SAUR65 is part of the SAUR gene family, which comprises growth regulators critical for differential organ development in response to light and auxin. In Arabidopsis, SAUR65 belongs to Class 3 of the lirSAURs (light-induced in cotyledons and/or repressed in hypocotyls SAURs), a subgroup whose expression correlates with organ-specific growth patterns during dark-to-light transitions .
SAUR65 overexpression (e.g., 35S:SAUR65-GFP lines) significantly enhances cell expansion:
| Parameter | Wild Type (WT) | SAUR65 Overexpression |
|---|---|---|
| Hypocotyl length | 10.2 mm | 14.8 mm (+45%) |
| Cotyledon area | 3.2 mm² | 4.7 mm² (+47%) |
| Epidermal cell size | 120 µm² | 180 µm² (+50%) |
These phenotypes arise from SAUR65’s role in promoting cell wall acidification via H+-ATPase activation, which drives osmotic water uptake and cell expansion .
SAUR65 interacts with D-clade type 2C protein phosphatases (PP2C.Ds), inhibiting their activity to derepress plasma membrane H+-ATPases . Key mechanistic insights include:
| Interaction Partner | Effect | Functional Outcome |
|---|---|---|
| PP2C-D1 | Inhibition of phosphatase activity | Increased H+-ATPase activity |
| PP2C-D2 | No direct inhibition | Context-dependent regulation |
SAUR65 competes with inhibitory SAURs (e.g., SAUR50) for PP2C-D binding, modulating growth asymmetry in apical hooks and cotyledons during photomorphogenesis .
SAUR65 expression is tightly controlled by light and auxin:
Light regulation: Repressed in hypocotyls but induced in cotyledons during dark-to-light transitions .
Auxin sensitivity: Part of a broader SAUR network integrating hormonal and environmental signals .
While no commercial SAUR65 antibody is explicitly described in the literature, studies utilize transgenic approaches (e.g., GFP fusions) to track SAUR65 localization and function . Key findings include:
Antagonistic interactions with other SAURs (e.g., SAUR17) to balance growth suppression and activation .