description): The objective of this proposal is to understand the molecular mechanisms involved in methylation dependent transcriptional repression. In vertebrates, methylated DNA is generally ordered into transcriptionally inactive repressive chromatin structures. Methylation patterns change during the course of early development. However, alterations in normal methylation status may have disastrous consequences. Xenopus laevis is the ideal organism for studying events and components involved in methylation-dependent silencing. It provides a wealth of endogenous proteins for biochemical approaches as well as an established development from embryo to adult. My long term goal is to establish myself as an independent researcher. I would like my lab to focus on studying the roles of chromatin and methylation in gene regulation through development.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Career Transition Award (K22)
Project #
1K22HD001338-01
Application #
6024669
Study Section
Special Emphasis Panel (ZHD1-MCHG-B (PJ))
Program Officer
Moody, Sally Ann
Project Start
2002-08-21
Project End
2004-07-31
Budget Start
2002-08-21
Budget End
2003-07-31
Support Year
1
Fiscal Year
2002
Total Cost
$134,520
Indirect Cost
Name
University of Illinois Urbana-Champaign
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
041544081
City
Champaign
State
IL
Country
United States
Zip Code
61820
LONG, Steven W; Ooi, Jenny Y Y; Yau, Peter M et al. (2011) A brain-derived MeCP2 complex supports a role for MeCP2 in RNA processing. Biosci Rep 31:333-43
Long, Steven W; Ooi, Jenny Y Y; Yau, Peter M et al. (2011) A brain-derived MeCP2 complex supports a role for MeCP2 in RNA processing. Biosci Rep 31:333-43