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A Bioluminescent Reporter System for Real-Time Monitoring of the Unfolded Protein Response in Plants.

Liu Y, Niu Y, Zhao Y, Zhang W, Lv Y, Liu M, Zhang Q, Wang J, Zhang X, Li Y, Zhang H, Zhang Y, Bao Y.

Plant biotechnology journal · 24 Mar 2026 · 10.1111/pbi.70631

Abstract

The unfolded protein response (UPR) is a critical mechanism for maintaining endoplasmic reticulum (ER) homeostasis under stress. Here, we developed a bioluminescent reporter system, AtbZIP60-LUC, in Arabidopsis to dynamically monitor ER stress by coupling IRE1-mediated splicing of bZIP60 mRNA to firefly luciferase (LUC) expression. Under ER stress, IRE1 removes a 23-bp sequence from bZIP60u, producing a spliced bZIP60s transcript in-frame with LUC, enabling luciferin-dependent luminescence. Transgenic AtbZIP60-LUC lines exhibited specificity for canonical ER stressors (heat, DTT, tunicamycin) but not osmotic stressors (NaCl, mannitol), confirmed by bioluminescence, qPCR, and immunoblotting. Time-course assays revealed rapid LUC induction by DTT (peak at 1 h) and delayed activation by tunicamycin (peak at 1-2 h), followed by signal decline, reflecting adaptive UPR dynamics. Heat stress optimization identified 38°C as optimal, inducing robust LUC expression after 2-3 h without compromising viability, while 42°C caused irreversible damage. Genetic validation in ire1a ire1b mutants abolished LUC induction, confirming IRE1 dependency, whereas constitutive UPR activation via maize 16-kDa γ-zein (16γz) overexpression triggered LUC expression without stress. Extending this system to tobacco and tomato, we engineered NbbZIP60-LUC and SlbZIP60-LUC, which similarly responded to heat (38°C), DTT, tunicamycin, and ER-localized protein aggregation (16γz, zeolin) in transient and stable assays. This work establishes bZIP60-LUC as versatile, non-invasive tools for real-time UPR monitoring in plants, offering insights into ER stress dynamics and enabling cross-species studies of stress adaptation mechanisms.

Code and data availability

The article describes a bZIP60-LUC bioluminescent reporter study with bioluminescence imaging, qPCR, and immunoblotting data. No public phenotype dataset, image/sensor inputs, author analysis code, or trained model is deposited; the Data Availability Statement only points to the main text and Supporting Information (a

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