PiggyBac FLEX Conditional Gene Expression Vector (Cre-Off)


The piggyBac FLEX conditional Cre-Off gene expression vector combines VectorBuilder’s highly efficient piggyBac vector system with the Cre-responsive FLEX conditional gene expression system to help you achieve transfection-mediated permanent integration of Cre-responsive FLEX switch into the host genome. The FLEX Cre-Off switch utilizes two pairs of LoxP-variant recombination sites flanking a gene of interest in an arrangement that facilitates robust inactivation of gene expression by Cre-dependent inversion of the coding sequence.

The FLEX Cre-Off switch consists of two pairs of heterotypic LoxP-variant recombination sites, namely LoxP having the wild-type sequence and Lox2272 having a mutated sequence, flanking an ORF. Both LoxP variants are recognized by Cre, but only identical pairs of LoxP sites can recombine with each other and not with any other variant. The LoxP and Lox2272 sites are organized in an alternating fashion, with an antiparallel orientation for each pair. In the absence of Cre recombinase, the ORF can be expressed under the control of the user-selected promoter. In the presence of Cre, the LoxP and Lox2272 sites undergo recombination with the other LoxP and Lox2272 sites respectively, resulting in the inversion of the ORF to an antisense orientation and excision of one from each pair of identical recombination sites. Inversion of the ORF prevents expression of the gene of interest. Since the ORF is now flanked by two different LoxP-variant sites, no further recombination events will take place even when Cre is present.

The piggyBac vector system is technically simple, utilizing transfection (rather than viral transduction) to permanently integrate your gene(s) of interest into the host genome. The piggyBac FLEX conditional Cre-OFF gene expression system comprises two components: the transposon plasmid and the transposase (helper PBase). The transposon plasmid contains two terminal repeats (TRs) bracketing the region to be transposed. The FLEX Cre-OFF switch described above is cloned into this region. The transposase can be delivered into target cells through two methods. A helper plasmid encoding PBase can be transiently transfected into cells. Alternatively, target cells can be injected with in vitro transcribed PBase mRNA. When the helper PBase and the piggyBac transposon vector are co-introduced into target cells, the transposase produced from the helper would recognize the two TRs on the transposon and insert the flanked FLEX Cre-OFF switch including the two TRs into the host genome. Insertion typically occurs at host chromosomal sites that contain the TTAA sequence, which is duplicated on the two flanks of the integrated fragment. Gene expression can then be inactivated in the presence of Cre recombinase upon Cre-mediated inversion of the coding sequence. Through both methods of delivering transposase, it is expressed for only a short time. Upon the loss of the helper plasmid or degradation of transposase mRNA, the integration of the transposon into the host genome becomes permanent.

PiggyBac is a class II transposon, meaning that it moves in a cut-and-paste manner, hopping from place to place without leaving copies behind. (In contrast, class I transposons move in a copy-and-paste manner.) If the transposase is reintroduced into the cells, the transposon could get excised from the genome of some cells, footprint-free.

While this vector system can be used in tissue culture cells, it is particularly suitable for the generation of transgenic animals. When a transgenic animal carrying such a vector is crossed with an animal carrying a tissue-specific Cre transgene, the gene of interest would be turned off in the progeny animals carrying both types of transgenes, specifically in cells where the tissue-specific Cre is expressed and the user-selected promoter driving the gene of interest is active.

For further information about this vector system, please refer to the papers below.

References Topic
Mol Cell Biochem. 354:301 (2011) Review on the piggyBac system
Cell. 122:473 (2005) Efficient transposition of the piggyBac (PB) transposon in mammalian cells and mice
Gene. 216:55 (1998) Characterization of LoxP mutants, including Lox2272
Nat Biotechnol. 21:562 (2003) Development of the FLEX switch system
J Neurosci. 28:7025 (2008) Application of a FLEX switch system


The piggyBac FLEX conditional Cre-Off gene expression vector is designed to achieve Cre-mediated conditional inhibition of gene expression in mammalian cells and animals. Expression of the gene of interest is initially under the control of the user-selected promoter and can be permanently silenced by co-expression of Cre recombinase, which will invert the gene of interest to its antisense orientation. 

This vector along with the helper plasmid encoding the piggyBac transposase are optimized for high copy number replication in E. coli, efficient transfection into a wide range of target cells, and high-level expression of the transgene carried on the vector.


Switch-like gene inactivation: Inversion of the user-selected ORF to its antisense orientation in the presence of Cre recombinase prevents any leaky gene expression.

Stable gene inactivation: Treatment with Cre recombinase will permanently invert the user selected ORF to its antisense orientation. Upon inversion of the ORF to its antisense orientation followed by excision of one from each pair of similar LoxP sites by recombination, the ORF will be flanked by two different LoxP-variant sites which will prevent further recombination events even when Cre is present. This will permanently prevent transcription of the gene of interest.

Permanent integration of vector DNA: Conventional transfection results in almost entirely transient delivery of DNA into host cells due to the loss of DNA over time. This problem is especially prominent in rapidly dividing cells. In contrast, transfection of mammalian cells with the piggyBac transposon plasmid along with the helper plasmid can deliver genes carried on the transposon permanently into host cells due to the integration of the transposon into the host genome.

Technical simplicity: Delivering plasmid vectors into cells by conventional transfection is technically straightforward, and far easier than virus-based vectors which require the packaging of live virus.

Very large cargo space: Our piggyBac FLEX conditional Cre-Off gene expression vector can accommodate ~30 kb of total DNA. The plasmid backbone, transposon-related sequences and the sequences necessary for Cre-mediated recombination only occupy about 3.1 kb, leaving plenty of room to accommodate the user's sequence of interest.


Limited cell type range: The delivery of piggyBac vectors into cells relies on transfection. The efficiency of transfection can vary greatly from cell type to cell type. Non-dividing cells are often more difficult to transfect than dividing cells, and primary cells are often harder to transfect than immortalized cell lines. Some important cell types, such as neurons and pancreatic β cells, are notoriously difficult to transfect. These issues limit the use of the piggyBac system.

Key components

5' ITR: 5' inverted terminal repeat. When a DNA sequence is flanked by two ITRs, the piggyBac transpose can recognize them, and insert the flanked region including the two ITRs into the host genome.

Promoter: The promoter driving your gene of interest is placed here.

Lox2272: Recombination site for Cre recombinase. Mutated Lox site with two base substitutions of wild type LoxP. Incompatible with LoxP sites. When Cre is present, the LoxP and LoxP2272 sites will be cut and recombine with compatible sites.

LoxP: Recombination site for Cre recombinase. Incompatible with Lox2272 sites. When Cre is present, the LoxP and Lox2272 sites will be cut and recombine with compatible sites.

ORF: The open reading frame of your gene of interest is placed here, in a sense orientation.

rBG pA:  Rabbit beta-globin polyadenylation signal. It facilitates transcriptional termination of the upstream ORF.

CMV promoter: Human cytomegalovirus immediate early promoter. It drives the ubiquitous expression of the downstream marker gene.

Marker: A drug selection gene (such as neomycin resistance), a visually detectable gene (such as EGFP), or a dual-reporter gene (such as EGFP/Neo). This allows cells transduced with the vector to be selected and/or visualized.

BGH pA: Bovine growth hormone polyadenylation signal. It facilitates transcriptional termination of the upstream ORF.

3' ITR: 3' inverted terminal repeat.

Ampicillin: Ampicillin resistance gene. It allows the plasmid to be maintained by ampicillin selection in E. coli.

pUC ori: pUC origin of replication. Plasmids carrying this origin exist in high copy numbers in E. coli.

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