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Photosynthetic-product-dependent Activation of Plasma Membrane H + -ATPase and Nitrate Uptake in Arabidopsis Leaves
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Abstract
Plasma membrane (PM) H
+
-ATPase is a pivotal enzyme for plant growth and development that acts as a primary transporter and is activated by phosphorylation of the penultimate residue, threonine, at the C-terminus. Photosynthetically active radiation activates PM H
+
-ATPase via phosphorylation in mesophyll cells of
Arabidopsis thaliana
, and phosphorylation of PM H
+
-ATPase depends on photosynthesis and photosynthesis-related sugar supplementation, such as sucrose, fructose and glucose. However, the molecular mechanism and the physiological role of photosynthesis-dependent PM H
+
-ATPase activation are still unknown. Analysis using sugar analogues, such as palatinose, turanose, and 2-deoxy glucose, revealed that sucrose metabolites and products of glycolysis such as pyruvate induce phosphorylation of PM H
+
-ATPase. Transcriptome analysis showed that novel isoform of the
Small Auxin Up RNA
genes,
SAUR30
, is upregulated in a light- and sucrose-dependent manner. Time course analyzes of sucrose supplementation showed that phosphorylation level of PM H
+
-ATPase increased within 10 min, but expression level of
SAUR30
increased later than 10 min. The results suggest two temporal regulations may participate in the regulation of PM H
+
-ATPase. Interestingly, a
15
NO
3
-
uptake assay in leaves showed that light increases
15
NO
3
-
uptake, and that increment of
15
NO
3
-
uptake depends on PM H
+
-ATPase activity. The results opened the possibility of physiological role of photosynthesis-dependent PM H
+
-ATPase activation in the uptake of NO
3
-
. We speculate that PM H
+
-ATPase may connect photosynthesis and nitrogen metabolism in leaves.
Title: Photosynthetic-product-dependent Activation of Plasma Membrane H
+
-ATPase and Nitrate Uptake in Arabidopsis Leaves
Description:
Abstract
Plasma membrane (PM) H
+
-ATPase is a pivotal enzyme for plant growth and development that acts as a primary transporter and is activated by phosphorylation of the penultimate residue, threonine, at the C-terminus.
Photosynthetically active radiation activates PM H
+
-ATPase via phosphorylation in mesophyll cells of
Arabidopsis thaliana
, and phosphorylation of PM H
+
-ATPase depends on photosynthesis and photosynthesis-related sugar supplementation, such as sucrose, fructose and glucose.
However, the molecular mechanism and the physiological role of photosynthesis-dependent PM H
+
-ATPase activation are still unknown.
Analysis using sugar analogues, such as palatinose, turanose, and 2-deoxy glucose, revealed that sucrose metabolites and products of glycolysis such as pyruvate induce phosphorylation of PM H
+
-ATPase.
Transcriptome analysis showed that novel isoform of the
Small Auxin Up RNA
genes,
SAUR30
, is upregulated in a light- and sucrose-dependent manner.
Time course analyzes of sucrose supplementation showed that phosphorylation level of PM H
+
-ATPase increased within 10 min, but expression level of
SAUR30
increased later than 10 min.
The results suggest two temporal regulations may participate in the regulation of PM H
+
-ATPase.
Interestingly, a
15
NO
3
-
uptake assay in leaves showed that light increases
15
NO
3
-
uptake, and that increment of
15
NO
3
-
uptake depends on PM H
+
-ATPase activity.
The results opened the possibility of physiological role of photosynthesis-dependent PM H
+
-ATPase activation in the uptake of NO
3
-
.
We speculate that PM H
+
-ATPase may connect photosynthesis and nitrogen metabolism in leaves.
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