The long-term objective of this work is to understand how a eukaryotic chromosome replicates. To this end, a replication map of chromosome III of the yeast, Saccharomyces cerevisiae, has been prepared. This map includes the positions of ARS elements, detected by their ability to promote the autonomous replication of plasmids, the positions of DNA replication origins, detected by 2D gel analysis of replication intermediates, and the positions of DNA replication termination. This proposal addresses three major issues concerning the replication and maintenance of chromosome III. First, both genetic and molecular approaches will be used to study the mechanism(s) by which a derivative of this chromosome lacking active chromosomal replicators. Second, the mechanism(s) by which chromosomal replicator activity is influenced by chromosomal context will be studied by examining the temporal pattern of replication of the chromosome and by using several genetic and molecular approaches designed to map the determinants of replicator activity. Finally, the structure of several chromosome III replicators will be further defined using both genetic and biochemical approaches. The binding sites for the replicator initiator protein, ORC, will be identified, and novel proteins that bind to replicators will be sought with a genetic screen. Replication timing determinants in ARS301 will be identified, and the role of ARS304 in the function of the recombination enhancer that activates HML as a donor of information in mating type switching will be analyzed. These studies will provide new insights into a fundamental cellular process, chromosome replication. Knowledge gained from the genetically tractable yeast system is applicable to larger eukaryotes, and guides the approaches to these experimentally difficult systems. The proposed studies are also likely to lead to a further understanding of chromosome rearrangements and the reactivation of DNA replication that are characteristics of malignant cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM035679-17
Application #
6385598
Study Section
Special Emphasis Panel (ZRG1-BM-2 (01))
Program Officer
Wolfe, Paul B
Project Start
1985-04-01
Project End
2003-07-31
Budget Start
2001-08-01
Budget End
2002-07-31
Support Year
17
Fiscal Year
2001
Total Cost
$585,864
Indirect Cost
Name
University of Medicine & Dentistry of NJ
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
605799469
City
Newark
State
NJ
Country
United States
Zip Code
07107
Irene, Carmela; Theis, James F; Gresham, David et al. (2016) Hst3p, a histone deacetylase, promotes maintenance of Saccharomyces cerevisiae chromosome III lacking efficient replication origins. Mol Genet Genomics 291:271-83
Theis, James F; Irene, Carmela; Dershowitz, Ann et al. (2010) The DNA damage response pathway contributes to the stability of chromosome III derivatives lacking efficient replicators. PLoS Genet 6:e1001227
Chang, Fujung; Theis, James F; Miller, Jeremy et al. (2008) Analysis of chromosome III replicators reveals an unusual structure for the ARS318 silencer origin and a conserved WTW sequence within the origin recognition complex binding site. Mol Cell Biol 28:5071-81
Caldwell, Julie M; Chen, Yinhuai; Schollaert, Kaila L et al. (2008) Orchestration of the S-phase and DNA damage checkpoint pathways by replication forks from early origins. J Cell Biol 180:1073-86
Theis, James F; Dershowitz, Ann; Irene, Carmela et al. (2007) Identification of mutations that decrease the stability of a fragment of Saccharomyces cerevisiae chromosome III lacking efficient replicators. Genetics 177:1445-58
Dershowitz, Ann; Snyder, Marylynn; Sbia, Mohammed et al. (2007) Linear derivatives of Saccharomyces cerevisiae chromosome III can be maintained in the absence of autonomously replicating sequence elements. Mol Cell Biol 27:4652-63
Newlon, Carol S; Theis, James F (2002) DNA replication joins the revolution: whole-genome views of DNA replication in budding yeast. Bioessays 24:300-4
Fabiani, L; Irene, C; Aragona, M et al. (2001) A DNA replication origin and a replication fork barrier used in vivo in the circular plasmid pKD1. Mol Genet Genomics 266:326-35
Poloumienko, A; Dershowitz, A; De, J et al. (2001) Completion of replication map of Saccharomyces cerevisiae chromosome III. Mol Biol Cell 12:3317-27
Malkova, A; Signon, L; Schaefer, C B et al. (2001) RAD51-independent break-induced replication to repair a broken chromosome depends on a distant enhancer site. Genes Dev 15:1055-60

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