The aims of this proposal are to define how human MAD2 (hsMAD2) functions as a mitotic checkpoint gene and to determine if disruption of hsMAD2 contributes to the generation of neoplasia in mouse models. hsMAD2 is the human homolog of a mitotic checkpoint gene first identified in budding yeast (scMAD2). The investigator proposes to test the hypothesis is that the biochemical mechanism underlying human MAD2 checkpoint function is its ability to inhibit the APC through its interactions with Cdc16 and Cdc27. In addition, MAD2 will be disrupted in both ES cells and mice to determine the contribution made by MAD2 to mitotic checkpoint control in mammalian cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
3R01GM054601-03S1
Application #
6232321
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Program Officer
Zatz, Marion M
Project Start
1997-05-01
Project End
2001-04-30
Budget Start
2000-05-01
Budget End
2001-04-30
Support Year
3
Fiscal Year
2000
Total Cost
$60,838
Indirect Cost
Name
Sloan-Kettering Institute for Cancer Research
Department
Type
DUNS #
064931884
City
New York
State
NY
Country
United States
Zip Code
10065
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