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Single-molecule analysis of double-stranded DNA break repair in living bacteria

ReferenceBB/S008012/1
Principal Investigator / Supervisor Professor Meriem El Karoui
Co-Investigators /
Co-Supervisors
Institution University of Edinburgh
DepartmentSch of Biological Sciences
Funding typeResearch
Value (£) 361,751
StatusCompleted
TypeResearch Grant
Start date 01/06/2019
End date 30/11/2022
Duration42 months

Abstract

Our objective is to study the in vivo mechanisms and kinetics of the repair of double-stranded DNA breaks (DSBs) inside living bacteria. In bacteria, DSBs are dealt with mainly via homologous recombination by proteins RecBCD and RecA: broken molecules are faithfully repaired by copying the missing information from another, intact, chromosome. RecBCD loads on a DSB, and starts unwinding and degrading it to help RecA form a filament that eventually finds homologous DNA, and catalyses strand exchange and DNA repair. RecBCD and RecA have been studied in vitro using biochemical and single-molecule approaches; however, such approaches cannot replicate the enormous complexity of the cellular cytoplasm, thus leaving severe gaps in our mechanistic understanding of DSB repair in cells. To address the outstanding questions, we formed a collaborative three-site team that will analyse DSB repair mechanisms at the single-molecule level in live Escherichia coli. We will use in vivo single-molecule tracking of expressed fluorescent proteins and internalised fluorescent DNA substrates in single living bacterial cells, along with sophisticated data analysis. After validating the necessary proteins and DNA, we will characterize the RecBCD search determinants in cells with different degree and types of DNA breaks (e.g., ones generated using fluoroquinolones). We will monitor the process of DNA-end location in real-time using simultaneous tracking of RecBCD and target DNA molecules. We will use in vivo single-molecule FRET to characterise how DNA ends are processed by the endonuclease and helicase activities of RecBCD; these studies will be guided by complementary in vitro experiments. Finally, we will monitor the formation of RecA filaments on synthetic RecBCD substrates (to be formed controllably in cells) and monitor the kinetics of homology search; these studies will also examine the presence of 1-D search along DNA as a mechanism that accelerates this DNA-repair pathway.

Summary

Our study uses ultra-sensitive microscopes to observe important processes taking place during the repair of DNA, the molecule wherein the genetic information is stored mainly in the form of chromosomes. DNA repair is the general term for the collection of the different ways living cells fix different types of damage to their genetic material. As such, DNA repair is central for the survival and growth of all living organisms. Specifically, our work focuses on the process of repairing broken chromosomes when they are exposed to breaks on both strands of the DNA double helix; such breaks are known as "double-stranded breaks". In bacteria, these DNA breaks are often fixed by two protein machines called RecBCD and RecA, that act in a well coordinated fashion. The RecBCD machine manages to find the broken DNA ends amongst huge amounts of intact DNA in the cell and removes part of the broken DNA end to leave a special DNA structure. This structure is then recognised by many copies of the RecA machine that forms of stiff DNA filament that embarks on a fascinating and mysterious search for an intact copy of the chromosome. This process needs to be fast and specific, since any errors not fixed in time can lead to dangerous mutations or even cell death. Much of what we know about how DNA breaks are fixed comes from studies with purified proteins and DNA in the test tube; these involve simple mixtures of the RecBCD and RecA machines with DNA sequences and helper proteins that accelerate or facilitate the process. However, the mechanisms of DNA repair in actual living organisms can be very different, due to the myriad of other biological components that are present in cells, and due to the way that the genes are packaged in the "bacterial nucleoid", which is a tightly packed structure made of the bacterial DNA and some of its proteins. To provide an example of the complexity that characterises DNA repair in living cells, one can consider the task of RecA: to search just 50 letters of DNA within the entire chromosome, which is a molecule longer than 5,000,000 letters and highly folded. Another example of the complexity has to do with other proteins that can interfere with or facilitate the function of RecBCD when it tries to fix DNA ends that have been formed by treating pathogenic bacteria with antibiotics. To study the process of DNA repair in its natural environment of living cells, we will use advanced fluorescence microscopy to look at how the RecBCD machine searches, finds, and helps broken DNA ends with the help of its partner RecA inside living bacterial cells. We will use the bacterium Escherichia coli, which is a simple model organism for understanding biological mechanisms. A special feature of our work is that it is performed using a special microscope (a "single-molecule fluorescence microscope"). This microscope is carefully designed to allow detection and monitoring of individual (single) fluorescent molecules inside living cells (as opposed to conventional microscopes that require thousands or millions of fluorescent molecules). Using our powerful microscope to record movies and track the position of the proteins as they move, we will see how proteins search and find different types of broken DNA ends, either on the chromosome or on synthetic types of broken DNA that allow us to see the process more directly and in real time. We will also study how individual RecBCD machines cut out the DNA end to prepare the ground for the landing of the RecA machines. Finally, we will study how RecA forms the type of DNA that is able to search for the correct copy of the DNA to fix the damaged part. Our studies will improve our understanding of how DNA repair works in living cells, and help other scientists to study DNA repair in other organisms (such as humans), as well as to develop new pharmaceuticals that will improve the health of humans, animals and plants by disabling the DNA repair machinery of dangerous microbes.

Impact Summary

The main proposal aim is to understand how bacteria repair their chromosomes; this aim has direct impact on understanding how bacteria become tolerant and resistant to clinically relevant antibiotics such as quinolones and trimethoprim. Our work will advance substantially our fundamental understanding of the mechanisms at play and develop cutting-edge techniques that elucidate the activity of these antibiotics in vivo. Moreover, our new technologies and assays will be applicable to identifying the mode-of-action of new potential antimicrobial lead compounds that target chromosomes and DNA-binding proteins in bacteria. Apart from the obvious academic impact, the project will have significant economic and social impact. Continuous engagement with our technology transfer offices and industrial partners will allow early identification of opportunities for translation of our scientific outputs. Economic impact will be maximized through skills development and commercialisation options. Skills development: The project will result in two highly trained PDRAs with a diverse and interdisciplinary set of skills, and experience of working at the interface between physical and biological sciences. Both PDRAs will gain skills in quantitative large-scale image processing (including machine-learning-based algorithms), an area with critical shortages of such skills in industry. Commercialisation: ANK is engaged in discussions with three clinicians at the Oxford John Radcliffe Hospital and industrial partner Oxford Nanoimaging to develop rapid antimicrobial susceptibility tests based on single-cell imaging. We expect that some mechanistic findings, electroporated DNA sensors, and imaging/data-analysis methods will be of interest for our clinical and industrial collaborators. MeK is actively discussing with Sanofi Infectious Diseases applying single-molecule tracking assays to the mode-of-action characterisation of several new antimicrobials. Understanding the mode-of-action for existing and new antibiotics is important for their optimal use and for developing new antibiotics based on rational design. Social impact. We will engage with the broader society and help stir enthusiasm for science via: Workshops: the MeK team will deliver 2 workshops in local schools using the innovative and highly successful Science Art Workshop (SAW) Trust approach to teaching science to children using the power of words and art. Videos: we will produce three 3-min videos for public engagement: one directed to the microscopy/instrumentation industry, one directed to microbiologists and clinicians, and one directed to high schools and general public. Website: we will create a project website that will address the three communities targeted with the three videos (industry, clinicians, general public). Science festivals: we will participate in our local Science festivals, with the Oxford Science Festival and the Edinburgh Science Festival being the main venues. The involvement will have sci-art entries, and/or practical demonstrations similar to the ones used in the SAW workshops. Media: to enhance public understanding of science, the PI, co-Is and PDRAs will make every effort to communicate the importance and implications of our work to the media via interviews, press releases and radio/TV appearances, social media networks, as well as through public lectures, discussions, science Open days and outreach events. Conference organisation. To maximise our impact, we will organise a conference to engage potential academic, clinical and commercial end-users. Specifically, we will organise "Single-Molecule Bacteriology 2020", a 3.5-day conference on single-molecule imaging in single bacteria. The workshop will familiarize clinicians and industrial attendees with the latest in single-molecule bacterial biology, and allow them to discuss clinical and industrial needs with academics, thus catalysing collaborations between academia, hospitals and industry.
Committee Research Committee C (Genes, development and STEM approaches to biology)
Research TopicsMicrobiology
Research PriorityX – Research Priority information not available
Research Initiative X - not in an Initiative
Funding SchemeX – not Funded via a specific Funding Scheme
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