Cookies on this website
We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.

Study co-led by Professor KJ Patel uncovers new mechanism for DNA repair that may help protect DNA from cancer-causing rearrangements

Champagne glasses with bubbles in the shape of DNA double helix

Alcohol consumption can indirectly cause damage to our DNA and elevate cancer risk. KJ Patel’s group in the MRC Laboratory of Molecular Biology’s (LMB’s) Protein and Nucleic Acid Chemistry (PNAC) Division, in a close collaboration with Puck Knipscheer’s group at the Hubrecht Institute in Utrecht, has identified a novel repair mechanism for DNA damage created by by-products of alcohol metabolism. Professor Patel will be moving to take up the Directorship of the MRC Weatherall Institute of Molecular Medicine (MRC WIMM) and the MRC Molecular Haematology Unit (MRC MHU) as announced last week.

DNA crosslinks are a very toxic form of DNA damage that block a cell’s ability to copy its DNA or transcribe it in order to produce proteins. This type of DNA damage is known to be caused by cisplatin, an important chemotherapy drug, and aldehydes, including acetaldehyde, a by-product of alcohol breakdown in our bodies. Professor Patel’s group had previously found that the Fanconi Anaemia (FA) DNA repair pathway fixes the DNA crosslinks formed by aldehydes.

In this study, the team wanted to investigate how the rules for repair differ between acetaldehyde-derived and cisplatin-derived crosslinks. To do this, Michael Hodskinson and his colleagues in Professor Patel’s group worked with Jason Chin’s group, also in the LMB’s PNAC Division, to devise a chemical method to make a single acetaldehyde crosslink in a short circular DNA molecule. Although these crosslinks could form in just a few seconds in a cell, it took the better part of 3 years to make them in a test tube.

Collaborating with Puck Knipscheer, who is an expert in creating cell-free DNA copying extracts, the team then incubated the synthetic circular DNA in frog egg extracts that have been primed to activate DNA copying and was able to study how a single crosslink was repaired. As expected, they saw rapid activation of the FA DNA repair pathway, leading to cutting out of the crosslink. However, they also made a surprising discovery.

Comparison of the two DNA repair pathways© MRC Laboratory of Molecular BiologyComparison of the two DNA repair pathways

A significant number of acetaldehyde crosslinks were repaired by a new pathway that did not need to excise the DNA crosslink and did not create a break in the DNA strand. More detailed experiments suggested that this new repair mechanism breaks the crosslink from within the DNA helix. The new pathway, however, cannot fix DNA crosslinks made by cisplatin, which must be repaired by the FA pathway. “

Perhaps the sole reliance on the FA DNA repair pathway for crosslinks caused by chemotherapeutic drugs might explain why they can so efficiently kill cancer cells - Professor Patel

Future work aims to determine the factors that carry out this new DNA repair pathway, and to determine its physiological importance. “This new research underscores that DNA crosslink repair, which is vital for our wellbeing, is only just beginning to be understood,” says Michael.

The work was funded by the MRC, Dutch Cancer Society, Netherlands Organisation for Scientific Research, Uehara Memorial Foundation, Mochida Memorial Foundation for Medical and Pharmaceutical Research, Wellcome Trust, Cancer Research UK, the European Research Council and a Japan Society for the Promotion of Science Postdoctoral Fellowship for Research Abroad.

 

Read the full paper.

Adapted from article originally published on the MRC LMB website.

Similar stories

Spin-out company Alethiomics launches

The enterprise will focus on developing targeted therapies for a specific family of blood cancers.

Study links the onset of circulation to changes in metabolism affecting blood stem cell development

A new paper published in Cell Reports by the de Bruijn Group indicates that the onset of circulation triggers a metabolic switch associated with the maturation of haematopoietic stem cells.

Interview with Excellence Award winner Dr Susan Shapiro

A member of the Oxford Centre For Haematology, Dr Shapiro, was recently interviewed by the Royal College of Pathologists.

Mohsin Badat receives ASH-BSH Abstract Achievement Award

Dr Mohsin Badat, a Clinical Training Research Fellow from the Higgs and Davies Groups has been awarded the ASH-BSH Abstract Achievement Award by the American Society of Haematology and the British Society of Haematology.

Iron integral to the development of life on Earth – and the possibility of life on other planets

A collaboration between researchers at the MRC WIMM and Department of Earth Sciences uncovers the importance of iron for the development of complex life on Earth.

Strong cytotoxic T cell responses to an internal viral component are associated with mild COVID-19 disease

Study from the Dong Group reveals key differences in the adaptive immune responses of patients with mild vs. severe COVID-19, highlighting a potential new vaccine target.