Proapoptotic BAX and BAK modulate the unfolded protein response by a direct interaction with IRE1α

Claudio Hetz, Paula Bernasconi, Jill Fisher, Ann Hwee Lee, Michael C. Bassik, Bruno Antonsson, Gabriel S. Brandt, Neal N. Iwakoshi, Anna Schrinzel, Laurie H. Glimcher, Stanley J. Korsmeyer

Research output: Contribution to journalArticlepeer-review

573 Scopus citations

Abstract

Accumulation of misfolded protein in the endoplasmic reticulum (ER) triggers an adaptive stress response-termed the unfolded protein response (UPR)-mediated by the ER transmembrane protein kinase and endoribonuclease inositol-requiring enzyme-1α (IRE1α). We investigated UPR signaling events in mice in the absence of the proapoptotic BCL-2 family members BAX and BAK [double knockout (DKO)]. DKO mice responded abnormally to tunicamycin-induced ER stress in the liver, with extensive tissue damage and decreased expression of the IRE1 substrate X-box-binding protein 1 and its target genes. ER-stressed DKO cells showed deficient IRE1α signaling. BAX and BAK formed a protein complex with the cytosolic domain of IRE1α that was essential for IRE1α activation. Thus, BAX and BAK function at the ER membrane to activate IRE1α signaling and to provide a physical link between members of the core apoptotic pathway and the UPR.

Original languageEnglish (US)
Pages (from-to)572-576
Number of pages5
JournalScience
Volume312
Issue number5773
DOIs
StatePublished - Apr 28 2006
Externally publishedYes

Fingerprint

Dive into the research topics of 'Proapoptotic BAX and BAK modulate the unfolded protein response by a direct interaction with IRE1α'. Together they form a unique fingerprint.

Cite this