Deletions and sequence mutations of genes are the mechanisms typically considered when evaluating the etiology and progression of neoplasia. This topic has been extensively examined over the past several decades. Likewise, genetic instability as manifested by development of numerical and structural alterations of chromosomes is also a typical feature of cancer development that has been the subject of intense study. More recently it has been recognized that many cancers manifest alterations in gene expression that are not coincident with gene mutations. These changes are thought to be associated with alterations of DNA methylation in the promoter of these genes and by histone modifications at the sites of these promoters. There have been far fewer efforts to identify the mechanisms that can explain these latter types of cancer-related changes. In this project we seek to understand mechanisms that can explain the transition of alleles of non-imprinted genes from synchronous to non-synchronous replication timing in carcinogenesis. While it is known that such shifts in replication timing can lead to the alterations in gene expression seen in many types of cancers, the exact mechanisms responsible for the conservation of replication timing are not known. Others and we found that both DNA replication and transcription are often initiated in or near the gene promoter and associated CpG island. In this project we seek to better define the essential genomic elements required for the function of DNA replication origins found at transcriptional promoters. We also pose the following questions: Do differences in origin firing times correspond to differences in the binding time of specific factors necessary for origin activation? Are there sites in normal human cells that slow or pause the progression of DNA replication forks? Are such sites involved in the regulation of the order of activation time of adjacent origins of DNA replication? To gain insights into these mechanisms and answer these questions we propose the following Specific Aims.
Specific Aim 1 : Characterize genetic elements necessary for activity of the HPRT origin of replication.
Specific Aim 2 : Analyze binding of the pre-replication complex at the HPRT and G6PD origins of replication on the active and the inactive X chromosome in female human cells.
Specific Aim 3 : Analyze the architecture of replication and potential fork progression barriers in an early replicated region of the human genome.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
2R01CA084493-05A1
Application #
6920930
Study Section
Cancer Genetics Study Section (CG)
Program Officer
Pelroy, Richard
Project Start
1999-12-01
Project End
2010-03-31
Budget Start
2005-04-08
Budget End
2006-03-31
Support Year
5
Fiscal Year
2005
Total Cost
$282,405
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Pathology
Type
Schools of Medicine
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Kaufman, David G; Cohen, Stephanie M; Chastain, Paul D (2011) Temporal and functional analysis of DNA replicated in early S phase. Adv Enzyme Regul 51:257-71
Luke, April M; Chastain, Paul D; Pachkowski, Brian F et al. (2010) Accumulation of true single strand breaks and AP sites in base excision repair deficient cells. Mutat Res 694:65-71
Asagoshi, Kenjiro; Tano, Keizo; Chastain 2nd, Paul D et al. (2010) FEN1 functions in long patch base excision repair under conditions of oxidative stress in vertebrate cells. Mol Cancer Res 8:204-15
Chastain 2nd, Paul D; Nakamura, Jun; Rao, Shangbang et al. (2010) Abasic sites preferentially form at regions undergoing DNA replication. FASEB J 24:3674-80
Cohen, Stephanie M; Chastain 2nd, Paul D; Rosson, Gary B et al. (2010) BRG1 co-localizes with DNA replication factors and is required for efficient replication fork progression. Nucleic Acids Res 38:6906-19
Frum, Rebecca A; Khondker, Zakaria S; Kaufman, David G (2009) Temporal differences in DNA replication during the S phase using single fiber analysis of normal human fibroblasts and glioblastoma T98G cells. Cell Cycle 8:3133-48
Frum, Rebecca A; Chastain 2nd, Paul D; Qu, Pingping et al. (2008) DNA replication in early S phase pauses near newly activated origins. Cell Cycle 7:1440-8
Kaufman, David G; Cordeiro-Stone, Marila; Brylawski, Bruna P et al. (2007) Early S phase DNA replication: a search for targets of carcinogenesis. Adv Enzyme Regul 47:127-38
Cohen, Stephanie M; Cordeiro-Stone, Marila; Kaufman, David G (2007) Early replication and the apoptotic pathway. J Cell Physiol 213:434-9
Brylawski, Bruna P; Chastain 2nd, Paul D; Cohen, Stephanie M et al. (2007) Mapping of an origin of DNA replication in the promoter of fragile X gene FMR1. Exp Mol Pathol 82:190-6

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