We identified a novel protein, designated Thap11 (Thanatos-associated protein 11) in hES cells. Thap11 isan inhibitor of differentiation in ES cells. In contrast to most other factors, Thap11 seems to be directlyinvolved with both, transcriptional control and epigenetic modification. Thapl 1 has a putative DMA-bindingdomain that shows significant similarity to the DMA-binding domain of the Drosophila P element (a DMAtransposon). This suggested that, like the P element, Thapl 1 might act as a site-specific transcriptionalmodulator, a possibility we subsequently confirmed. Interestingly, one of the genes most strikinglyupregulated by Thapl 1 in ES cells is Suz12 (Suppressor of Zeste 12, epigenetic modifier that suppressesdifferentiation in hES cells). In addition Thapl 1 interacts with DMA methyltransferase like protein 3(DnmtSL), and has its own NAD+-dependent histone deacetylase (HDAC) activity, making it a novel HDACin its own right.Our overall hypothesis is that Thapl 1 plays a critical role in controlling self-renewal of hES cells byblocking differentiation. To test this hypothesis will (a) analyze how Thapl 1 controls the expression ofSuz12 and identify additional target genes of Thapl 1; knowledge of these genes (including Suz12) iscritical since they are part of the transcriptional network that controls the undifferentiated state(pluripotency) of hES cells; (b) dissect the relationship between Thapl 1 and DnmtSL; we will study howThapl 1 interacts with DnmtSL and if this modulates site-specific DMA methylation of genes (Suz12 andothers); (c) analyze the NAD+-dependent HDAC activity of Thapl 1. This information will allow us tomodulate Thapl 1's HDAC activity, an effect that in turn should help control differentiation of hES cells if ourprimary Hypothesis is correct.Since Thapl 1 acts as a transcriptional factor and is also involved in at least two epigenetic mechanisms,DNA methylation and histone deacetylation, it may represent an important link between transcriptionalcontrol and epigenetics in hES cells. Specific genetic and pharmacologic interventions targeting Thapl1function may allow control of self-renewal and differentiation of hES cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Program Projects (P01)
Project #
1P01GM081627-01
Application #
7356524
Study Section
Special Emphasis Panel (ZGM1-GDB-8 (SC))
Project Start
Project End
Budget Start
2007-09-01
Budget End
2008-08-31
Support Year
1
Fiscal Year
2007
Total Cost
$227,521
Indirect Cost
Name
Baylor College of Medicine
Department
Type
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
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