BBX proteins promote HY5-mediated UVR8 signaling in Arabidopsis

Plants undergo photomorphogenic development in the presence of light. Photomorphogenesis is repressed by the E3 ubiquitin ligase CONSTITUTIVELY PHOTOMORPHOGENIC1 (COP1), which binds substrates through their valine-proline (VP) motifs. The UV RESISTANCE LOCUS8 (UVR8) photoreceptor senses UV-B and inhibits COP1 through cooperative binding of its own VP motif mimicry and its photosensing core to COP1, thereby preventing COP1 binding to substrates, including the bZIP transcriptional regulator ELONGATED HYPOCOTYL5 (HY5). As a key promoter of visible light and UV-B photomorphogenesis, HY5 functions together with the B-box family transcription factors BBX20-22 that were recently described as HY5 rate-limiting coactivators under red light. Here we describe a hypermorphic bbx21-3D mutant with enhanced photomorphogenesis, which carries a proline-314 to leucine mutation in the VP motif that impairs interaction with and regulation through COP1. We show that BBX21 and BBX22 are UVR8-dependently stabilized after UV-B exposure, which is counteracted by a repressor induced by HY5/BBX activity. bbx20 bbx21 bbx22 mutants under UV-B are impaired in hypocotyl growth inhibition, photoprotective pigment accumulation, and expression of several HY5-dependent genes. We conclude that BBX20-22 importantly contribute to HY5 activity in a subset of UV-B responses, but that additional, presently unknown coactivators for HY5 are functional in early UVR8 signaling.