• What is the problem/issue being addressed?
Plants lack a nervous system and central decision-making organ, but can nevertheless sense and respond to environmental cues, including seasonal cues that play crucial roles in regulating their growth and development, through poorly understood mechanisms. By exploring the interplay between gene expression, hormonal regulation, and cell-cell communication, we elucidated the mechanisms underlying the temperature-mediated control of bud dormancy. In this project we have provided an important insight into the molecular regulation of dormancy and the mechanism underlying seasonally aligned growth in trees by temperature.
• Why is it important for society?
In this project we have identified the role of AGL8-GA module in mediating PD opening and provided an important insight into the molecular regulation of dormancy and the mechanism underlying seasonally aligned growth in trees by temperature. This research project revealed the mysteries behind bud dormancy in trees by investigating the interactions between genes, hormones, and cell-cell communication. These findings will advance our understanding of how plants adapt to seasonal changes and contribute to the competitiveness of European research, particularly in the field of developmental adaptation to seasonal variations.
• What are the overall objectives?
This project aims to elucidate the molecular mechanisms underlying the temperature-mediated control of bud dormancy in the experimental model tree hybrid aspen. In this project we functionally characterized an unknown MADS-box transcription factor AGL8, which was previously identified in the host lab. In this project we focused on (1) If FT1 is a direct downstream target of AGL8 and AGL8-mediated FT1 activation is required for low temperature (LT) induced dormancy release, (2) If AGL8 is a LT-responsive transcriptional regulator of GA biosynthesis in buds, and if AGL8-mediated LT-induced GA biosynthesis is essential for LT-induced dormancy release, and (3) Whether AGL8 promotes dormancy release by transcriptionally activating the expression of GH17 endoglucanases which are believed to catalyse callose breakdown and a subsequent PD opening.