A low-cost apparatus for transforming Drosophila and detecting green fluorescent protein (GFP) genetic markers

Abstract

We describe the transformation of white mutant Drosophila simulans with a piggyBac transposon vector and a green fluorescent marker (GFP) and show how to construct inexpensive micro-manipulation and epifluorescence equipment for use in transposon-mediated germ-line transformation. Although the number of G0 adult flies (16) obtained in relation to the number of injected eggs was very low (12.5%) it was comparable to the proportion described by other authors and can be considered as a good rate of transformation.

transgenic Drosophila; piggyBac; GFP; transposable elements


ANIMAL GENETICS

SHORT COMMUNICATION

A low-cost apparatus for transforming Drosophila and detecting green fluorescent protein (GFP) genetic markers

Maríndia DepráI; Lenira Maria Nunes SepelII; Élgion Lucio da Silva LoretoII

IUniversidade Federal do Rio Grande do Sul, PPG Genética e Biologia Molecular, Porto Alegre, RS, Brazil

IIUniversidade Federal de Santa Maria, Departamento de Biologia, Santa Maria, RS, Brazil

Correspondence

ABSTRACT

We describe the transformation of white mutant Drosophila simulans with a piggyBac transposon vector and a green fluorescent marker (GFP) and show how to construct inexpensive micro-manipulation and epifluorescence equipment for use in transposon-mediated germ-line transformation. Although the number of G0 adult flies (16) obtained in relation to the number of injected eggs was very low (12.5%) it was comparable to the proportion described by other authors and can be considered as a good rate of transformation.

Key words: transgenic Drosophila, piggyBac, GFP, transposable elements.

Introduction

Transposon-mediated germ-line transformations have been the approach most extensively used to obtain transgenic insects and other animals (Handler, 2001). In this approach a DNA transposon is used in a binary vector/helper system that allows the precise and stable insertion of any desirable DNA sequence into the target genome. Although P-element transformation has been a routine technique for Drosophila researchers for more than twenty years (Rubin and Spradling, 1982), transposon-mediated germ-line transformations were restricted to this model organism because the P transposon is inactive in non-drosophilids (Rio and Rubin, 1988). More recently, this methodology has been extended to other insects (Klinakis et al., 2000; Handler, 2001), fish (Fadool et al., 1998) and chickens (Shermann et al., 1998) due to the use of vectors containing various other transposons (e.g. mariner, hermes, minos and piggyBac) which are functional in a wide range of animals and require no additional cofactors for mobilization (Horn and Wimmer, 2000).

Until a few years ago, another obstacle to the use of transposon-mediated germ-line transformation was the difficulty in obtaining marker genes that permit easier and more reliable identification of transgenic animals. In general, a species-specific transformation marker can be generated by isolating visible mutations in the species of interest, cloning the corresponding gene and rescuing the mutant phenotype by the incorporation of a wild copy of this gene by transformation. However, this process is very laborious for many species and often delays the development of new procedures. A universal marker that can be used to show gene transfer in any species is the green fluorescent protein (GFP) under the control of artificial promoters, this marker now being widely used in various species (Berghammer et al., 1999; Horn and Wimmer, 2000; Horn et al., 2000; 2002).

An additional restriction to the wide use of transposon-mediated germ-line transformation is the need for a micro-manipulator, micro-needles, micro-injection systems and, when the GFP marker is employed, a stereomicroscope equipped for epifluorescence. In this note we describe the transformation of Drosophila simulans with a GFP marker and show how to construct inexpensive micro-manipulation and epifluorescence equipment.

Material and Methods

Flies and the preparation of embryos

The white mutant strain (Torres, 2001) of Drosophila simulans was used as recipient for the marker. About 200 adult flies were transferred to a 300 mL empty bottle which was inverted over a petri dish containing banana medium consisting of 20% (w/v) banana, 1.5% (w/v) agar and sufficient food coloring to facilitate picking up of the eggs. After 30 min this first plate was removed and discarded because many of the embryos were old and partially developed at the time of laying, the bottle being placed on a second plate of the same medium for a further 30 min to allow the flies to deposit fresh embryos. Fine-tipped forceps were used to dechorionated the embryos by rolling them on double-sided adhesive tape before transferring them to a slide where they were lightly fixed onto double-sided adhesive tape and desiccated over CaCl2 for 2-5 min. To protect the eggs being from complete desiccation we covered them with halocarbon oil 700 (Sigma), Nujol mineral oil (liquid paraffin oil, available locally from pharmacies) also being tested as a cheaper alternative to halocarbon oil. After desiccation, the slide and embryos were transferred to a microscope for micro-injection by the method of Fujioka et al. (2000).

Plasmids

We used the pBac [3xp3-EGFPafm] (Horn and Wimmer, 2000) plasmid, containing the piggyBac transposon inverted terminal repeats (ITRs) and the GFP gene marker under the control of an artificial promoter containing three Pax-6 homo-dimer binding sites. This promoter drives strong expression of the GFP protein in the eye-tissues of larva, pupa and adult flies. The piggyBac transposase helper-plasmid used was the pBDSac helper-plasmid with its 5' terminus deleted (Handler and Harrell, 1999).

Another plasmid set was used to investigate possible GFP toxicity in D. simulans, this set consisting of a P element pCASPER construct, containing the mini-white gene along with the pp25.5 plasmid containing the P element transposase gene (Karess and Rubin, 1984). All the plasmids were prepared using the PEG protocol (Fujioka et al., 2000).

Injection procedure

To inject the DNA the embryos were lined up on slides and a micro-manipulator used to place a needle precisely at the posterior of the embryo. During injection, embryos need to be pushed against the needle, and it is better to do this by moving the microscope stage rather than the micro-manipulator controls. Since not all laboratories have access to a micro-manipulator we designed a micro-manipulation apparatus that uses the mechanical stage control of an old microscope. In our apparatus the stage verniers, control screws, slide holder and retaining clip are fixed onto a plate attached to a Leitz stereo-microscope lamp-support in such a way that the plate can move vertically and horizontally, this plate serving as a support for the embryo-injection needle (Figure 1).

We tested several different micro-injection systems employing micropipettes and syringes of various volumes attached to polyethylene tubes filled with paraffin oil, water or air and found that the simplest and most efficient system consisted of a 20 mL glass syringe attached to an intravenous injection 'butterfly' tube with a yellow micro-pipette tip glued to its free end to serve as a needle-holder (Figure 1). Needles were made from 0.2 mm internal diameter capillary tubes (Hyalo-technique laboratory, Chemistry Department, Federal University of Santa Maria, Santa Maria-RS, Brazil) by hand-pulling these capillaries over the flame of an alcohol lamp to produce capillaries so thin that they were invisible to the naked eye, a microscope being used to visualize the capillaries in order to break them with a shape scalpel and form fine needle-ends. The finest needles were glued with cyanoacrylic instant adhesive (SuperBonder®) onto a 10 mL micro-pipette tip, this arrangement allowing faster and easier needle replacement.

This apparatus was used to inject the embryos with ultra-pure water to which had been added 200 ng/mL of each vector and helper plasmid.

Epifluorescence microscopy

The excitation wavelength of GFP is between 480 ± 40 nm, detection of GFP normally requiring a microscope fitted with expensive high-voltage epifluorescence equipment. In our experiments we tested two different light sources, one consisting of inexpensive violet light-emitting diodes (LEDs, obtainable from electronic component stores) fed with a cheap power supply (Dove, 2002) and the other made from laser diodes (405 nm, 5 mW maximum output). For both systems we used a 510 nm emission band-pass filter attached to the objective lens of a Zeiss stereo-microscope (Figure 1-B). The observations were done in a darkroom with the operator wearing UV-blocking safety glasses.

Results and Discussion

Our results show that it was indeed possible to transform flies with GFP using the low-cost micro-injection and epifluorescence equipment described above. Although the number of adult flies obtained in relation to the number of injected eggs was low (Table1), it was comparable to the proportion previously described by Horn et al. (2000 and 2002).

Transformation frequency is normally reported as the percentage of transformed flies in relation to fertile adults in the G0 generation. Working with various insects, Handler (2002) reported piggyBac transformation frequencies ranging from about 1-2% to more than 40% for fertile G0 members. We found two transformed flies out of a total of 16 G0 adult flies (12.5%), which can be considered a good rate of transformation.

Felts et al. (2000) and Handler (2002) reported that GFP expression can be toxic to some insects, which may account for the low production of larvae and G0 flies with the GFP construct as compared to larvae and G0 flies containing the mini-white plasmid construct (Table 1).

Transformed flies were not obtained with the pCASPER construct (a P element combined with a mini-white gene), which may have been due to the fact that only a few eggs were injected with this combination and that the P element is not so efficient at transforming D. simulans (Kimura and Kidwell 1994).

Although mineral oil is cheaper and easier to obtain, halocarbon oil appeared to be more effective than mineral oil at protecting eggs from desiccation, in one case six times more larvae being obtained using halocarbon oil (Table 1).

Although LEDs permitted separation of transformed flies from untransformed flies the quality of the images was not as high as when laser diodes were used, laser diodes being highly efficient at producing good visualization of fluorescent eyes (Figure 2) and justifying the extra cost involved in purchasing these diodes.

In the near future more and more transposon-mediated germ-line transformations will be used to obtain transgenic insects and other animals for both academic and applied research. In this note we have described some procedures that permit laboratories that do not have the resources to buy commercial micro-manipulators and epifluorescence equipment to use transposon-mediated germ-line transformation technology in their research programs.

Acknowledgments

This work was supported by grants from FAPERGS (numbers 01/0927.4 and 00513957) and FIPE-UFSM (number 10100). We thank ISBiothec Ltda (Porto Alegre, RS) for providing laser diodes and filters, Dr.Tarso Kist (Department of Biophisics -UFRGS) for help regarding the fluorescence detection systems, Dr. Neri Paniz (Hyalo-technique laboratory, UFSM) for providing the capillaries. The pBac plasmid and pBDSac helper-plasmid were kindly provided by Dr. Ernest Wimmer (Universität Bayreuth, Germany).

Editor: Louis Bernard Claczko

Received: April 24, 2003; Accepted: October 12, 2003

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Publication Dates

  • Publication in this collection
    13 Apr 2004
  • Date of issue
    2004

History

  • Accepted
    12 Dec 2003
  • Received
    24 Apr 2003
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