The long term objective of this work is to develop a molecular understanding of the process by which centrosomes organize microtubules. The spatial orientation of microtubules is crucial for their function and is controlled by the centrosome. The centrosome has been recalcitrant to investigation so the basis for its function and regulation are unknown. We have discovered a highly conserved centrosome protein called pericentrin that is essential for cell division and organization of the microtubule cytoskeleton. Pericentrin provides us with a unique opportunity to understand centrosome function at the molecular level. A recent advance in our laboratory suggests that we will be able to identify and reconstitute the components of nucleation. We are now in an excellent position to: 1. Test the hypothesis that pericentrin is involved in centrosome assembly and define the sequence requirements for function. 2. Test the hypothesis that pericentrin assembles onto centrosomes in a cell cycle-specific phosphorylation-dependent manner. 3. Test the hypothesis that pericentrin binding proteins are involved in microtuble nucleation. Significant progress has been made toward th goals of this proposal. We have raised antibodies that block pericentrin function, produced mutant and wild type pericentrin cDNAs and fusion proteins and developed a novel in vitro assay for reconstituting centrosome function. Since that first submission of this proposal, we identified a pericentrin binding partner, perturbed centrosome structure using mutant pericentrin, and made the remarkable observation that pericentrin antibody-beads promote assembly of microtubules. These recent advances, molecular tools, and assays will allow us to make rapid progress in understanding the properties and function of pericentrin and centrosomes in general. Understanding centrosome function is important for several reasons. As the organizer of the microtubule cytoskeleton, the centrosome is a pivotal player in many fundamental cellular processes. Given its importance in the assembly of the mitotic spindle during cell division, the centrosome is a potential regulator of cell growth and a coordinator of morphogenesis. Centrosome- mediated microtubule polarity is critical for organizing the cytoplasm for intracellular vesicular transport and positioning of organelles. Despite its central position at the focus of microtubules and its central role in the life of a cell, the centrosome is poorly understood. Our preliminary results suggest that pericentrin will allow us to make important contributions in an area of biology that has been difficult to study. We are especially excited about the future prospect of realizing our long term goal of reconstituting centrosome function in vitro from individual components.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM051994-03
Application #
2459600
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1995-08-01
Project End
2000-07-31
Budget Start
1997-08-01
Budget End
1998-07-31
Support Year
3
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of Massachusetts Medical School Worcester
Department
Other Basic Sciences
Type
Schools of Medicine
DUNS #
660735098
City
Worcester
State
MA
Country
United States
Zip Code
01655
Hung, Hui-Fang; Hehnly, Heidi; Doxsey, Stephen (2016) The Mother Centriole Appendage Protein Cenexin Modulates Lumen Formation through Spindle Orientation. Curr Biol 26:793-801
Vertii, Anastassiia; Bright, Alison; Delaval, Benedicte et al. (2015) New frontiers: discovering cilia-independent functions of cilia proteins. EMBO Rep 16:1275-87
Vertii, Anastassiia; Zimmerman, Wendy; Ivshina, Maria et al. (2015) Centrosome-intrinsic mechanisms modulate centrosome integrity during fever. Mol Biol Cell 26:3451-63
Hung, Hui-Fang; Hehnly, Heidi; Doxsey, Stephen (2015) Methods to analyze novel liaisons between endosomes and centrosomes. Methods Cell Biol 130:47-58
de Souza, Edmarcia Elisa; Hehnly, Heidi; Perez, Arina Marina et al. (2015) Human Nek7-interactor RGS2 is required for mitotic spindle organization. Cell Cycle 14:656-67
Hehnly, Heidi; Doxsey, Stephen (2014) Rab11 endosomes contribute to mitotic spindle organization and orientation. Dev Cell 28:497-507
Chen, Chun-Ting; Hehnly, Heidi; Yu, Qing et al. (2014) A unique set of centrosome proteins requires pericentrin for spindle-pole localization and spindle orientation. Curr Biol 24:2327-2334
Chen, Chun-Ting; Ettinger, Andreas W; Huttner, Wieland B et al. (2013) Resurrecting remnants: the lives of post-mitotic midbodies. Trends Cell Biol 23:118-28
Chen, Chun-Ting; Hehnly, Heidi; Doxsey, Stephen J (2012) Orchestrating vesicle transport, ESCRTs and kinase surveillance during abscission. Nat Rev Mol Cell Biol 13:483-8
Hehnly, Heidi; Chen, Chun-Ting; Powers, Christine M et al. (2012) The centrosome regulates the Rab11- dependent recycling endosome pathway at appendages of the mother centriole. Curr Biol 22:1944-50

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