Gene silencing events associated with promoter region methylation are common in malignant cells. An unresolved issue for these silencing events is whether promoter region methylation represents the beginning or end of the process. The major goal of this application is to use mouse Aprt to demonstrate that promoter region methylation is the endpoint of a multistep silencing process. Specifically, methyl binding proteins (MBPs), which are known to bind to methylated regions within the genome and to attract repressive complexes, will be used to trigger silencing at a distance from the promoter. Additional experiments will demonstrate that the promoter has a significant, yet imperfect, mechanism to block MBP-induced silencing and that selective processes are sufficient to maintain silencing. Finally, it will be shown that promoter region methylation is the inevitable endpoint of the silencing process, and that this late event serves to stabilize chromatin changes that accompany MBP-mediated silencing at distance. The demonstration of each step of a multistep silencing pathway, which is currently undefined, will provide novel insight into this aberrant process in malignant cells.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA092114-02
Application #
6515172
Study Section
Pathology B Study Section (PTHB)
Program Officer
Okano, Paul
Project Start
2001-07-01
Project End
2004-06-30
Budget Start
2002-07-01
Budget End
2003-06-30
Support Year
2
Fiscal Year
2002
Total Cost
$237,825
Indirect Cost
Name
Oregon Health and Science University
Department
Neurosciences
Type
Schools of Medicine
DUNS #
009584210
City
Portland
State
OR
Country
United States
Zip Code
97239
Oyer, Jon A; Yates, Phillip A; Godsey, Sarah et al. (2011) Aberrantly silenced promoters retain a persistent memory of the silenced state after long-term reactivation. Mutat Res 706:21-7
Yates, Phillip A; Burman, Robert; Simpson, James et al. (2003) Silencing of mouse Aprt is a gradual process in differentiated cells. Mol Cell Biol 23:4461-70
Turker, Mitchell S (2002) Gene silencing in mammalian cells and the spread of DNA methylation. Oncogene 21:5388-93