IRE1α controls cyclin A1 expression and promotes cell proliferation through XBP-1

Jeffery A. Thorpe, Steven R. Schwarze

Research output: Contribution to journalArticlepeer-review

63 Scopus citations


IRE1 is a conserved dual endoribonuclease/protein kinase that is indispensable for directing the endoplasmic reticulum (ER) stress response in yeast, flies, and worms. In mammalian systems, however, the precise biological activities carried out by IRE1α are unclear. Here, molecular and chemical genetic approaches were used to control IRE1 activity in a number of prostate cancer cell lines and the resulting impact on gene transcription, cell survival, and proliferation was examined. Modulating IRE1α activity had no transcriptional effect on the induction of genes classically associated with the ER stress response (Grp78 and CHOP) or cell survival when confronted with ER stress agents. Rather, IRE1α activity was positively correlated to proliferation. Since Xbp-1 mRNA is the sole known substrate for IRE1 endoribonuclease activity, the role of this transcription factor in mediating proliferation was examined. Repressing total Xbp-1 levels by siRNA techniques effectively slowed proliferation. In an effort to identify IRE1/XBP-1 targets responsible for the cell cycle response, genome-wide differential mRNA expression analysis was performed. Consistent with its ability to sense ER stress, IRE1α induction led to an enrichment of ER-Golgi, plasma membrane, and secretory gene products. An increase in cyclin A1 expression was the only differentially expressed cell cycle regulatory gene found. Greater cyclin A protein levels were consistently observed in cells with active IRE1α and were dependent on XBP-1. We conclude that IRE1α activity controls a subset of the ER stress response and mediates proliferation through tight control of Xbp-1 splicing.

Original languageEnglish
Pages (from-to)497-508
Number of pages12
JournalCell Stress and Chaperones
Issue number5
StatePublished - Sep 2010

Bibliographical note

Funding Information:
Acknowledgements This work was supported by the New York Academy of Medicine (SRS).


  • Cyclin A
  • ER stress
  • IRE1
  • Proliferation
  • XBP-1

ASJC Scopus subject areas

  • Biochemistry
  • Cell Biology


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