Each cytoplasmic organelle of a eukaryotic cell must divide and segregate into the daugther cells during the cell division cycle. We propose biochemical, cytological, and genetic approaches to illuminate the mechanisms of this process, using the vacuole (lysosome) of yeast as a model. We have observed that even the smallest yeast bud contains a single small vacuole, and that the vacuole grows in size as the bud grows. The parent cell vacuole does not grow during the cell cycle. These observations suggest a highly regulated mechanism of vacuole growth in the bud. Through the proposed studies, we hope to understand how organelle division is achieved, how it is regulated by the cell cycle, and how organelles can interact with the cytoskeleton to achieve orderly spatial segregation.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM038895-02
Application #
3295639
Study Section
Molecular Cytology Study Section (CTY)
Project Start
1987-07-01
Project End
1992-06-30
Budget Start
1988-07-01
Budget End
1989-06-30
Support Year
2
Fiscal Year
1988
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
Schools of Medicine
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Tsai, Chia-Lun; Rowntree, Rebecca K; Cohen, Dena E et al. (2008) Higher order chromatin structure at the X-inactivation center via looping DNA. Dev Biol 319:416-25
Rowntree, Rebecca K; Lee, Jeannie T (2006) Mapping of DNA replication origins to noncoding genes of the X-inactivation center. Mol Cell Biol 26:3707-17
Weisman, L S; Emr, S D; Wickner, W T (1990) Mutants of Saccharomyces cerevisiae that block intervacuole vesicular traffic and vacuole division and segregation. Proc Natl Acad Sci U S A 87:1076-80