Unravelling The Genetic Cause Of Premature Ovarian Insufficiency
- Research Opportunity
- Royal Children’s Hospital/Murdoch Childrens Research Institute
|Professor Andrew Sinclairfirstname.lastname@example.org||+61383416322||Personal web page|
|Doctor Elena Tuckeremail@example.com||+61393454357|
Premature Ovarian Insufficiency (POI), affecting as many as 1 in 100 women, is a form of female infertility characterised by lack of menstruation and menopausal hormone levels before the age of 40. In some cases, young girls fail to get periods altogether and learn they have this menopause-like condition in early adolescence. POI not only interferes with a woman's reproductive potential, but is also associated with an increased risk of osteoporosis, mental health problems, cardiovascular disease, and earlier death.
Ample evidence indicates the genetic basis of POI, however, its genetic cause is complex with implicated genes having roles in various cellular processes. The majority of cases remain unexplained, limiting appropriate treatment and management of affected individuals.
We have DNA from the largest described cohort of women with POI (N>100), and we are using the latest genomic technologies to identify novel causes of the condition. In this project, you will mine sequencing data for pathogenic gene variants and perform experimental validation to prove causality. This will involve techniques such as western blotting, gene expression assays, qRT-PCR and immunofluorescence staining in control and patient cell lines. This project has already revealed some exciting new candidate genes involved in POI.
Your project will contribute to better treatment and counselling of affected individuals, as well as enabling the identification of family members before symptoms arise. This can allow early intervention such as cryopreservation of eggs and hormone-replacement therapy to minimise co-morbidities. Discovering new "disease genes" improves understanding of the process of ovarian biology, which can then enable the development of therapeutics which are largely lacking for this condition.
Faculty Research Themes
School Research Themes
Students who are interested in joining this project will need to consider their elegibility as well as other requirements before contacting the supervisor of this research
For further information about this research, please contact a supervisor.
Research NodeRoyal Children’s Hospital/Murdoch Childrens Research Institute
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