Discovery and heterologous reconstitution of a plant noncanonical quasi-circadian gene regulatory network
Summary
Circadian rhythms are mainly generated by a gene regulatory network (GRN) constituted by transcription factors (TFs). Comparisons between plant and mammalian circadian clock GRNs suggest conservation of the network architecture rather than its components. Therefore, a rhythm-generating capacity is not restricted to canonical circadian clock GRNs. Here, we showed that although the circadian clock GRN was arrhythmic, circadian rhythms were maintained in refrigerated postharvest strawberries.
Content
# Discovery and heterologous reconstitution of a plant noncanonical quasi-circadian gene regulatory network
*Published: 2026 May 12*
Circadian rhythms are mainly generated by a gene regulatory network (GRN)
constituted by transcription factors (TFs). Comparisons between plant and
mammalian circadian clock GRNs suggest conservation of the network architecture
rather than its components. Therefore, a rhythm-generating capacity is not
restricted to canonical circadian clock GRNs. Here, we showed that although the
circadian clock GRN was arrhythmic, circadian rhythms were maintained in
refrigerated postharvest strawberries. Through systematic dual-luciferase assays
and network analysis, we discovered a noncanonical GRN pillared by five
uncharacterized TFs. We developed a heterologous reconstitution system and
demonstrated the rhythm-generating ability of this GRN. Subsequent systematic
evolution of ligands by exponential enrichment followed by high-throughput
sequencing (SELEX-seq), electrophoretic mobility shift assay (EMSA), and DNA
affinity purification (DAP)-qPCR analyses suggested that this GRN was
responsible for the circadian rhythms of downstream genes. Fruit-specific
perturbation of this GRN led to enhanced susceptibility to Botrytis cinerea.
Collectively, our study identified a noncanonical quasi-circadian GRN, realized
the heterologous reconstitution of eukaryotic circadian GRNs, and demonstrated
its function in immune regulation.
DOI: 10.1016/j.cell.2026.04.033