Project Details
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Studies on the mechanism of pathway choice during repair of ionizing radiation induced DNA double strand breaks

Subject Area Nuclear Medicine, Radiotherapy, Radiobiology
Term from 2019 to 2023
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 415585014
 
Final Report Year 2024

Final Report Abstract

Breaks in the DNA that cut the molecule in pieces are called DNA double strand breaks (DSBs) and are very dangerous for the cell because they are very difficult to repair correctly. DSBs are induced by x-rays and charged particles present in the environment on earth and in space, but are also induced by radiations used to diagnose diseases and to treat cancer. Cells have four ways to repair DSBs, but only one of them does a perfect job. The one that is actually very often used by the cell is fast but makes mistakes. So, the question arises how the cell decides what repair way to use. Some researchers think that the decision is random and depends upon what repair protein happens to be close to the break at the moment it is generated. Since we found this model intellectually unsatisfying, we searched in this project for alternative explanations and developed ways to test its validity experimentally. The project focused on a protein named KU that is a key component of the fast but erroneous way of DSB repair, and MRE11, which in many ways initiates the pathway that does the perfect job. In a set of biochemical and genetic experiments we provide evidence for interaction between the two proteins that guides a transition of the DSB from erroneous to processing. While a lot more work will be needed to demonstrate the validity and generate more details of the model in cells, the results generated pave the way for such research in the future. We anticipate that such research will help to develop means to protect people from the adverse effects of radiation and to improve the radiotherapy of cancer therapy.

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