac vectors for constitutive or inducible expression of heterologous gene pairs and the identification of a previously unrecognized activator sequence in piggyBac

BackgroundWe constructed and characterized several new piggyBac vectors to provide transposition of constitutively- or inducibly-expressible heterologous gene pairs. The dual constitutive control element consists of back-to-back copies of a baculovirus immediate early (ie1) promoter separated by a baculovirus enhancer (hr5). The dual inducible control element consists of back-to-back copies of a minimal cytomegalovirus (CMVmin) promoter separated by a synthetic operator (TetO7), which drives transcription in the presence of a mutant transcriptional repressor plus tetracycline.ResultsCharacterization of these vectors revealed an unexpected position effect, in which heterologous genes adjacent to the 3'- terminal region ("rightward" genes) were consistently expressed at higher levels than those adjacent to the 5'-terminal region ("leftward" genes) of the piggyBac element. This position effect was observed with all six heterologous genes examined and with both transcriptional control elements. Further analysis demonstrated that this position effect resulted from stimulation of rightward gene expression by the internal domain sequence of the 3'-terminal region of piggyBac. Inserting a copy of this sequence into the 5'- terminal repeat region of our new piggyBac vectors in either orientation stimulated leftward gene expression. Representative piggyBac vectors designed for constitutive or inducible expression of heterologous gene pairs were shown to be functional as insect transformation vectors.ConclusionThis study is significant because (a) it demonstrates the utility of a strategy for the construction of piggyBac vectors that can provide constitutive or inducible heterologous gene pair expression and (b) it reveals the presence of a previously unrecognized transcriptional activator in piggyBac, which is an important and increasingly utilized transposable element.

[1]  Thomas A Kost,et al.  Baculovirus as versatile vectors for protein expression in insect and mammalian cells , 2005, Nature Biotechnology.

[2]  I. Kirsch,et al.  Bovine galactosyltransferase: identification of a clone by direct immunological screening of a cDNA expression library. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[3]  W. Hillen,et al.  Tetracycline-inducible systems for Drosophila , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[4]  C. Sim,et al.  Molecular evolutionary analysis of the widespread piggyBac transposon family and related "domesticated" sequences , 2003, Molecular Genetics and Genomics.

[5]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[6]  M. Fraser,et al.  High-efficiency transformation of Plasmodium falciparum by the lepidopteran transposable element piggyBac. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[7]  G. Rubin,et al.  Genetic transformation of Drosophila with transposable element vectors. , 1982, Science.

[8]  C. Bauser,et al.  Excision of the piggyBac transposable element in vitro is a precise event that is enhanced by the expression of its encoded transposase , 1996, Genetica.

[9]  L. Warren,et al.  The thiobarbituric acid assay of sialic acids. , 1959, The Journal of biological chemistry.

[10]  Young-Choon Lee,et al.  Mouse β-galactoside α2,3-sialyltransferases: comparison of in vitro substrate specificities and tissue specific expression , 1997 .

[11]  D. Jarvis,et al.  Immediate-early baculovirus vectors for foreign gene expression in transformed or infected insect cells. , 1996, Protein expression and purification.

[12]  J. Lofgren,et al.  Engineering Chinese hamster ovary cells to maximize sialic acid content of recombinant glycoproteins , 1999, Nature Biotechnology.

[13]  C. Bauser,et al.  Precise excision of TTAA‐specific lepidopteran transposons piggyBac (IFP2) and tagalong (TFP3) from the baculovirus genome in cell lines from two species of Lepidoptera , 1996, Insect molecular biology.

[14]  D. Jarvis,et al.  Developing baculovirus-insect cell expression systems for humanized recombinant glycoprotein production. , 2003, Virology.

[15]  D. Jarvis,et al.  Improved glycosylation of a foreign protein by Tn-5B1-4 cells engineered to express mammalian glycosyltransferases. , 2001, Biotechnology and bioengineering.

[16]  J. Squire,et al.  The human UDP-N-acetylglucosamine: alpha-6-D-mannoside-beta-1,2- N-acetylglucosaminyltransferase II gene (MGAT2). Cloning of genomic DNA, localization to chromosome 14q21, expression in insect cells and purification of the recombinant protein. , 1995, European journal of biochemistry.

[17]  P. Stanley,et al.  Mammalian cytidine 5'-monophosphate N-acetylneuraminic acid synthetase: a nuclear protein with evolutionarily conserved structural motifs. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[18]  F. Rottman,et al.  The 3'-flanking sequence of the bovine growth hormone gene contains novel elements required for efficient and accurate polyadenylation. , 1992, The Journal of biological chemistry.

[19]  M. Gossen,et al.  Transcriptional activation by tetracyclines in mammalian cells. , 1995, Science.

[20]  K. Kitajima,et al.  Molecular cloning and expression of the mouse N-acetylneuraminic acid 9-phosphate synthase which does not have deaminoneuraminic acid (KDN) 9-phosphate synthase activity. , 2000, Biochemical and biophysical research communications.

[21]  H. G. Wang,et al.  Transposon mutagenesis of baculoviruses: analysis of Trichoplusia ni transposon IFP2 insertions within the FP-locus of nuclear polyhedrosis viruses. , 1989, Virology.

[22]  A. Handler,et al.  Insect transgenesis: methods and applications. , 2000 .

[23]  K. McEntee,et al.  Primary structure of beta-galactoside alpha 2,6-sialyltransferase. Conversion of membrane-bound enzyme to soluble forms by cleavage of the NH2-terminal signal anchor. , 1987, The Journal of biological chemistry.

[24]  J. Hollister,et al.  Engineering lepidopteran insect cells for sialoglycoprotein production by genetic transformation with mammalian β1,4-galactosyltransferase and α2,6-sialyltransferase genes , 2001 .

[25]  M. Fraser The TTAA-Specific Family of Transposable Elements: Identification, Functional Characterization, and Utility for Transformation of Insects , 2000 .

[26]  M. Summers,et al.  A Manual of Methods for Baculovirus Vectors and Insect Cell Culture Procedures. , 1987 .

[27]  Min Han,et al.  Efficient Transposition of the piggyBac (PB) Transposon in Mammalian Cells and Mice , 2005, Cell.

[28]  A. Sutton,et al.  Purification, properties, and genetic location of Escherichia coli cytidine 5'-monophosphate N-acetylneuraminic acid synthetase. , 1987, The Journal of biological chemistry.

[29]  E. Wimmer,et al.  Highly sensitive, fluorescent transformation marker for Drosophila transgenesis , 2000, Development Genes and Evolution.

[30]  T. Hamamoto,et al.  Mouse beta-galactoside alpha 2,3-sialyltransferases: comparison of in vitro substrate specificities and tissue specific expression. , 1997, Glycobiology.

[31]  J. Hollister,et al.  Engineering the protein N-glycosylation pathway in insect cells for production of biantennary, complex N-glycans. , 2002, Biochemistry.

[32]  A. Handler,et al.  piggyBac internal sequences are necessary for efficient transformation of target genomes , 2005, Insect molecular biology.

[33]  M. Bownes,et al.  Drosophila: A practical approach: edited by D. B. Roberts IRL Press, 1986. £26.00/$47.00 (xix + 295 pages) ISBN 0 94746 66 7 , 1987 .

[34]  Jared J. Aumiller,et al.  A transgenic insect cell line engineered to produce CMP-sialic acid and sialylated glycoproteins. , 2003, Glycobiology.

[35]  M. Summers,et al.  Transposon-mediated mutagenesis of a baculovirus. , 1985, Virology.

[36]  M. Summers,et al.  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 , 1983, Journal of virology.

[37]  J. Squire,et al.  The human UDP‐N‐Acetylglucosamine:α‐6‐d‐Mannoside‐β‐1,2‐N‐Acetylglucosaminyltransferase II Gene (MGAT2) , 1995 .

[38]  H. G. Wang,et al.  Assay for movement of Lepidopteran transposon IFP2 in insect cells using a baculovirus genome as a target DNA. , 1995, Virology.

[39]  A. Handler,et al.  The lepidopteran transposon vector, piggyBac, mediates germ-line transformation in the Mediterranean fruit fly. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[40]  A. Handler,et al.  Use of the piggyBac transposon for germ-line transformation of insects. , 2002, Insect biochemistry and molecular biology.