The nuclear body, POD, has been identified as the oncogenic target in acute promyelocytic leukemia. It is known that the chromosomal translocation between the PML and RARa gene occurs in this disease and the cellular distribution of PML is changed. In both the patient and the cellular model, treatment with retinoic acid results in reformation of the POD and remission in the patient. In order to obtain a better understanding of the POD and its unknown function, we wish to follow the dynamic recreation of this nuclear body in situ. To perform this study, a fusion between the PML and GFP proteins will be used to track the PML in the living cell. Secondly, optical trapping will be used to both assist in the microinjection of this marker into a suspension model cell line and also to trap the cell during visualization of this dynamic process.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
2P41RR001192-19
Application #
6280324
Study Section
Project Start
1998-05-15
Project End
1999-03-31
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
19
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of California Irvine
Department
Type
DUNS #
161202122
City
Irvine
State
CA
Country
United States
Zip Code
92697
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