Genomic instability, the hallmark of human cancer, can involve activating mutations at oncogene loci, the accumulation of tumor suppressor mutations and specific chromosome losses that uncover tumor suppressor deficiencies. Cell cycle checkpoint, roritriols guard against such genome alterations. Indeed, high fidelity chromosome replication and transmission depend on elaborate mechanics that must be precisely controlled in the cell cycle context The S-phase checkpoint is a mechanism that establishes a dependence relationship between the biochemically unrelated cellular processes of DNA replication and mitotic cell division. A functional S-phase checkpoint ensures that genome duplication and segregation occur without error and this checkpoint is therefore a critical signaling pathway that guards against genome instability. Understanding S-phase checkpoint control is an important goal to increase our knowledge of cancer etiology. In the clinic, checkpoint integrity of tumor cells is highly relevant for designing effective treatment regimes, since compromised checkpoint controls affect the sensitivity of cells to therapeutic agents. This application seeks to understand the functions of novel S-phase checkpoint components. In addition, we propose to specifically investigate a novel Late S-phase Checkpoint pathway that we recently identified. Some, but not all, of the late S-phase checkpoint components are known. We will therefore investigate the functions of known S-phase checkpoint proteins and screen for currently unknown factors. These factors will inevitably be critical for the maintenance of genome stability and will be conserved in humans.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA099033-05
Application #
7238552
Study Section
Special Emphasis Panel (ZCA1-SRRB-3 (O1))
Program Officer
Pelroy, Richard
Project Start
2003-06-01
Project End
2009-05-31
Budget Start
2007-06-01
Budget End
2009-05-31
Support Year
5
Fiscal Year
2007
Total Cost
$308,855
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Genetics
Type
Schools of Medicine
DUNS #
555917996
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Lane, Andrew B; Giménez-Abián, Juan F; Clarke, Duncan J (2013) A novel chromatin tether domain controls topoisomerase II? dynamics and mitotic chromosome formation. J Cell Biol 203:471-86
Hsu, W-S; Erickson, S L; Tsai, H-J et al. (2011) S-phase cyclin-dependent kinases promote sister chromatid cohesion in budding yeast. Mol Cell Biol 31:2470-83
Gimenez-Abian, Juan F; Clarke, Duncan J (2009) Cytological analysis of chromosome structural defects that result from topoisomerase II dysfunction. Methods Mol Biol 582:189-207
Diaz-Martinez, Laura A; Gimenez-Abian, Juan F; Clarke, Duncan J (2008) Chromosome cohesion - rings, knots, orcs and fellowship. J Cell Sci 121:2107-14
Vas, Amit Cj; Clarke, Duncan J (2008) Aurora B kinases restrict chromosome decondensation to telophase of mitosis. Cell Cycle 7:293-6
Clarke, Duncan J; Bachant, Jeff (2008) Kinetochore structure and spindle assembly checkpoint signaling in the budding yeast, Saccharomyces cerevisiae. Front Biosci 13:6787-819
Vas, Amit C J; Andrews, Catherine A; Kirkland Matesky, Kathryn et al. (2007) In vivo analysis of chromosome condensation in Saccharomyces cerevisiae. Mol Biol Cell 18:557-68
Diaz-Martinez, Laura A; Gimenez-Abian, Juan F; Clarke, Duncan J (2007) Cohesin is dispensable for centromere cohesion in human cells. PLoS One 2:e318
Diaz-Martinez, Laura A; Gimenez-Abian, Juan F; Clarke, Duncan J (2007) Regulation of centromeric cohesion by sororin independently of the APC/C. Cell Cycle 6:714-24
Clarke, Duncan J; Vas, Amit C; Andrews, Catherine A et al. (2006) Topoisomerase II checkpoints: universal mechanisms that regulate mitosis. Cell Cycle 5:1925-8

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