Chromosome segregation is a complex process that requires the precisely coordinated action of many proteins. The interactions and functions of these proteins can be elucidated genetically by examining the consequences of their malfunction in mutants. This information is important both because it helps elucidate normal function and because it leads to better understanding of the errors that can occur. Errors in chromosome segregation cause a variety of genetic disorders, including Downs Syndrome. The proposed research is designed to investigate the molecular basis of chromosome segregation in yeast. It makes use of mutations in genes that have essential functions during chromosome segregation, including DNA topoisomerase II. It also includes novel method of producing such mutations. This project has four goals: 1) To clarify the role of DNA topoisomerase II in the highly specialized first division of meiosis, using temperature-shift experiments and double-mutant analysis. 2) To investigate the role of topoisomerase II in chromosome structure, by genetically identifying the proteins with which it interacts and analyzing their function. 3) To analyze the molecular function of cdc gene products specifically involved in chromosome segregation, by cloning the genes by complementation, sequencing them, making new mutations by in vitro mutagenesis, and using antibodies to determine the cellular locations of the gene products. 4) To develop a novel method for identifying new mutations affecting gene products that are important for proper chromosome segregation.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM036510-06
Application #
3290610
Study Section
Molecular Biology Study Section (MBY)
Project Start
1986-07-01
Project End
1994-06-30
Budget Start
1991-07-01
Budget End
1992-06-30
Support Year
6
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Harvard University
Department
Type
Schools of Arts and Sciences
DUNS #
071723621
City
Cambridge
State
MA
Country
United States
Zip Code
02138
Adams Martin, A; Dionne, I; Wellinger, R J et al. (2000) The function of DNA polymerase alpha at telomeric G tails is important for telomere homeostasis. Mol Cell Biol 20:786-96
Lavoie, B D; Tuffo, K M; Oh, S et al. (2000) Mitotic chromosome condensation requires Brn1p, the yeast homologue of Barren. Mol Biol Cell 11:1293-304
Merrill, B J; Holm, C (1999) A requirement for recombinational repair in Saccharomyces cerevisiae is caused by DNA replication defects of mec1 mutants. Genetics 153:595-605
Amin, N S; Tuffo, K M; Holm, C (1999) Dominant mutations in three different subunits of replication factor C suppress replication defects in yeast PCNA mutants. Genetics 153:1617-28
Chen, C; Merrill, B J; Lau, P J et al. (1999) Saccharomyces cerevisiae pol30 (proliferating cell nuclear antigen) mutations impair replication fidelity and mismatch repair. Mol Cell Biol 19:7801-15
Merrill, B J; Holm, C (1998) The RAD52 recombinational repair pathway is essential in pol30 (PCNA) mutants that accumulate small single-stranded DNA fragments during DNA synthesis. Genetics 148:611-24
Amin, N S; Holm, C (1996) In vivo analysis reveals that the interdomain region of the yeast proliferating cell nuclear antigen is important for DNA replication and DNA repair. Genetics 144:479-93
Adams, A K; Holm, C (1996) Specific DNA replication mutations affect telomere length in Saccharomyces cerevisiae. Mol Cell Biol 16:4614-20
Johnson, R E; Kovvali, G K; Guzder, S N et al. (1996) Evidence for involvement of yeast proliferating cell nuclear antigen in DNA mismatch repair. J Biol Chem 271:27987-90
McAlear, M A; Tuffo, K M; Holm, C (1996) The large subunit of replication factor C (Rfc1p/Cdc44p) is required for DNA replication and DNA repair in Saccharomyces cerevisiae. Genetics 142:65-78

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