- Research article
- Open Access
High-level gene expression in Aedes albopictus cells using a baculovirus Hr3 enhancer and IE1 trans activator
© Gray and Coates; licensee BioMed Central Ltd. 2004
- Received: 31 March 2004
- Accepted: 13 July 2004
- Published: 13 July 2004
Aedes aegypti is the key vector of both the Yellow Fever and Dengue Fever viruses throughout many parts of the world. Low and variable transgene expression levels due to position effect and position effect variegation are problematic to efforts to create transgenic laboratory strains refractory to these viruses. Transformation efficiencies are also less than optimal, likely due to failure to detect expression from all integrated transgenes and potentially due to limited expression of the transposase required for transgene integration.
Expression plasmids utilizing three heterologous promoters and three heterologous enhancers, in all possible combinations, were tested. The Hr3/IE1 enhancer-trans activator in combination with each of the constitutive heterologous promoters tested increased reporter gene expression significantly in transiently transfected Aedes albopictus C7-10 cells.
The addition of the Hr3 enhancer to expression cassettes and concomitant expression of the IE1 trans activator gene product is a potential method for increasing the level of transgene expression in insect systems. This mechanism could also potentially be used to increase the level of transiently-expressed transposase in order to increase the number of integration events in transposon-mediated transformation experiments.
- West Nile Virus
- Renilla Luciferase
- Luciferase Expression
- Klenow Fragment
- Hsp82 Promoter
Through the efforts of many individuals in the past few years, it has become possible to genetically transform a wide variety of non-drosophilid insects of medical and agricultural importance . The ability to genetically transform mosquito species allows researchers to better understand mechanisms of vector competence, design novel methods to disrupt vector-pathogen relationships and develop new insect control strategies [2–5]. New molecular methods could potentially augment continued traditional efforts to control malaria and other re-emerging arthropod-borne diseases. Similar approaches may also be used to stem the devastating infestation of economically important crops by insecticide-resistant pest strains.
Mosquitoes transmit to humans some of the most debilitating and deadly diseases known. According to the World Health Organization, malaria alone is responsible for one million deaths annually . Additionally, the transmission of yellow fever, dengue fever, West Nile virus and a variety of other encephalitis viruses permanently disrupt or end untold numbers of lives. Both anopheline [7–10] and culicine [11–17] mosquito species have been successfully transformed. In all cases, the process is labor-intensive with a few successful experiments yielding transformation efficiencies ranging from 0.5% to 13%. These transformation efficiencies are low compared to the nearly 50% previously reported in Drosophila with vectors up to 8 kb in size . Additionally, transgene expression in the yellow fever mosquito varies considerably both between and within families [11, 12, 19], likely due to differences in the transcriptional environments of specific insertion sites within the genome, such as the proximity of the transgene to enhancers or heterochromatic stretches of DNA. This phenomenon is of particular concern in the Ae. aegypti genome given its large size (~780 Mb) and its apparent pattern of short-period interspersion where single copy genes (1 to 2 kb) alternate with short (200–600 bp) or medium (1–4 kb) length repetitive sequences . The problem is complex, however transposition has been shown to be dependent upon the amount of transiently available transposase to catalyze vector integration [21, 22]. Also, the effective use of genetically-altered mosquitoes to augment current disease vector control requires the ability to create and maintain transgenic lines with consistent, predictable and high-level expression patterns of effector transgenes.
Looking to maximize the transcription of rare transgenes that do land in favorable environments and to potentially increase the levels of transiently available transposase, we tested the ability of three different enhancer elements; SV40 , copia ULR (Drosophila)  and Hr3 (Bombyx mori nuclear polyhedrosis virus or NPV) , to increase the levels of transcription from each of three heterologous promoters from the following genes: actin5C  and polyubiquitin (Ubi-p63E – hereafter referred to as pUb)  from Drosophila and the intermediate early gene (IE1)  from the Autographa californica multicapsid nuclear polyhedrosis virus (MNPV). Additionally, we tested the ability of the B. mori baculovirus IE1 gene product , which binds to repetitive sequences within the baculovirus homologous regions (Hrs) [30, 31] and has previously been shown to function as a powerful trans activator in transfected lepidopteran cells , to yet further increase gene expression in mosquito cells.
The Hr3 enhancer and the IE1 transactivator increase reporter gene activity in transiently transfected C7-10 Aedes albopictus cells
IE1 transactivator interacts with promoter sequences in addition to the Hr3 enhancer
Change in Basal Luciferase Expression from Promoters with Addition of the IE1 Trans activator
↑ 17 x
↑ 30 x
↓ 1.9 x
↑ 169 x
↑ 138 x
↑ 1.2 x
↑ 11 x
↑ 202 x
↓ 18.3 x
Unexpectedly, the internal control for transfection and protein recovery, Renilla luciferase, could not reliably be used as such in the presence of the trans activator. The data presented reveal a differential effect of the IE1 trans activator (Fig. 2 and Table 1) that profoundly affects expression levels from the two luciferase plasmids in an enhancer/promoter-dependent manner. This compromises the ability to compare expression values both within an experiment where IE1 is present in some samples but not in others and between experiments where different batches of cells and assay reagents are employed. The results of a single experiment involving the trans activator are reported here, however additional experiments show similar results. The ratio of firefly to Renilla luciferase is reported for all promoter/enhancer combinations to allow accurate comparison of the three promoters alone and in combination with each of the three enhancers. It should be noted that the addition of the transactivator does significantly increase firefly luciferase expression from all three promoters with the Hr3 enhancer sequence, though this is masked by the simultaneous increase in expression from the Renilla luciferase control plasmid.
The IE1 trans activator is clearly interacting with the promoters in trans, even in the absence of the Hr3 enhancer element (Fig. 2, Table 1 and data not shown). This observation agrees with previously published data that the cytoplasmic A3 actin gene promoter of B. mori was upregulated as much as one hundred-fold by the co-transfection of a plasmid encoding the B. mori IE1 gene product (BmIE1) . When the Hr3 enhancer is present, there is a cooperative effect, and luciferase expression increases as much as 200-fold (Fig. 1) over that of the promoter alone. This cooperativity is consistent with results obtained with Hr3-enhanced CAT expression cassettes driven by the B. mori cytoplasmic actin gene promoter co-expressed with the BmIE1 protein in lepidopteran cell lines Bm5 and Sf 21 (an increase of up to three orders of magnitude) .
The significant differences seen in expression from each of the promoters tested (Fig. 2 and Table 1) reveal that not all promoters are affected in the same manner, nor is the co-transfected plasmid. The presence of the Hr3 enhancer region upstream of the promoter driving expression of the IE1 trans activator protein, results in high levels of IE1 protein from a relatively low amount of plasmid DNA. Despite this abundance of IE1 protein, it appears that transcription from the pUb promoter, in the absence of the Hr3 enhancer, increases only 11-fold (Fig. 2A and Table 1), while transcription from the hsp82 promoter driving Renilla luciferase expression is exceptionally high (Fig. 2B and Table 1). The simplest explanation is that the IE1 protein has different affinities for binding sites on the various promoters and/or the IE1 protein is sequestering necessary basal transcription factors. It has also been observed that some viral promoters, IE-0, IE-2 and PE-38, are inhibited by IE1 expression [33–35]. Clearly, the actions of the IE1 trans activator in this study are consistent with its ability to bind Hrs [36–38]. In addition, the protein has two independent functional acidic activation domains and two potential positively-charged inhibitory domains [39, 40], consistent with its observed ability to both enhance and inhibit expression from different promoters. Also, lower concentrations of the plasmid bearing the IE1 gene sequence in these transient assays result in greater increases in luciferase expression (see additional file 2). This observation is consistent with the mechanism of negative regulation by the IE1 protein previously proposed  where the cooperative binding of the Hrs occurs at a lower concentration than that required for binding to the half sequence regions (Hs) present in negatively regulated promoters. It is also consistent with the presence of the Hr3 enhancer sequence on the plasmid producing the IE1 trans activating protein, which results in up-regulation of IE1 transcription, consequently reducing the number of plasmid copies needed to produce optimal protein levels. When this experiment was repeated using pUb to drive Renilla luciferase expression (data not shown and additional file 3), significant differences between promoters were also observed, though not the same differences described above with the hsp82-Renilla expression plasmid. Finally, it should be noted that each of the enhancers alone also differentially affected the expression from each promoter. These data collectively highlight the value of evaluating the effects of new promoter/enhancer/trans activator combinations on the expression of a reporter gene within a related cell line, prior to investing significant time and effort in the creation of transgenic lines. Though cell lines do not completely mimic the cellular and nuclear environment of an entire organism, they can yield significant insight into both the potential interaction between regulatory elements driving transgene expression and the potential impact of unknown endogenous trans acting factors.
Clearly, we have shown that the baculovirus homologous region, Hr3, along with the IE1 trans activating protein, significantly increases transgene expression from each of the three heterologous, constitutive promoters tested in mosquito cells. Some concern does exist that endogenous promoters might be down-regulated by the presence of the IE1 protein, and that available host cell transcription factors might be sequestered by complexes stabilized by the IE1 trans activator, however a lower concentration of IE1 trans activator would likely mitigate these effects. Preliminary transposition assays confirm the ability of the Hr3 enhancer/IE1 trans activator combination to function in syncytial preblastoderm mosquito embryos and to significantly increase observed transposition frequencies when used to drive transposase expression (Coates, et al., unpublished data). Use of tissue-specific promoters/enhancers and/or inducible expression may effectively reduce any potential fitness load imposed by interactions of the ie1 protein with endogenous regulatory elements. Perhaps the most promising application is the use of HR/IE1 in helper plasmids transiently expressing transposase in an attempt to increase the number of stable transgene integration events by increasing the amount of available transposase, particularly if germline-specific promoters were used to express the trans activator protein. The HR/IE1 strategy is a promising tool for high-level transgene expression and/or increased transposition frequency in culicine mosquitoes and possibly other insect species as well.
Construction of the luciferase expression plasmids
A 2.7-kb Hind III-Sal I fragment from pGL2-Basic (Promega), containing the firefly luciferase coding region and the SV40 poly-Adenylation signal, was inserted into the corresponding sites of pBCKS+ (Stratagene) to create pBCLuc. A 2.7-kb Sma I-Sal I fragment from pBCLuc was inserted into the Sma I-Sal I sites of pSLfa 1180fa ( to create pSLLuc. The Drosophila Actin5C promoter was excised from pHermesA5CEGFP  by Pst I and Bam HI digestion and inserted into the corresponding sites of PSLLuc to create PSLAct5CLuc. The Sac II site was removed from pIE1-3 (Novagen) and then the 657-bp Eco RI-Bam HI fragment containing the AcMNPV IE1 promoter was inserted into the corresponding sites of pSLLuc to create pSLIE1Luc. A 2-kb Kpn I-Bam HI fragment from pB [pUB-nls-EGFP]  containing the Drosophila polyubiquitin promoter was inserted into the corresponding sites of pSLLuc to create pSLpUbLuc. The copia ULR was amplified by polymerase chain reaction (PCR) from copia LTR-ULR-CAT  using the primers 5'-AAGCTTGGGCCCAGTCCATGCCTA-3' and 5'-CCGCGGATTACGTTTAGCCTTGTC-3', cleaved by digestion with Hind III and Sac II and inserted into the corresponding sites of pBCKS+ to create pBCcULR. The Hind III-Sac II fragment from this plasmid was then inserted into the corresponding sites of pSLAct5CLuc and pSLIE1Luc to create pSLcULRAct5CLuc and pSLcULRIE1Luc. pBCcULR was digested with Hind III and the site filled with the Klenow fragment of DNA polymerase I (Promega), then digested with Sac II and ligated into pSLpUbLuc which had been cut with Not I and the site filled with Klenow fragment, then cut with Sac II to create pSLcULRpUbLuc. The SV40 enhancer region from pRL-SV40 (Promega) was PCR-amplified using the primers 5'-AAGCTTCTGAGGCGGAAAGAACCA-3' and 5'-CCGCGGAAAATTAGCCAGCCATGG-3', digested with Hind III and Sac II and inserted into the corresponding sites of pBCKS+ to make pBCeSV40. The Hind III-Sac II fragment of pBCeSV40 was then inserted into the corresponding sites of pSLAct5CLuc and pSLIE1Luc to create pSLeSV40Act5CLuc and pSLeSV40IE1Luc. pBCeSV40 was digested with Hind III, the site filled with Klenow fragment, then digested with Sac II and ligated to pSLpUbLuc digested with Not I, the site filled with Klenow fragment and subsequently digested with Sac II to produce pSLeSV40pUbLuc. A 1.2-kb Pst I-Bam HI fragment containing the B. mori NPV Hr3 enhancer from p153  was inserted into the corresponding sites of pBCKS+ to create pBCHr3. The Pst I-Bam HI fragment of pBCHr3 was inserted into the corresponding sites of pSLAct5CLuc to create pSLHr3Act5CLuc. The Hind III-Sac II fragment of pBCHr3 was inserted into the corresponding sites of pSLIE1Luc to create pSLHr3IE1Luc. The Eco RV-Sac II fragment of pBCHr3 was ligated to pSLpUbLuc digested with Not I, the site filled with Klenow fragment, and then digested with Sac II to create pSLHr3pUbLuc. phsp82Renilla Luc was created by inserting a 1-kb Kpn I-Bam HI fragment from pKhsp82  into the corresponding sites of pBCKS+ and then inserting the Kpn I-Pst I fragment from this plasmid into the corresponding sites of pRL-SV40. ppUbRenilla Luc was created by first digesting pSLpUbLuc with Not I, filling in the site with Klenow fragment, then digesting with Pst I to produce a2-kb fragment which was ligated to pRL-SV40 prepared by digestion with Bgl II, the site filled with Klenow fragment and then digested with Pst I.
Cell cultures and transfections
Aedes albopictus C7-10 cells were maintained at 25°C with 5% CO2 in Eagle's media plus 5% fetal calf serum with the following additions per liter: 10 mL 10% (wt/vol) D(+)glucose, 10 mL 200 mM L-glutamine, 10 mL MEM vitamin solution, 20 mL MEM non-essential amino acids, 10 mL Penicillin/Streptomycin (10,000 U/mL), 29.3 mL sodium bicarbonate (7.5% w/v) . 400 μL of cells at a density of 2 × 10-6 cells/mL were seeded into 24-well microtiter plates and incubated at 25°C for 24 hrs. Cells were transfected with 0.4 μg total DNA and 0.8 μL LipofectAMINE 2000 (Life Technologies) in 10 μL serum-free, antibiotic-free media. phsp82Renilla Luc and the firefly constructs were transfected at a 1:2 ratio. The IE1 transactivator plasmid  was present as 1/10 of the total DNA.
Transfected cells were assayed 24 hrs. post-transfection using a Turner Designs 20/20 luminometer and a Dual Luciferase Assay (Promega). The manufacturer's passive lysis protocol was followed. In addition, cell lysates were snap frozen in liquid nitrogen immediately after lysis to minimize luciferase protein degradation. All samples were diluted 20-fold in 1 × PLB (passive lysis buffer) in order to obtain a reading within the range of the luminometer.
We would like to thank Dr. Ann Fallon for her gift of the C7-10 cell line, Dr. Kostas Iatrou for his gift of the plasmids containing the IE1 transactivator and the Hr3 enhancer, and Yong Zhou and Jeremy Haag for their technical assistance. We would also like to thank the anonymous reviewers for their valuable comments and insights. This work was supported by NIH Grant #RO1 AI46432 to C.J.C.
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