Regulation of the 20S proteasome by a novel family of inhibitory proteins

Abstract

The protein degradation machinery plays a critical role in the maintenance of cellular homeostasis, preventing the accumulation of damaged or misfolded proteins and controlling the levels of regulatory proteins. The 20S proteasome degradation machinery is able to cleave any protein with a partially unfolded region, however uncontrolled degradation of the myriad of potential substrates is improbable. Thus, there must exist a regulatory mechanism to control 20S proteasome mediated degradation. Here we have discovered a family of 20S proteasome regulators, named Catalytic Core Regulators (CCRs). They coordinate the function of the 20S proteasome and are involved in the oxidative stress response via Nrf2. The CCRs organize into a feed-forward loop regulatory circuit, with some members stabilizing Nrf2, others being induced by Nrf2, and all of them inhibiting the 20S proteasome. This provides a fine-tuned mechanism to carefully modulate the 20S proteasome, ensuring its proper functioning by controlling the degradative flux.