Hi my name is Carly Hom and I am an undergraduate student researcher at
Arizona State University working with Dr. Karmella Haynes. In my current
lab I am using Synthetic Biology and Bioinformatics to investigate reliable
and predictable reactivation of dormant genes that can help treat cancer
and enable tissue re-growth. By determining which silenced genes will
switch to an active state in osteosarcoma cells, with the presence of the
synthetic transcription factor PC-TF, my work will establish a
comprehensive method for predicting the effect of rationally designed
protein-based drugs. Pc-TF, a synthetic transcription factor developed by
Dr. Haynes, regulates cell states by binding the repressive
trimethyl-histone H3 lysine 27 signal (H3K27me3) and switching silenced
genes to an active state in osteosarcoma cells. Since a comprehensive ChIP
map is not available for osteosarcoma, I will be identifying genes
associated with H3K27me3 in liver (HepG2) and fibroblast (BJ) cell lines.
Overall, I will need to collect about 1000 genes from the ENCODE database
that show a significant enough H3K27me3 signal at the promoter of the gene.
I have already figured out how to project only information from the HepG2
and BJ cell lines in relation to H3K27me3, but by just clicking to move
through the cell line to find genes will take entirely too long and can
cause me to miss important genes. At the request of Dr. Haynes I am asking
if ENCODE has some sort of filter program that will provide a list of genes
where the promoter site shows a high level of the H3K27me3 histone
methylation. I will need it to be able to find the beginning of the gene's
promoter on the UCSC Genome Browser and then show about 500bps to the left
and 500bps to the right of the promoter . Ultimately, I want to be able to
navigate through the genes in this cell line that show a significant enough
H3K27me3 signal at the promoter (everything else with a low H3K27me3 signal
I do not care about). If you could get back to me on whether this is even
possible to do within the Genome Browser, and if yes, how I would be able
to do this that would be great. Thank you!

- Carly Hom

-- 
Caroline Hom
Tempe, AZ
Ph: 602-315-5728
Arizona State University
Ira A. Fulton Schools of Engineering
Biomedical Engineering
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