Abstract:
Topologically-associated domains (TADs) are areas of highly associated chromatin that
contribute to the overall 3D structure of chromatin. TADs are demarked by boundaries enriched
with architectural proteins, which insulate TADs, preventing inter-TAD interactions. TADs are
further enriched and insulated by secondary nucleic acid structures known as G-quadruplexes.
The major G-quadruplex helicase is DHX36, which has been shown to impact important cellular
processes such as replication, transcription, translation, and the stress response. However, it is
unknown how the relationship between DHX36 and G-quadruplexes impacts the stability of
TAD boundaries. To better understand this dynamic, we knocked out Dhx36 in mice and
performed high throughput chromosome confirmation (Hi-C) technique. This technique will
allow us to compare TADs in the knockout versus wild-type mice. We expect to find that
knocking out this helicase will improve the stability of G-quadruplexes at TAD boundaries. As a
result, we anticipate a greater number of TADs due to stronger insulation at TAD boundaries. If
our hypothesis is correct, this will suggest DHX36 influences 3D chromatin structure and gene
expression, which will help our understanding in fields such as cancer, aging, and epigenetics.
