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Activation of SRK2E/OST1 by ABA & low humidity stress
A, ABA dose response for
SRK2E/OST1 activation
B, ABA-dependent kinase
 activities in the srk2emutant
C, ABA-dependent kinase
activity was not detected in
wild-type leaves
D, ABA-inducible genes were
expressed in wild-type
leaves
E, activation of SRK2E/OST1
by low humidity stress in leaf
tissues
F, kinase activities in the low
 humidity-stressedsrk2e
mutant
G, ABA and OS activated
 SRK2E-GFP inArabidopsis
T87 cells, Cold Stress NOT
Effect of abi and abamutations on the activation of SRK2E/OST1




A, SRK2E-GFP proteins were overexpressed
in abi1–1 andabi2–1                         These results indicate that
                                            two similar PP2C, ABI1 and
B, SRK2E-GFP proteins were overexpressed
in theaba2–1                                ABI2, have distinct roles in
                                            ABA signaling in terms of
C , water loss in abi1–1 and aba2–1mutant   regulation of SRK2E/OST1
seedlings
Structural analysis of the C-terminal region in SnRK2 proteins
A, comparison of the
C-terminal amino acids in
ArabidopsisSnRK2s




B, SRK2D-GFP, SRK2F-GFP,
SRK2G-GFP, and SRK2I-
GFP proteins were over
expressed in T87 cells


C, comparison of the C-
terminal amino acids in
three SnRK2s

Arabidopsis SRK2E/OST1
Fava bean AAPK
RiceSAPK8
The effect of N and C terminus amino acids on
          the activation of SRK2E/OST1
A, schematic representation of the
deletion constructs introduced into
T87 cells

Full-length ,N terminus-deleted, and
two types of C terminus-deleted
SRK2E were designated as2EWT-
GFP ,2EΔN-GFP ,2EΔC1-GFP, and
 2EΔ C2-GFP ,respectively

B, kinase activity of truncated SRK2E/
OST1 in T87 cells

Each construct was overexpressed as
a GFP fusion protein and treated
with ABA )50 M( and sorbitol )0.8M(
for the indicated times, and their cell
 extracts were subjected to
in-gel kinase assay
Functional analysis of truncated SRK2E in the
             complementation of the srk2ephenotype
A ,35S:: 2EWT-GFP srk2eand
35S::2EΔC1-GFP srk2e
seedlings under low humidity
stress
Red triangles indicate wilty
leaves observed in the
35S:: 2EΔ C1-GFP srk2e
plants

B, water loss in each
complementation line

C, effects of ABA on the water
 loss in35S::2EWT-GFP srk2e
 and35S::2EC1-GFP srk2e
plants

D, kinase activity in C terminus-
deleted SRK2E )2EΔC1(
under low humidity stress
Physical interactions between SRK2E/OST1 and ABA
        signaling factors in the yeast two-hybrid assay
A, estimation of partners would
interact with SRK2E/OST1

Interactions between
SRK2E/OST1 and each
signaling factor, including
ABI1, ABI2, AtRac1, and
GPA1, were determined by
growth assay on medium
lacking Leu, Trp, and His in
the presence of 20mM 3-AT

B , effect of the abi1–1mutation
on binding to SRK2E/OST1

Degree of binding to SRK2E/
OST1 was compared
between ABI1 and Abi1–1
by growth assay

 SRK2E/OST1 was used as
     the bait protein
ABI1 physically binds to the C terminus of SRK2E/OST1

A, constructs used for the
identification of the ABI1 binding
domain on SRK2E/OST1

 ,)Full-length )2EWT
 ,)C terminus deleted )(2E-(1–317
 ,)C terminus )(2E-(319 –357
C terminus of SRK2G/OSKL8 )2G-
(311–353(( were used as the prey
proteins

B, identification of the ABI1 binding
domain in SRK2E/OST1

Interactions between ABI1 and each
 construct presented inpanel A
were determined by growth assay
on medium lacking Leu, Trp, and
His in the presence of 20 mM 3-AT
                                        .ABI1 was used as the bait protein
A model to explain SRK2E/OST1 signaling in
                 stomatal closure
When plants sense low humidity stress, the
signal may integrate into two pathways

ABA produced by low humidity may act on
Domain II throughPathway I )(step 3

ABI1 binds to this region and may regulate
SRK2E activity )(step 4

 ABA may also activatePathway II. In this
case, ABI1 and ABI2 may function as negative
regulators )(step 5

On the other hand, the ABA-independent
 pathway specifically acts onDomain I
 throughPathway III )step 7( also regulates
)SRK2E activity )step 8
 )These three pathways converge )steps 5, 9
and result in the complete closure of stomata
Conclusion
  The direct interaction between SRK2E/OST1 and ABI1
through Domain II plays a critical role in the control of
                   stomatal closure

  ABI1 and ABI2 may function as -ve regulators of ABA
                     signaling


 SRK2E without Domain II was activated by low humidity

   Domain II is required for interaction with ABI1 and
                  activation by ABA

Members of SnRK2 family may activate and be activated by
    different downstream and upstream factors

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Functional and physical interaction between srk2 e and abi1

  • 1. Activation of SRK2E/OST1 by ABA & low humidity stress A, ABA dose response for SRK2E/OST1 activation B, ABA-dependent kinase activities in the srk2emutant C, ABA-dependent kinase activity was not detected in wild-type leaves D, ABA-inducible genes were expressed in wild-type leaves E, activation of SRK2E/OST1 by low humidity stress in leaf tissues F, kinase activities in the low humidity-stressedsrk2e mutant G, ABA and OS activated SRK2E-GFP inArabidopsis T87 cells, Cold Stress NOT
  • 2. Effect of abi and abamutations on the activation of SRK2E/OST1 A, SRK2E-GFP proteins were overexpressed in abi1–1 andabi2–1 These results indicate that two similar PP2C, ABI1 and B, SRK2E-GFP proteins were overexpressed in theaba2–1 ABI2, have distinct roles in ABA signaling in terms of C , water loss in abi1–1 and aba2–1mutant regulation of SRK2E/OST1 seedlings
  • 3. Structural analysis of the C-terminal region in SnRK2 proteins A, comparison of the C-terminal amino acids in ArabidopsisSnRK2s B, SRK2D-GFP, SRK2F-GFP, SRK2G-GFP, and SRK2I- GFP proteins were over expressed in T87 cells C, comparison of the C- terminal amino acids in three SnRK2s Arabidopsis SRK2E/OST1 Fava bean AAPK RiceSAPK8
  • 4. The effect of N and C terminus amino acids on the activation of SRK2E/OST1 A, schematic representation of the deletion constructs introduced into T87 cells Full-length ,N terminus-deleted, and two types of C terminus-deleted SRK2E were designated as2EWT- GFP ,2EΔN-GFP ,2EΔC1-GFP, and 2EΔ C2-GFP ,respectively B, kinase activity of truncated SRK2E/ OST1 in T87 cells Each construct was overexpressed as a GFP fusion protein and treated with ABA )50 M( and sorbitol )0.8M( for the indicated times, and their cell extracts were subjected to in-gel kinase assay
  • 5. Functional analysis of truncated SRK2E in the complementation of the srk2ephenotype A ,35S:: 2EWT-GFP srk2eand 35S::2EΔC1-GFP srk2e seedlings under low humidity stress Red triangles indicate wilty leaves observed in the 35S:: 2EΔ C1-GFP srk2e plants B, water loss in each complementation line C, effects of ABA on the water loss in35S::2EWT-GFP srk2e and35S::2EC1-GFP srk2e plants D, kinase activity in C terminus- deleted SRK2E )2EΔC1( under low humidity stress
  • 6. Physical interactions between SRK2E/OST1 and ABA signaling factors in the yeast two-hybrid assay A, estimation of partners would interact with SRK2E/OST1 Interactions between SRK2E/OST1 and each signaling factor, including ABI1, ABI2, AtRac1, and GPA1, were determined by growth assay on medium lacking Leu, Trp, and His in the presence of 20mM 3-AT B , effect of the abi1–1mutation on binding to SRK2E/OST1 Degree of binding to SRK2E/ OST1 was compared between ABI1 and Abi1–1 by growth assay SRK2E/OST1 was used as the bait protein
  • 7. ABI1 physically binds to the C terminus of SRK2E/OST1 A, constructs used for the identification of the ABI1 binding domain on SRK2E/OST1 ,)Full-length )2EWT ,)C terminus deleted )(2E-(1–317 ,)C terminus )(2E-(319 –357 C terminus of SRK2G/OSKL8 )2G- (311–353(( were used as the prey proteins B, identification of the ABI1 binding domain in SRK2E/OST1 Interactions between ABI1 and each construct presented inpanel A were determined by growth assay on medium lacking Leu, Trp, and His in the presence of 20 mM 3-AT .ABI1 was used as the bait protein
  • 8. A model to explain SRK2E/OST1 signaling in stomatal closure When plants sense low humidity stress, the signal may integrate into two pathways ABA produced by low humidity may act on Domain II throughPathway I )(step 3 ABI1 binds to this region and may regulate SRK2E activity )(step 4 ABA may also activatePathway II. In this case, ABI1 and ABI2 may function as negative regulators )(step 5 On the other hand, the ABA-independent pathway specifically acts onDomain I throughPathway III )step 7( also regulates )SRK2E activity )step 8 )These three pathways converge )steps 5, 9 and result in the complete closure of stomata
  • 9. Conclusion The direct interaction between SRK2E/OST1 and ABI1 through Domain II plays a critical role in the control of stomatal closure ABI1 and ABI2 may function as -ve regulators of ABA signaling SRK2E without Domain II was activated by low humidity Domain II is required for interaction with ABI1 and activation by ABA Members of SnRK2 family may activate and be activated by different downstream and upstream factors