Ubiquitination and Fanconi Anemia
- Research Opportunity
- PhD, Masters by Research, Honours, Master of Biomedical Science
- Number of Honour Places Available
- Medicine and Radiology
- St Vincent's Institute of Medical Research
|Dr Andrew Deansfirstname.lastname@example.org||Personal web page|
Ubiquitin is a small protein that is covalently attached to proteins to alter their function. In the cancer predisposition disorder Fanconi anemia, defective FANCA some how causes the attachment of ubiquitin to FANCD2 to fail. This apparently simple defect results in phenotypes of bone marrow failure, developmental problems and increased rates of leukaemia and solid tumours.
We have developed a biochemical system to study this important ubiquitination reaction. This project aims to test the biochemical mechanism by which this ubiquitination occurs, and how FANCA protein works in the reaction. A combination of approaches using the latest technologies will also test how patient associated mutations in FANCA cause Fanconi Anaemia. This will be combined with cell-based assays investigating the mechanism by which defects in ubiquitination lead to leukaemia predisposition.
This project is conducted in St Vincent’s Institute of Medical Research, Genome Stability Unit.
Faculty Research Themes
School Research Themes
PhD, Masters by Research, Honours, Master of Biomedical Science
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 Group / Unit / Centre
Research NodeSt Vincent's Institute of Medical Research
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