Centromeres of eukaryotic chromosomes are specific regions along the chromatin fiber that play a fundamental role in chromosome movement. Centromere DNA sequences isolated from the yeast, Saccharomyces cerevisiae, enable foreign DNA introduced into yeast to function as ordinary yeast chromosomes during cell division. We will examine how the centromere DNA sequence interacts with chromatin components in the cell nucleus, including histone and non-histone proteins. We have been able to selectively excise the centromere from yeast cells and affinity purify the protein-DNA complex. This methodology provides a unique opportunity to identify proteins bound to centromere DNA in vivo. we will examine how the kinetochore components are assembled onto the DNA, and when the complex attaches to the mitotic apparatus. The ability to conditionally regulate centromere function by transcription from an adjacent promoter allows the precise genetic control of chromosome movement during the cell cycle. We will study when in the cell cycle chromosomes are subject to mitotic forces and how the cell monitors the fidelity of chromosome segregation. The conditional centromere and selected point mutations in centromere DNA are indistinguishable in their loss of function, but differ in the mechanism of inactivation. We can discriminate loss of protein binding at the centromere from mutations in protein-protein interactions required for centromere function, and will identify mutants in protein binding to centromere DNA. The identification of trans-acting factors required for chromosome movement will enable us to determine how these factors interact with the centromere DNA to give rise to a functional unit responsible for chromosome locomotion. We will determine the role of a tightly centromere-linked gene, SP015 in spindle morphogenesis. SP015 is a member of a new class of GTP-binding proteins, that are microtubule-based mechanochemical enzymes. Knowledge of the factors that control the organization of the centromere and spindle may provide fundamental principles governing the molecular mechanism of cell division.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM032238-11
Application #
3280884
Study Section
Molecular Biology Study Section (MBY)
Project Start
1983-07-01
Project End
1995-06-30
Budget Start
1993-07-01
Budget End
1994-06-30
Support Year
11
Fiscal Year
1993
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
Schools of Arts and Sciences
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Lawrimore, Josh; Doshi, Ayush; Friedman, Brandon et al. (2018) Geometric partitioning of cohesin and condensin is a consequence of chromatin loops. Mol Biol Cell 29:2737-2750
Suzuki, Aussie; Gupta, Amitabha; Long, Sarah K et al. (2018) A Kinesin-5, Cin8, Recruits Protein Phosphatase 1 to Kinetochores and Regulates Chromosome Segregation. Curr Biol 28:2697-2704.e3
Salmon, Edward D; Bloom, Kerry (2017) Tension sensors reveal how the kinetochore shares its load. Bioessays 39:
Tsabar, Michael; Haase, Julian; Harrison, Benjamin et al. (2016) A Cohesin-Based Partitioning Mechanism Revealed upon Transcriptional Inactivation of Centromere. PLoS Genet 12:e1006021
Suzuki, Aussie; Badger, Benjamin L; Haase, Julian et al. (2016) How the kinetochore couples microtubule force and centromere stretch to move chromosomes. Nat Cell Biol 18:382-92
Lawrimore, Josh; Aicher, Joseph K; Hahn, Patrick et al. (2016) ChromoShake: a chromosome dynamics simulator reveals that chromatin loops stiffen centromeric chromatin. Mol Biol Cell 27:153-66
Ohkuni, Kentaro; Takahashi, Yoshimitsu; Fulp, Alyona et al. (2016) SUMO-Targeted Ubiquitin Ligase (STUbL) Slx5 regulates proteolysis of centromeric histone H3 variant Cse4 and prevents its mislocalization to euchromatin. Mol Biol Cell :
Lawrimore, Josh; Vasquez, Paula A; Falvo, Michael R et al. (2015) DNA loops generate intracentromere tension in mitosis. J Cell Biol 210:553-64
Verdaasdonk, Jolien S; Stephens, Andrew D; Haase, Julian et al. (2014) Bending the rules: widefield microscopy and the Abbe limit of resolution. J Cell Physiol 229:132-8
Stephens, Andrew D; Quammen, Cory W; Chang, Binny et al. (2013) The spatial segregation of pericentric cohesin and condensin in the mitotic spindle. Mol Biol Cell 24:3909-19

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