Many genetic disorders, including cancer, can result from the translocation of genes to novel chromatin environments that influence the fidelity of their expression. Position effect variegation (PEV) is a well documented and described phenomenon that results from the repression of genes that have been inserted within or juxtaposed near heterochromatin, following a chromosomal translocation or inversion. The research proposed here should elucidate a more clear understanding of the protein machinery involved in the formation of gene repressive heterochromatin, their influence on PEV and the manner in which individual protein constituents interact with one another within heterochromatin. Furthermore, I will test the possibility that gene repressive heterochromatin can be established selectively in the genome, providing the skeletal framework for gene therapy in patients suffering from genetic disorders where the expression of a mutated or translocated gene is detrimental.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32GM019849-02
Application #
6150777
Study Section
Biological Sciences 2 (BIOL)
Program Officer
Wolfe, Paul B
Project Start
1999-02-01
Project End
Budget Start
2000-02-01
Budget End
2001-01-31
Support Year
2
Fiscal Year
2000
Total Cost
$37,516
Indirect Cost
Name
Fred Hutchinson Cancer Research Center
Department
Type
DUNS #
075524595
City
Seattle
State
WA
Country
United States
Zip Code
98109
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Smothers, J F; Henikoff, S (2000) The HP1 chromo shadow domain binds a consensus peptide pentamer. Curr Biol 10:27-30