Mistakes in chromosome segregation during meiosis or mitosis can lead to spontaneous abortion or to abnormalities such as Down syndrome, They have also been implicated in the genetic progressions leading to cancer and aging. Our laboratory studies several genes in Drosophila that are required for proper chromosome segregation. We believe that this organism offers important advantages in genetics, genomics and cytology that provide unique opportunities to investigate chromosome behavior and cell cycle progression during cell division. We first focused on an evolutionarily conserved gene called zwlO. Mutations in zwlO not only disrupt chromosome segregation, but they also prevent the operation of the spindle assembly checkpoint that regulates anaphase onset. The ZW1O protein displays an unusual, dynamic pattern of localization during the cell cycle, moving between chromosomal kinetochores and kinetochore microtubules. We found that this pattern is influenced by bipolar tension across individual chromosomes. We also discovered that ZW1O is part of a large protein complex, one of whose activities is to target the molecular motor dynein to the kinetochore. The first specific aim describes further investigations on ZW1O.We will use real-time video microscopy to characterize the distribution of a ZW1O-GFP fusion protein during the cell cycle. We will determine which domains of ZW1O are required for various aspects of its intracellular distribution and function. We will analyze double mutant combinations to position ZW1O in the biochemical pathways underlying the spindle checkpoint and other aspects of anaphase onset. We will also test whether all aspects of the zw10 mutant phenotype, including its effects on the spindle checkpoint, are caused by the absence of dynein at the kinetochore. The second specific aim is to characterize biochemically and genetically the large complex of which ZW1O is a part. Preliminary efforts to purify the complex by affinity chromatography have been promising. We will use several techniques to verify the association of candidate proteins with ZW1O. We will then identify these proteins by mass spectrometry, and will determine whether they are subject to post-translational modification. Our ultimate goal is to obtain antibodies against these proteins, as well as mutations in the genes encoding them. The third specific aim will exploit our identification in the previous funding period of a set of new mutations that cause precocious sister chromatid separation, aneuploidy, or metaphase arrest in Drosophila. We will study the phenotypes associated with these mutations in more detail, clone selected mutant genes, and then investigate the intracellular location of the corresponding gene products. Because we are focusing on genes not previously known to function in any aspect of mitosis, we believe the genetic and antibody reagents obtained by the proposed studies will provide a broadened and unique view of the events occurring at anaphase onset.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM048430-12
Application #
6710143
Study Section
Genetics Study Section (GEN)
Program Officer
Carter, Anthony D
Project Start
1992-09-30
Project End
2005-03-31
Budget Start
2004-04-01
Budget End
2005-03-31
Support Year
12
Fiscal Year
2004
Total Cost
$373,198
Indirect Cost
Name
Cornell University
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
872612445
City
Ithaca
State
NY
Country
United States
Zip Code
14850
Filter, Joshua J; Williams, Byron C; Eto, Masumi et al. (2017) Unfair competition governs the interaction of pCPI-17 with myosin phosphatase (PP1-MYPT1). Elife 6:
Défachelles, Lénaïg; Raich, Natacha; Terracol, Régine et al. (2015) RZZ and Mad1 dynamics in Drosophila mitosis. Chromosome Res 23:333-42
Williams, Byron C; Filter, Joshua J; Blake-Hodek, Kristina A et al. (2014) Greatwall-phosphorylated Endosulfine is both an inhibitor and a substrate of PP2A-B55 heterotrimers. Elife 3:e01695
Wainman, Alan; Giansanti, Maria Grazia; Goldberg, Michael L et al. (2012) The Drosophila RZZ complex - roles in membrane trafficking and cytokinesis. J Cell Sci 125:4014-25
Blake-Hodek, Kristina A; Williams, Byron C; Zhao, Yong et al. (2012) Determinants for activation of the atypical AGC kinase Greatwall during M phase entry. Mol Cell Biol 32:1337-53
Kim, Min-Young; Bucciarelli, Elisabetta; Morton, Diane G et al. (2012) Bypassing the Greatwall-Endosulfine pathway: plasticity of a pivotal cell-cycle regulatory module in Drosophila melanogaster and Caenorhabditis elegans. Genetics 191:1181-97
Yamamoto, Tomomi M; Blake-Hodek, Kristina; Williams, Byron C et al. (2011) Regulation of Greatwall kinase during Xenopus oocyte maturation. Mol Biol Cell 22:2157-64
Goldberg, Michael L (2010) Greatwall kinase protects mitotic phosphosites from barbarian phosphatases. Proc Natl Acad Sci U S A 107:12409-10
Peng, Aimin; Yamamoto, Tomomi M; Goldberg, Michael L et al. (2010) A novel role for greatwall kinase in recovery from DNA damage. Cell Cycle 9:4364-9
Wainman, Alan; Creque, Jacklyn; Williams, Byron et al. (2009) Roles of the Drosophila NudE protein in kinetochore function and centrosome migration. J Cell Sci 122:1747-58

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