The bifunctional dihydrofolate reductase thymidylate synthase ofTetrahymena thermophilaprovides a tool for molecular and biotechnology applications

✍ Scribed by Lutz Herrmann; Ulrike Bockau; Arno Tiedtke; Marcus WW Hartmann; Thomas Weide

• Publisher: BioMed Central
• Year: 2006
• Tongue: English
• Weight: 646 KB
• Volume: 6
• Category: Article
• ISSN: 1472-6750
• DOI: 10.1186/1472-6750-6-21

✦ Synopsis

Background

Dihydrofolate reductase (DHFR) and thymidylate synthase (TS) are crucial enzymes in DNA synthesis. In alveolata both enzymes are expressed as one bifunctional enzyme.

Results

Loss of this essential enzyme activities after successful allelic assortment of knock out alleles yields an auxotrophic marker in ciliates. Here the cloning, characterisation and functional analysis of Tetrahymena thermophila's DHFR-TS is presented. A first aspect of the presented work relates to destruction of DHFR-TS enzyme function in an alveolate thereby causing an auxotrophy for thymidine. A second aspect is to knock in an expression cassette encoding for a foreign gene with subsequent expression of the target protein.

Conclusion

This system avoids the use of antibiotics or other drugs and therefore is of high interest for biotechnological applications.