期刊
TRENDS IN BIOCHEMICAL SCIENCES
卷 39, 期 5, 页码 245-254出版社
ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.tibs.2014.02.008
关键词
endoplasmic reticulum stress; unfolded protein response; RNase; IRE1; RIDD
资金
- INSERM
- INCa
- CRLCC Eugene Marquis
- FWO
lnositol-requiring enzyme 1 (IRE1) is the most conserved transducer of the unfolded protein response (UPR), a homeostatic response that preserves proteostasis. Intriguingly, via its endoribonuclease activity, IRE1 produces either adaptive or death signals. This occurs through both unconventional splicing of XBP1 mRNA and regulated IRE1-dependent decay of mRNA (RIDD). Whereas XBP1 mRNA splicing is cytoprotective in response to endoplasmic reticulum (ER) stress, RIDD has revealed many unexpected features. For instance, RIDD cleaves RNA at an XBP1-like consensus site but with an activity divergent from XBP1 mRNA splicing and can either preserve ER homeostasis or induce cell death. Here we review recent findings on RIDD and propose a model of how IRE1 RNase activity might control cell fate decisions.
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