A Tandem Amino Acid Residue Motif in Guard Cell SLAC1 Anion Channel of Grasses Allows for the Control of Stomatal Aperture by Nitrate

A Tandem Amino Acid Residue Motif in Guard Cell SLAC1 Anion Channel of Grasses Allows for the Control of Stomatal Aperture by Nitrate
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DOI:
10.1016/j.cub.2018.03.027
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发表时间:
2018-05
期刊:
影响因子:
9.2
通讯作者:
Nadine Schäfer;T. Maierhofer;Johannes Herrmann;M. E. Jørgensen;Christof Lind;K. Meyer;S. Lautner
Nadine Schäfer;T. Maierhofer;Johannes Herrmann;M. E. Jørgensen;Christof Lind;K. Meyer;S. Lautner
中科院分区:
生物学1区
文献类型:
--
作者:
Nadine Schäfer;T. Maierhofer;Johannes Herrmann;M. E. Jørgensen;Christof Lind;K. Meyer;S. Lautner

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The latest major group of plants to evolve were the grasses. These became important in the mid-Paleogene about 40 million years ago. During evolution, leaf CO2uptake and transpirational water loss were optimized by the acquisition of grass-specific stomatal complexes. In contrast to the kidney-shaped guard cells (GCs) typical of the dicots such asArabidopsis, in the grasses and agronomically important cereals, the GCs are dumbbell shaped and are associated with morphologically distinct subsidiary cells (SCs). We studied the molecular basis of GC action in the major cereal crop barley. Upon feeding ABA to xylem sap of an intact barley leaf, stomata closed in a nitrate-dependent manner. This process was initiated by activation of GC SLAC-type anion channel currents. HvSLAC1 expressed inXenopusoocytes gave rise to S-type anion currents that increased several-fold upon stimulation with >3 mM nitrate. We identified a tandem amino acid residue motif that within the SLAC1 channels differs fundamentally between monocots and dicots. When the motif of nitrate-insensitive dicotArabidopsisSLAC1 was replaced by the monocot signature, AtSLAC1 converted into a grass-type like nitrate-sensitive channel. Our work reveals a fundamental difference between monocot and dicot GCs and prompts questions into the selective pressures during evolution that resulted in fundamental changes in the regulation of SLAC1 function.