The Role of Water Channel Proteins in Facilitating Recovery of Leaf Hydraulic Conductance from Water Stress in <i>Populus trichocarpa</i>

<div><p>Gas exchange is constrained by the whole-plant hydraulic conductance (<i>K</i>_plant). Leaves account for an important fraction of <i>K</i>_plant and may therefore represent a major determinant of plant productivity. Leaf hydraulic conductance (<i>K</i>_leaf) decreases with increasing water stress, which is due to xylem embolism in leaf veins and/or the properties of the extra-xylary pathway. Water flow through living tissues is facilitated and regulated by water channel proteins called aquaporins (AQPs). Here we assessed changes in the hydraulic conductance of <i>Populus trichocarpa</i> leaves during a dehydration-rewatering episode. While leaves were highly sensitive to drought, <i>K</i>_leaf recovered only 2 hours after plants were rewatered. Recovery of <i>K</i>_leaf was absent when excised leaves were bench-dried and subsequently xylem-perfused with a solution containing AQP inhibitors. We examined the expression patterns of 12 highly expressed AQP genes during a dehydration-rehydration episode to identify isoforms that may be involved in leaf hydraulic adjustments. Among the AQPs tested, several genes encoding tonoplast intrinsic proteins (TIPs) showed large increases in expression in rehydrated leaves, suggesting that TIPs contribute to reversing drought-induced reductions in <i>K</i>_leaf. TIPs were localized in xylem parenchyma, consistent with a role in facilitating water exchange between xylem vessels and adjacent living cells. Dye uptake experiments suggested that reversible embolism formation in minor leaf veins contributed to the observed changes in <i>K</i>_leaf.</p>