This subproject is one of many research subprojects utilizing theresources provided by a Center grant funded by NIH/NCRR. The subproject andinvestigator (PI) may have received primary funding from another NIH source,and thus could be represented in other CRISP entries. The institution listed isfor the Center, which is not necessarily the institution for the investigator.Kinetochores function as the primary chromosomal attachment sites for spindle microtubules and play a central role in chromosome segregation. S. cerevisiae is an ideal model in which to study kinetochore assembly due to its 125 base pair sequence-specific centromere. To date, over 60 budding yeast kinetochore proteins have been identified, many of which are conserved in higher organisms. Nevertheless, it is not clear how these proteins function to ensure kinetochore-spindle attachment. Extracts from wild-type or mutant yeast strains will be used to determine sequence attachment specificity.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR011823-12
Application #
7602213
Study Section
Special Emphasis Panel (ZRG1-CB-H (40))
Project Start
2007-09-01
Project End
2008-08-31
Budget Start
2007-09-01
Budget End
2008-08-31
Support Year
12
Fiscal Year
2007
Total Cost
$768
Indirect Cost
Name
University of Washington
Department
Biochemistry
Type
Schools of Medicine
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
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