Overview
Explore the impact of cross-talk between the nuclear and mitochondrial genomes and identify genetic associations using hepatic transmitochondrial cybrids. You’ll develop an innovative knowledge of this axis to reveal the potential regulatory role of the mitochondrial genome upon hepatic function.
About this opportunity
It is widely known that differences in the nuclear genome contribute to aspects of us as individuals, from hair colour to lifespan. However, less well-known is that we all have a second source of DNA called mitochondrial DNA (mtDNA). mtDNA is only inherited from our mothers and is much smaller, coding only 13 genes involved in producing cellular energy. However, research has shown that changes in mtDNA can have profound effects not only on how we produce energy but also in phenotypic responses to ageing, disease and organ function.
Research has begun to identify nuclear DNA factors that have a critical role in hepatic function, but the potential role of mtDNA variation has not been considered. In part, this is due to two major limitations. Firstly, it has not been possible to study the effect of mitochondrial variation against a common nuclear background. Secondly, most population studies are grossly underpowered when considering mitochondrial variation. In this studentship, you will circumvent these longstanding limitations using an innovative approach. Specifically, your project will combine a novel cell-based technology, in the form of an in vitro model that enables the effects of distinct mitochondrial genotypes to be studied against a constant nuclear background. You will also learn how to calculate and apply a polygenic risk score specifically for mtDNA, called the mtDNA variant load model (mtVLM). Critically this project will be used to further develop this model. Thus, you will gain skills in two trending domains of current research, bioinformatics and genetic modelling alongside utilising molecular biology to define fundamental mechanisms.
It is the overall aim of this studentship to define hepatic pathways that are under the influence of mtDNA, to explore the impact of any cross-talk between the nuclear and mitochondrial genomes and to identify potential genetic associations. To do this you will use hepatic transmitochondrial cybrids. This research in this studentship will provide a novel understanding of this overlooked, potential regulatory, axis with likely implications for understanding an individual’s susceptibility to liver disease as well as its subsequent treatment.
You’ll receive training across a diverse range of computational and laboratory skills with which to undertake pioneering translational, functional genetic studies. They will be trained to use cutting-edge technology and complex data analysis, with advanced systems biology to build the mtVLM computational model.
The successful student will be trained in techniques including advanced cell biology transmitochondrial cybrid generation, molecular biology, proteomics, lipidomics and a suite of functional analyses. This rich dataset will then be used as the source for subsequent computational studies to develop and validate the mtVLM to reveal the potential regulatory role of the mitochondrial genome upon hepatic function.