Evaluating the impact of genotoxic aldehyde stress in premature ageing


   Department of Chemistry

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  Dr R Hopkinson, Dr Kayako Tanaka  No more applications being accepted  Competition Funded PhD Project (Students Worldwide)

About the Project

Aldehydes are highly reactive chemicals that are common pollutants and human metabolites. However, the vast majority of aldehydes’ biological functions are unknown. 

We believe that endogenous aldehydes are key regulators of human biology. Given their chemical reactivity, it is likely that aldehydes can affect multiple biochemical pathways by reacting with DNA and proteins. However, it is currently unclear what reactions occur in human cells and how these reactions affect human biology at the molecular and systems levels. 

Recent pioneering work has revealed a potential function for aldehydes in human ageing. These studies using mouse models suggest a link between genotoxic aldehyde stress and the p53 response, leading to early cell senescence. This is a hallmark of premature ageing (Wang et al., Mol. Cell, 2023). While these findings are extremely exciting, there is currently little known about the underpinning molecular mechanism. Identifying this mechanism is essential as it would redefine our understanding of human ageing and could lead to the development of anti-ageing therapies. 

Defining how aldehydes induce cell senescence requires the development of a simple and robust cell model where (i) cellular aldehyde levels can be easily modulated and quantified, and (ii) where the molecular mechanisms underpinning senescence, e.g. p53-dependent pathways, can be analysed in a sensitive and controlled manner. This project therefore aims to establish such a cell model and to use it to discover how aldehydes affect ageing-related biology. 

Objective 1: To establish human cell lines where endogenous aldehyde levels can be manipulated.  

The project will generate cell models deficient in aldehyde metabolism. These cells will be immortalised but ‘normal’ cells (unlike normally used cancer-derived cells), which will make them ideal for studying senescence-related biological pathways in healthy models without inducing senescence. Derivatives of these cells will also be generated with single and double knock-outs of ADH5 and ALDH2, which are key aldehyde-metabolising enzymes. This will enable us to test how aldehyde metabolism affects ageing. 

Objective 2: To develop methods to modulate and quantify cellular aldehyde levels. 

The project will develop methods to both deliver aldehydes to cells and to quantify cellular aldehyde levels in response to aldehyde exposure and to knock-out of aldehyde metabolism enzymes. This work will build on existing research in the Hopkinson group with formaldehyde-releasing small molecules and formaldehyde detection methods. The releasers and detection methods will ultimately be used in cell assays (see below).  

Objective 3: To study the effects of aldehydes on ageing-related cell functions  

The project will determine the aldehyde sensitivity and aldehyde metabolism efficiency of the cell models using reported cytotoxicity assays and NMR studies on cell lysates. The project will also study the effects of aldehydes and aldehyde releasers (see above) on cell cycle progression and p53-dependent biological pathways. These studies will include analysis of p53 levels and downstream markers of p53 induction. Any changes will be correlated with aldehyde levels using the aldehyde quantification methods. The status of DNA damage will also be assessed, while late work will test whether combinatorial exposure to aldehyde releasers and p53 modulators induces any synergistic effects. Overall, these studies will give unprecedented insight into the role of aldehyde in p53 biology and ageing.  

Techniques that will be undertaken during the project

·        CRISPR-Cas9-mediated gene editing 

·        Cell culture 

·        Organic synthesis 

·        Spectroscopic techniques, most notably NMR spectroscopy and mass spectrometry 

·        Western blotting 

·        Cell cycle analysis, including flow cytometry 

·        Indirect fluorescence microscopy 

Enquiries

Project Enquiries to [Email Address Removed]

Programme enquiries to [Email Address Removed]

To apply please refer to

https://le.ac.uk/study/research-degrees/funded-opportunities/bbsrc-mibtp


Biological Sciences (4) Chemistry (6)

Funding Notes

All MIBTP students will be provided with a 4 year studentship.
This includes:
Tuition fees at the UK fee rate*
a tax free stipend which for 2023/4 is £18,622 (2024/25 stipend to be confirmed)
a travel allowance in year 1
a travel/conference budget
a generous consumables budget
use of a laptop for the duration of the programme.
The University of Leicester will provide full overseas fee waivers for the duration of their study to all international students accepted at Leicester. The funder, UKRI, allows us to appoint up to 30% overseas students.
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