Cells 2012, 1(4), 738-753; doi:10.3390/cells1040738
Review

Intricately Regulated: A Cellular Toolbox for Fine-Tuning XBP1 Expression and Activity

Department of Microbiology and Immunology, College of Medicine, University of South Alabama, Mobile, AL 36688, USA
* Author to whom correspondence should be addressed.
Received: 10 August 2012; Accepted: 25 September 2012 / Published: 15 October 2012
(This article belongs to the Special Issue Cellular Stress Response)
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Abstract: Stress in the endoplasmic reticulum (ER) triggers the unfolded protein response (UPR), a signaling mechanism that allows cellular adaptation to ER stress by engaging pro-adaptive transcription factors and alleviating protein folding demand. One such transcription factor, X-box binding protein (XBP1), originates from the inositol-requiring transmembrane kinase/endoribonuclease 1 (IRE1) UPR stress sensor. XBP1 up-regulates a pool of genes involved in ER protein translocation, protein folding, vesicular trafficking and ER- associated protein degradation. Recent data suggest that the regulation of XBP1 expression and transcriptional activity may be a tissue- and stress-dependent phenomenon. Moreover, the intricacies involved in “fine-tuning” XBP1 activity in various settings are now coming to light. Here, we provide an overview of recent developments in understanding the regulatory mechanisms underlying XBP1 expression and activity and discuss the significance of these new insights.
Keywords: endoplasmic reticulum; endoplasmic reticulum stress; unfolded protein response; XBP1

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MDPI and ACS Style

Byrd, A.E.; Brewer, J.W. Intricately Regulated: A Cellular Toolbox for Fine-Tuning XBP1 Expression and Activity. Cells 2012, 1, 738-753.

AMA Style

Byrd AE, Brewer JW. Intricately Regulated: A Cellular Toolbox for Fine-Tuning XBP1 Expression and Activity. Cells. 2012; 1(4):738-753.

Chicago/Turabian Style

Byrd, Andrew E.; Brewer, Joseph W. 2012. "Intricately Regulated: A Cellular Toolbox for Fine-Tuning XBP1 Expression and Activity." Cells 1, no. 4: 738-753.

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