Transgenic worms are commonly used in C. elegans research. Described is a simple, yet effective, protocol to introduce transgenes into worms using biolistic bombardment with DNA-coated gold particles. The effort involved and results of bombardment compare favorably with microinjection for the generation of transgenic animals.
The number of laboratories using the free living nematode C. elegans is rapidly growing. The popularity of this biological model is attributed to a rapid generation time and short life span, easy and inexpensive maintenance, fully sequenced genome, and array of RNAi resources and mutant animals. Additionally, analysis of the C. elegans genome revealed a great similarity between worms and higher vertebrates, which suggests that research in worms could be an important adjunct to studies performed in whole mice or cultured cells. A powerful and important part of worm research is the ability to use transgenic animals to study gene localization and function. Transgenic animals can be created either via microinjection of the worm germline or through the use of biolistic bombardment. Bombardment is a newer technique and is less familiar to a number of labs. Here we describe a simple protocol to generate transgenic worms by biolistic bombardment with gold particles using the Bio-Rad PDS-1000 system. Compared with DNA microinjection into hermaphrodite germline, this protocol has the advantage of not requiring special skills from the operator with regards to identifying worm anatomy or performing microinjection. Further multiple transgenic lines are usually obtained from a single bombardment. Also in contrast to microinjection, biolistic bombardment produces transgenic animals with both extrachromosomal arrays and integrated transgenes. The ability to obtain integrated transgenic lines can avoid the use of mutagenic protocols to integrate foreign DNA. In conclusion, biolistic bombardment can be an attractive method for the generation of transgenic animals, especially for investigators not interested in investing the time and effort needed to become skilled at microinjection.
Biolistic bombardment is a simple method to introduce foreign DNA into many organisms, including C. elegans 1,5,6,7,16. It relies upon gold particles forming a complex with DNA in the presence of CaCl2. Cationic polyamines, such as spermidine, protect DNA from nuclease degradation in vivo. Since spermidine is a labile molecule, it is important to store it in small aliquots at -20°C, and make the solution right before performing the bombardment. As we described in the bombardment protoco…
The authors have nothing to disclose.
This work was supported by seed funds from the University of Pittsburgh and NIH grant AG028977 to A.L.F.
Material Name | Tipo | Company | Catalogue Number | Comment |
---|---|---|---|---|
Gold particles | Inbio gold | BD021 | 1micron | |
Midiprep kit | Qiagen | 12143 | ||
Spermidine | Sigma | S4139 | ||
Protamine | Sigma | P4505 | ||
Macrocarriers | Biorad | 165-2335 | ||
PDS-1000/He Hepta System | Biorad | 165-2257 | ||
Rupture disk | Biorad | 165-2330 | ||
Nystatin | Sigma | N1638 | ||
Streptomycin | MP | 100556 |