PROJECT SUMMARY
The evolutionarily conserved SWI/SNF chromatin remodeler, exists as distinct polymorphic complexes,
BAF, PBAF and ncBAF, each with differing subunit composition. Though these complexes share a
common biological function of altering chromatin architecture, it is the unique subunits within each form
of SWI/SNF that help define their genomic roles. With the identification of SWI/SNF as a tumor
suppressor, a lot of attention has been focused on how loss of subunits leverage the remaining
complexes for transcriptional output. However, focusing attention on a normal cell that needs to
constantly adjust transcriptional output to respond to a variety of external stimuli, an interesting question
remains: How do cells dynamically alter the usage of the various SWI/SNF complexes for gene
expression and do they achieve this dynamic usage by changing the amounts of each form of the
complex within cells. We have leveraged hypoxia as an environmental stimulus to address this very
question. Our preliminary studies show that hypoxic cells retain BAF and ncBAF proteins at levels similar
to those in normoxic cells, but decrease levels of PBAF members, while displaying a dependence on
BAF for expression of hypoxic genes. The overall goal of this proposal is to gain mechanistic
understanding of the dynamic regulation and usage of various forms of SWI/SNF as a response to
environmental cues, specifically hypoxic exposure. In AIM 1, we will define the composition of the various
forms of SWI/SNF, during hypoxic response, with emphasis on how varying levels of oxygen
concentration affects SWI/SNF complex levels, using both 2D and 3D cell culture models. In AIM 2, we
ask how cells use the altered stoichiometry of SWI/SNF forms for regulation of hypoxic gene expression.
In AIM 3, we seek to define the molecular mechanisms of downregulation of PBAF during hypoxia. Our
studies, will cumulatively provide a mechanistic understanding of how cells dynamically utilize the various
forms of SWI/SNF to respond to changing environmental signals. Given that many chromatin modifiers
exist in a plurality of forms, our studies will help identify mechanisms that may commonly be in play to
regulate functions and usage of these important enzyme complexes.