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Open Access Research article

Reduction of gene repair by selenomethionine with the use of single-stranded oligonucleotides

Timothy R Schwartz and Eric B Kmiec*

Author Affiliations

Department of Biological Sciences, University of Delaware, Delaware Biotechnology Institute, 15 Innovation Way Newark, DE 19711, USA

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BMC Molecular Biology 2007, 8:7  doi:10.1186/1471-2199-8-7

Published: 26 January 2007

Abstract

Background

The repair of single base mutations in mammalian genes can be directed by single-stranded oligonucleotides in a process known as targeted gene repair. The mechanism of this reaction is currently being elucidated but likely involves a pairing step in which the oligonucleotide align in homologous register with its target sequence and a correction step in which the mutant base is replaced by endogenous repair pathways. This process is regulated by the activity of various factors and proteins that either elevate or depress the frequency at which gene repair takes place.

Results

In this report, we find that addition of selenomethionine reduces gene repair frequency in a dose-dependent fashion. A correlation between gene repair and altered cell cycle progression is observed. We also find that selenium induces expression of Ref-1 which, in turn, modifies the activity of p53 during the cell cycle.

Conclusion

We can conclude from the results that the suppression of gene repair by introduction of selenomethionine occurs through a p53-associated pathway. This result indicates that the successful application of gene repair for treatment of inherited disorders may be hampered by indirect activation of endogenous suppressor functions.