
Dimerization of IRE1α is not sufficient for its phosphorylation and activation. Higher-order oligomerization is necessary to trigger cross-phosphorylation and unleash the full endonuclease activity of IRE1α.


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The unfolded protein response can switch from a pro-survival to a maladaptive, pro-apoptotic mode. During endoplasmic reticulum (ER) stress, IRE1α sensors dimerize, are phosphorylated and activate XBP1 splicing, increasing folding capacity in the ER protein factory. The steps that turn the IRE1α endonuclease activity against endogenous mRNAs during maladaptive ER stress are still unknown. Here we show that although necessary, IRE1α dimerization is not sufficient to trigger phosphorylation. Random and/or guided collisions amongst IRE1α dimers are needed to elicit cross-phosphorylation and endonuclease activities. Thus, reaching a critical concentration of IRE1α dimers in the ER membrane is a key event. Formation of stable IRE1α clusters is not necessary for RNase activity. However, clustering could modulate the potency of the response promoting interactions between dimers and decreasing the accessibility of phosphorylated IRE1α to phosphatases. The stepwise activation of IRE1α molecules and their low concentration at steady state prevent excessive responses, unleashing full-blown IRE1 activity only upon intense stress conditions.

*   UPR
    :   unfolded protein response
    ER
    :   endoplasmic reticulum
    ERAD
    :   ER-associated degradation
    IRE1
    :   Inositol-requiring enzyme type 1

Congress of multiple dimers is needed for cross-phosphorylation of IRE1α and its RNase activity

phosphorylation-and-oligomerization-are-key-steps-in-the-activation-of-the-endoplasmic-reticulum-stress-sensor-ire1α


Phosphorylation and Oligomerization are Key Steps in the Activation of the Endoplasmic Reticulum Stress Sensor IRE1α
