We conducted a comprehensive analysis of transcription of two candidate histone methyltransferases in human and mouse tissues, revealing tissue-specific expression of alternatively spliced and read-through transcripts. A major fraction of read-through transcripts may add an encoded protein domain modifying specificity of one the candidates. A manuscript is in preparation on this work. We conducted several yeast two-hybrid screens to identify protein-binding partners for the putative histone methyltransferases. These screens yielded several intriguing candidates that are being characterized further by biochemical and genetic methods in mammalian cells and in vitro. We have generated a conditional knockout mouse model lacking one of the putative histone methyltransferases located on a frequently deleted chromosomal region. The knockout mice could comprise a new model for chronic lymphocytic leukemia, for asthma, and/or for other cancers or human diseases.

Agency
National Institute of Health (NIH)
Institute
Division of Basic Sciences - NCI (NCI)
Type
Intramural Research (Z01)
Project #
1Z01BC010631-02
Application #
7292925
Study Section
(MCGP)
Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
2005
Total Cost
Indirect Cost
Name
Basic Sciences
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Van Duyne, Rachel; Easley, Rebecca; Wu, Weilin et al. (2008) Lysine methylation of HIV-1 Tat regulates transcriptional activity of the viral LTR. Retrovirology 5:40