Award details

Stochastic modelling chromosome replication

Reference	BB/G001596/1
Principal Investigator / Supervisor	Professor Conrad Nieduszynski
Co-Investigators / Co-Supervisors	Dr Alessandro De Moura
Institution	University of Nottingham
Department	Sch of Biology
Funding type	Research
Value (£)	542,585
Status	Completed
Type	Research Grant
Start date	01/03/2009
End date	31/05/2012
Duration	39 months

Abstract

Complete, accurate genome replication is essential for life. DNA replication is controlled by regulating the activation of replication origins - the sites of initiation of bi-directional replication forks. Eukaryotic genomes have an excess of potential replication origin sites, only a subset of which are utilised in any given cell cycle. The presence of more potential origins than are actually used may provide genome replication with robustness to ensure complete replication within S phase, particularly in the face of insults such as DNA damage. The purpose of this research is to develop and validate a predictive mathematical model of chromosome replication, and to use this model to understand how robustness to replication impediments is ensured to allow successful genome replication. Mathematical models of biological processes require the definition and measurement of the parameters that define the system. Budding yeast chromosome replication is particularly amenable to modelling, since the system is well characterised and amenable to whole genome methods for measuring the system parameters. Moreover, the genome structure can be genetically manipulated to test predictions. We have developed a preliminary mathematical model of chromosome replication. Next we will experimentally validate this model by testing its ability to predict the replication dynamics of perturbed replication systems. For example, we will use modified yeast strains in which individual replication origins have been deleted. Then we will extend the model to simulate the response of the replication system to insults, such as DNA damage, to uncover how genome replication retains robustness. In the long term, determining these mechanisms will be crucial for understanding the biological basis of genetic diseases, including cancer, and improving therapeutic strategies.

Summary

All cells contain a complete copy of the organism's DNA, the genetic blueprint of life, packaged into discrete units called chromosomes. Since new cells need a copy of the genetic material, the chromosomes must be completely and accurately replicated before the cell can divide. Eukaryotes, such as yeast and humans, have large genomes with millions of bases encoding the genetic information. To ensure complete replication of these genomes within the allowed time, the process of DNA replication starts at multiple sites along each chromosome, called replication origins. These replication origins are specialised DNA sequences that assemble the cellular machinery that then moves along the DNA reading and copying the genetic material. It is essential that the cell activates sufficient replication origins to ensure complete replication of the chromosomes. The importance of controlling replication origin activation is highlighted by the genome instability that may result from uncontrolled chromosome replication. Despite the importance of DNA replication origins we understand little about the DNA sequences that specify and control them. Failures in the processes of DNA replication lead to genetic instability and diseases such as cancer and congenital disorders. We hope that a better understanding of the basic biology that ensures genetic integrity will give new insights that will allow improved diagnosis and treatment of these diseases. We want to understand how the multiple replication origins on each chromosome are coordinated to ensure that the chromosome is successfully replicated. To study this 'system' we have developed a mathematical model that can be used to simulate the behaviour of all the replication origins on a chromosome. Now we will use our mathematical model to make predictions about chromosome replication that we can test experimentally in the lab. This will allow us to improve the model and include more complex scenarios. One such scenario is what happenswhen the DNA replication process encounters damage to the DNA. This is important, as damage to the DNA gives rise to genetic diseases such as cancer. Furthermore, many drugs that target cancer cells (chemotherapy) work by damaging the DNA, since cancer cells are more vulnerable to DNA damage than normal healthy cells. By combining mathematical modelling and experimental work we aim to identify the strengths and weaknesses of the chromosome replication process that may underlie genetic diseases such as cancer. In the long-term this work will help in our understanding of the biological basis of genetic diseases, including cancer, and may lead to new therapeutic strategies.

Committee	Closed Committee - Engineering & Biological Systems (EBS)
Research Topics	Microbiology, Systems Biology
Research Priority	X – Research Priority information not available
Research Initiative	X - not in an Initiative
Funding Scheme	X – not Funded via a specific Funding Scheme

I accept the terms and conditions of use (opens in new window)

export PDF file

back to list new search