We have been investigating genes in Drosophila melanogaster that are required for accurate chromosome segregation during mitosis. Mutations in three of the genes we are studying result in the appearance of highly polyploid cells sometimes containing hundreds of chromosomes. Polyploid anaphase figures are observed, suggesting that the products of these genes function in a post-anaphase event we believe to be cytokinesis. The genomic regions containing all three genes have been cloned; we propose to continue these investigations so as to identify and to sequence the proper transcriptional units, and to generate antibodies against the corresponding gene products for future immunolocalization studies. A strong effort will be made to advance our understanding of the role of a fourth gene, l(1)zw10, mutations in which cause aneuploidy in a large proportion of cells in many types of mitotic tissues. Our cytological characterization of mutants suggests that the l(1)zw10 protein is required for proper sister chromatid separation at anaphase onset. We have further shown that the intracellular location of the protein encoded by l(1)zw10 undergoes several remarkable transitions in the course of the cell cycle. In particular, it resides on or near kinetochore microtubules at metaphase, but is then rapidly redistributed to the kinetochores at the beginning of anaphase. The experiments outlined in this proposal are designed to explore possible function of the l(1)zw10 product. We will ask whether this protein is required for any chromosome movements to the metaphase plate, determine whether it participates in the system rendering anaphase onset dependent on spindle integrity, and further investigate puzzling aspects of the phenotype that may provide clues about its functional role. We also intend to study the structures in which the protein is found at the ultrastructural level, and to determine how the novel intracellular distributions of the protein to these structures are achieved. Examination of the effects of other mitotic and meiotic mutations on the localization of the l(1)zw10 antigen may illuminate gene interactions required both for the localization pattern as well as other aspects of chromosome segregation. Finally, by exploiting the reagents we have generated, other components of the important mitotic organelles in which the l(1)zw10 product reside will be identified.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM048430-01
Application #
3307884
Study Section
Genetics Study Section (GEN)
Project Start
1992-09-30
Project End
1996-08-31
Budget Start
1992-09-30
Budget End
1993-08-31
Support Year
1
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Cornell University
Department
Type
Schools of Arts and Sciences
DUNS #
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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