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examination of stomatal opening of
35S::LLA23
leaves showed that
approximately 86% (78/91) of
35S::LLA23E
stomata remained open under
drought stresses for 12 days, a percentage close to 96% (74/77) of the wild-
type stomata without stress (Fig.
2
.
3
F). The unexpected observation of sto-
matal opening was further checked by measuring the levels of ABA of both
plant types. Correlated with the opening of
35S::LLA23
stomata, the trans-
genic plants did not appreciably increase their ABA levels upon drought
stresses for 12 d, similar to that of the wild-type plants at normal growth
conditions (
Yang et al., 2005
). It clearly indicated that due to the pres-
ence of LLA23 proteins, the response to ABA was delayed in the transgenic
plants upon water deficit. The LLA23 protein functions as a water-retaining
molecule that confers drought resistance on
35S::LLA23
plants based on
the drought test of transgenic lines, in which leaves of these plants overex-
pressing LLA23 protein had lower rates of water loss than wild-type plants
(Fig.
2
.
3
E), while
35S::LLA23
stomata remained open upon drought
stresses for 12 days. Nevertheless, if these plants were continued to withhold
water for additional 4 days, most
35S::LLA23
stomata (87%) became closed
(Fig.
2
.
3
F); transgenic plants began to wilt and their ABA levels in leaves
markedly increased.
The transpiration rate of transgenic plants was also examined. As
shown in Fig.
2
.
4
A,
35S::LLA23
leaves showed pattern of transpiration
rate similar to the wild-type leaves upon drought stress despite that 91%
(91/100) of
35S::LLA23E
stomata remained open, which is opposite to
83% (88/106) of the closed stomata observed in the wild-type leaves (Fig.
2
.
4
B). It is rational that ABA in the wild-type leaves was apparently pro-
duced and let most stomata (88/106) become closed upon drought stress
while under the same drought condition, ABA in the transgenic plants did
not change, similar to the unstressed wild-type plants and thus most sto-
mata (91/100) remained disclosed. The fact that LLA23-overexpressing
plants kept approximately the same transpiration rate as the wild-type plants
while their stomata mostly remained open strongly suggests the function
of LLA23 as a water-retaining molecule in the
35S::LLA23
leaves. It cor-
relates with the results obtained when the rate of water loss from detached
leaves of wild-type and LLA23-overexpressing plants was compared (Fig.
2
.
3
E). The
gin1-3
mutant, however, displayed a much more pronounced
transpiration rate because the mutant was unable to produce ABA to which
stomata respond and thus, 96% (78/82) of
gin1-3
stomata remained open
(Fig.
2
.
4
B). In addition to acting as a water-retaining molecule, the LLA23
protein may protect other macromolecules from losing their biological
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