| Posted: August 19, 2008 |
Modified DNA helps scientists understand secrets of DNA repair mechanisms |
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(Nanowerk News) A modified DNA is helping scientists to understand the sophisticated DNA repair mechanisms that allow dormant bacteria to come 'back to life'.
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Thomas Carell and Eva Bürckstümmer at the Ludwig Maximilian University of Munich, Germany, have made short DNA strands containing lesions ("Synthesis and properties of DNA containing a spore photoproduct analog" – free access article). Carell explains that this is the key to understanding DNA repair. 'So far any study of this enigmatic process has been hampered by a lack of DNA containing this lesion,' he explains.
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The lesions are analogues of those triggered when UV light acts on DNA stored in spores such as the Bacillus bacteria spore. In nature, these spores can lie dormant for many years, storing DNA, but then return to life, explains Carell. How spores store DNA and how lesion repair occurs are the questions the German duo would like to answer.
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Carell and Bürckstümmer made their DNA strands by synthesising two isomers of a dinucleotide lesion analogue and incorporating them into DNA. They found that one DNA was more stable than the other, suggesting that the natural lesion could have a similar structure to the analogue in the more stable DNA. Carell points out that similar lesion analogues are substrates for the spore DNA repair enzyme so that the new strands could help further studies into the enzyme mechanism.
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Glen Burley, an expert in DNA nanotechnology at the University of Leicester, UK, says that the work is exciting because it provides a method for investigating how bacterial spores repair damaged DNA. 'This is a compelling question as DNA damage processes in spores differ from those in mammals,' he says. 'These methods would likely lead to a greater understanding of how spores can survive for long periods and in hostile conditions - for example hot springs or under UV light exposure.'
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Carell explains that although the repair process in the spore is unique, the phenomenon of lesion recognition by enzymes is more general. 'Such enzymes are also operating in our cells,' he says, 'so a deeper understanding of this class of enigmatic enzymes is desperately needed.' Carell adds that he is particularly interested in learning more about failures in the repair process. 'These are responsible for mutations which in turn lead to dangerous cellular situations which might produce cancer,' he says.
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