Going Fishing in the Protein Pond Using Histones as Bait
The choice between the repair mechanisms is made at the molecule BARD1. Image credit: Helmholtz Zentrum München
When DNA in the cell nucleus gets damaged, our cells can resort to a variety of repair mechanisms. A recent study published in 'Nature Cell Biology', elucidates the molecular basis by which a cell makes the choice between these repair mechanisms.
The trick the scientists used: they developed a molecular bait to fish out the relevant proteins from the cell nucleus. According to the authors, this study opens up new possibilities for cancer therapies in the future.
The sequence of base pairs in the DNA contains the genetic information of all living things. Not all genes, however, are active at the same time – this also depends on other factors that are happening around the DNA. Histones play a major role in this. "Histones are proteins around which our DNA is wrapped and which thus serve to package the genetic material," says corresponding author Dr. Till Bartke, deputy director of the Institute of Functional Epigenetics (IFE) at Helmholtz Zentrum München. "Depending on how the histones are chemically modified, they can have different effects on the DNA and control gene activity”. The primary aim of Bartke and the IFE is to find out how this so-called 'histone code' works.
To achieve this, the researchers reconstruct known chemical histone modifications in a test tube and investigate which proteins selectively bind to them in an extract made from the nuclei of cells. "Put simply, we build a molecular bait with defined histones and use it to go fishing in the nucleus – and then it gets exciting to see what we will have on our ‘hook’," says Bartke.
DNA repair in focus
In their current research work, Bartke and his team used this method to search for proteins that bind specifically to newly formed chromatin*. "The idea was to identify proteins that are able to differentiate between old and new chromatin and that therefore have a function in the replication and repair of DNA," says the molecular biologist. The researchers found a group of structurally related enzyme complexes that are involved in the cell's choice of DNA repair pathway.** In further investigations, Danish colleagues led by Anja Groth at the Biotech Research and Innovation Centre (BRIC) of the University of Copenhagen elucidated in detail which proteins and structural elements participate in the cell's decision which of the different DNA repair mechanisms to initiate.
Approach for cancer treatment?
The key element in this repair process is an enzyme complex associated with BRCA1 (abbreviation for 'Breast Cancer 1'), a gene which has received considerable attention as a risk marker for breast cancer.*** "Carriers of mutations in the BRCA1 gene have an increased risk of developing breast or ovarian cancer because their DNA damage repair system is faulty, and this in consequence can lead to an accumulation of further harmful mutations. However, cancer patients who carry mutations in the BRCA1 gene can be treated with PARP inhibitors, a class of drugs that are particularly effective in these patients," says Bartke.
As part of the publication, British scientists led by Ross Chapman at the Wellcome Centre for Human Genetics in Oxford then specifically investigated the effects of mutations in the BRCA1 complex, focusing on the part responsible for the recognition of the newly formed chromatin. Cells in which this region was inactivated could be killed very effectively by a PARP inhibitor.
"Due to the collaboration of our three research groups, we now know the exact function of these important DNA repair proteins, and with the chromatin binding site of the BRCA1 complex we have already identified a target structure that we can use for medical intervention in order to treat cancer patients. Using small molecules, it would for example be possible to imitate the BRCA1 mutation and thereby make PARP inhibitors usable for a broader spectrum of patients that do not carry this mutation." A promising start has been made, says Bartke, and companies are already developing such molecules.
* Whereas in old chromatin the lysine in position 20 of histone H4 (H4K20) is almost always modified with two methyl groups (H4K20me2), the chromatin that is newly formed during DNA synthesis is characterized by (still) no methyl groups being present at this position (H4K20me0). By comparing these two states and the proteins bound to them, Bartke and his team were able to identify protein complexes that specifically recognize newly formed chromatin (H4K20me0) and therefore must have a function in the replication and repair of the genetic material.
** In the 'non-homologous end joining' pathway two non-homologous ends of the DNA are joined together if there is no sister chromatid available that can serve as a template. This method is very error-prone and as a result leads to mutations in the genome. Homologous recombination, on the other hand, repairs DNA damage using the intact genetic information on the sister chromatid and is considered to be virtually error-free.
*** The actress Angelina Jolie, for example, underwent a precautionary breast amputation because she carries an inherited mutation in the BRCA1 gene.
This article has been republished from materials provided by the German Research Center for Environmental Health. Note: material may have been edited for length and content. For further information, please contact the cited source.
Nakamura, K., Saredi, G., Becker, J. R., Foster, B. M., Nguyen, N. V., Beyer, T. E., . . . Groth, A. (2019). H4K20me0 recognition by BRCA1–BARD1 directs homologous recombination to sister chromatids. Nature Cell Biology. doi:10.1038/s41556-019-0282-9