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- Reader in Molecular Genetics of Hearing Loss
- The Ear Institute
- Faculty of Brain Sciences
People often ask “Is a disease or condition caused by nature or nurture?” – in fact a lot of the most common diseases are caused by a combination of these two things. I have always been interested in how an individual’s genes and their environment combine to cause disease and this is one of the things I am studying in hearing loss. I did my PhD in cardiovascular genetics where I learnt about how to study the genetics of complex diseases. When I left I spent some time studying the role a group of genes in the nervous system and by chance one of them turned out to be important in hearing. That’s the kind of thing that can happen in research – you suddenly get taken in a completely new direction.
It was actually quite timely because I was ready to move back into an area of research which was more clinically relevant and was also keen to set up my own group. Here at the UCL Ear Institute it is quite unusual in that there are lots of people working on the same disease but from different points of view which can be very challenging but the building we’re in (Centre for Auditory Research) facilitates interdisciplinary learning by forcing interactions between groups.
This has already proven to be successful –I now have a collaboration with Jonathan Gale’s group and we run some joint research projects together. We’ve also got an interaction with clinicians at the hospital next door which is beneficial for us in terms of getting patient samples and also encouraging clinicians to become more involved in research.
2: Survival mechanisms in hair cells (in collaboration with Jonathan Gale's Group). One of the reasons that the causes of age related hearing loss remain unclear is that we know very little about the molecular pathways of the hair cell. It is loss of the hair cell which is the precipitating cause of hearing loss. The inner ear is frequently subjected to potentially damaging environmental insults such as excessive noise. How the sensory receptor hair cells respond to such stimuli determines whether an insult is pathogenic or is successfully repaired. Deciphering the molecular mechanisms involved in these responses is therefore a pre-requisite to developing interventions to halt or reverse the damage. We have used a subtractive hybridisation strategy to identify a pool of genes whose expression is altered by two hair cell survival factors, Brn-3c and Barhl-1. As part of a collaboration with Dr Jonathan Gale (also at CAR), testing is underway to characterise the role of genes selected from this pool in protecting hair cells from damage and to decipher molecular survival pathways. The aim of our research is to: 1) identify the mechanisms which protect and maintain hair cell function; 2) develop subtractive hybridisation strategy was then used to identify a pool of genes whose strategies to improve the survival of hair cells; 3) test the efficacy of these in protecting against damage.
3. Investigating the Causes of Otosclerosis. Otosclerosis is a common form of hearing loss caused by dysregulation of the stapes bone in the middle ear. In a joint project with Prof Shak Saeed, surgeon at the Royal Nose, Throat and Ear Hospital we are examining the cause of the dysregulation in stapes bone removed from patients and performing a genetic analysis to identify the underlying cause of this disorder.
Keywords: Ageing, Genetics, Gene expression, Hearing, Hearing and balance
Conditions: Auditory system disorders, Deafness
Methods: Gene expression profiling - single cell , Gene expression profiling - tissue level, Genetically encoded reporters/indicators, Genetic screens, Genomic analyses
|1992||PhD||Doctor of Philosophy – Genetics||University of London|
|1985||BSc Hons||Bachelor of Science (Honours) – Biological Sciences||University of East Anglia|