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Updated: Jan 3, 2026

A High Resolution Method to Monitor Phosphorylation-dependent Activation of IRF3
Published on: January 24, 2016
IRF4 Activity Is Required in Established Plasma Cells to Regulate Gene Transcription and Mitochondrial Homeostasis
Michael Sze Yuan Low1, Erica J Brodie2, Pasquale L Fedele3
1Walter and Eliza Hall Institute of Medical Research, 1G Royal Parade, Parkville 3052, VIC, Australia; Monash Haematology, Monash Health, 246 Clayton Road, Clayton 3168, VIC, Australia; Department of Immunology and Pathology, Monash University, 89 Commercial Road, Melbourne 3004, VIC, Australia; School of Clinical Sciences at Monash Health, Centre for Cancer Research, Hudson Institute of Medical Research, Monash University, Clayton 3168, VIC, Australia; Department of Medical Biology, University of Melbourne, Melbourne 3010, VIC, Australia.
Abstract:
The transcription factor interferon regulatory factor 4 (IRF4) is critical for the development, maintenance, and function of plasma cells. The mechanism by which IRF4 exerts its action in mature plasma cells has been elusive due to the death of all such cells upon IRF4 loss. While we identify apoptosis as a critical pathway for the death of plasma cells caused by IRF4 loss, we also determine that IRF4 did not regulate the intrinsic apoptotic pathway directly. By using an inducible IRF4 deletion system in the presence of the overexpression of anti-apoptotic BCL2, we identify genes whose expression is coordinated by IRF4 and that in turn specify plasma cell identity and mitochondrial homeostasis.
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