Acute BAF perturbation causes immediate changes in chromatin accessibility

Cancer-associated, loss-of-function mutations in genes encoding subunits of the BRG1/BRM-associated factor (BAF) chromatin-remodeling complexes(1-8) often cause drastic chromatin accessibility changes, especially in important regulatory regions(9-19). However, it remains unknown how these changes are established over time (for example, immediate consequences or long-term adaptations), and whether they are causative for intracomplex synthetic lethalities, abro-gating the formation or activity of BAF complexes(9,20-24). In the present study, we use the dTAG system to induce acute degradation of BAF subunits and show that chromatin alterations are established faster than the duration of one cell cycle. Using a pharmacological inhibitor and a chemical degrader of the BAF complex ATPase subunits(25)(,)(26), we show that maintaining genome accessibility requires constant ATP-dependent remodeling. Completely abolishing BAF complex function by acute degradation of a synthetic lethal subunit in a paralog-deficient background results in an almost complete loss of chromatin accessibility at BAF-controlled sites, especially also at superenhancers, providing a mechanism for intracomplex synthetic lethalities.

Automated summary

In this study, the researchers found that chromatin alterations are established faster than the duration of one cell cycle when using the dTAG system to induce acute degradation of BAF subunits. Maintaining genome accessibility was shown to require constant ATP-dependent remodeling, as demonstrated through the use of a pharmacological inhibitor and a chemical degrader of the BAF complex.