Abscisic acid dynamics in roots detected with genetically encoded FRET sensors

被引:187
作者
Jones, Alexander M. [1 ]
Danielson, Jonas A. H. [1 ]
ManojKumar, Shruti N. [1 ]
Lanquar, Viviane [1 ]
Grossmann, Guido [1 ,2 ]
Frommer, Wolf B. [1 ]
机构
[1] Carnegie Inst Sci, Dept Plant Biol, Stanford, CA 94305 USA
[2] Heidelberg Univ, Cluster Excellence CellNetworks, Ctr Organismal Studies, Heidelberg, Germany
来源
ELIFE | 2014年 / 3卷
基金
瑞典研究理事会; 美国国家科学基金会;
关键词
ACTIVATED PROTEIN-KINASES; OSMOTIC-STRESS RESPONSES; IN-VIVO; SELECTIVE ACTIVATION; ARABIDOPSIS MUTANTS; ABA BIOSYNTHESIS; SEED DORMANCY; SNRK2; KINASES; WATER-STRESS; SALT STRESS;
D O I
10.7554/eLife.01741
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cytosolic hormone levels must be tightly controlled at the level of influx, efflux, synthesis, degradation and compartmentation. To determine ABA dynamics at the single cell level, FRET sensors (ABACUS) covering a range similar to 0.2-800 mu M were engineered using structure-guided design and a high-throughput screening platform. When expressed in yeast, ABACUS1 detected concentrative ABA uptake mediated by the AIT1/NRT1.2 transporter. Arabidopsis roots expressing ABACUS1-2 mu (K-d similar to 2 mu M) and ABACUS1-80 mu (K-d similar to 80 mu M) respond to perfusion with ABA in a concentration-dependent manner. The properties of the observed ABA accumulation in roots appear incompatible with the activity of known ABA transporters (AIT1, ABCG40). ABACUS reveals effects of external ABA on homeostasis, that is, ABA-triggered induction of ABA degradation, modification, or compartmentation. ABACUS can be used to study ABA responses in mutants and quantitatively monitor ABA translocation and regulation, and identify missing components. The sensor screening platform promises to enable rapid fine-tuning of the ABA sensors and engineering of plant and animal hormone sensors to advance our understanding of hormone signaling.
引用
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页数:30
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