| Abstrakt: |
SUMMARY: Precise regulation of flowering time is critical for cereal crops to synchronize reproductive development with optimum environmental conditions, thereby maximizing grain yield. The plant‐specific gene GIGANTEA (GI) plays an important role in the control of flowering time, with additional functions on the circadian clock and plant stress responses. In this study, we show that GI loss‐of‐function mutants in a photoperiod‐sensitive tetraploid wheat background exhibit significant delays in heading time under both long‐day (LD) and short‐day photoperiods, with stronger effects under LD. However, this interaction between GI and photoperiod is no longer observed in isogenic lines carrying either a photoperiod‐insensitive allele in the PHOTOPERIOD1 (PPD1) gene or a loss‐of‐function allele in EARLY FLOWERING 3 (ELF3), a known repressor of PPD1. These results suggest that the normal circadian regulation of PPD1 is required for the differential effect of GI on heading time in different photoperiods. Using crosses between mutant or transgenic plants of GI and those of critical genes in the flowering regulation pathway, we show that GI accelerates wheat heading time by promoting FLOWERING LOCUS T1 (FT1) expression via interactions with ELF3, VERNALIZATION 2 (VRN2), CONSTANS (CO), and the age‐dependent microRNA172‐APETALA2 (AP2) pathway, at both transcriptional and protein levels. Our study reveals conserved GI mechanisms between wheat and Arabidopsis but also identifies specific interactions of GI with the distinctive photoperiod and vernalization pathways of the temperate grasses. These results provide valuable knowledge for modulating wheat heading time and engineering new varieties better adapted to a changing environment. Significance Statement: The role of GIGANTEA (GI) in the Arabidopsis photoperiodic pathway is well characterized, but its role in the divergent photoperiodic pathway of the temperate grasses remains unknown. We demonstrate that, in wheat, GI promotes heading time through multiple interconnected pathways, including grass‐specific interactions with the vernalization gene VRN2 and with PPD1, the key gene in wheat photoperiod pathway, as well as complex interactions with ELF3, CO, and the miR172‐AP2 pathway that are conserved with Arabidopsis. [ABSTRACT FROM AUTHOR] |
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