TY - JOUR
T1 - Visualizing Ca2+ signatures in plants
AU - Monshausen, Gabriele B.
N1 - Funding Information:
This work was supported by National Science Foundation grant MCB-1121994 .
PY - 2012/12
Y1 - 2012/12
N2 - Ca2+ is a key player in an astonishing variety of plant signal transduction pathways where transient, spiking or oscillatory changes in cytosolic Ca2+ levels help to couple environmental or developmental cues to appropriate cellular responses. Understanding whether and how much Ca2+ signaling contributes to defining stimulus-response specificity has long been a challenge, but recent work has provided strong evidence that specific information can indeed be encoded in the spatiotemporal characteristics of Ca2+ signals. Identification of the Ca2+ binding proteins that transduce Ca2+ signals by regulating downstream effector proteins has revealed a complex network of Ca2+ sensor families, of which some members show distinct patterns of expression and subcellular localization. By utilizing genetically encoded fluorescent Ca2+ probes to monitor Ca2+ changes at high spatiotemporal resolution, it is now possible to explore whether such spatial heterogeneities in Ca2+ sensor distribution are coordinated with subcellular microdomains of Ca2+ signaling. Such visualization of Ca2+ signaling will also help to address which cellular compartments and transporters contribute to mobilizing and sequestering Ca2+ and thus define stimulus-specific Ca2+ signatures.
AB - Ca2+ is a key player in an astonishing variety of plant signal transduction pathways where transient, spiking or oscillatory changes in cytosolic Ca2+ levels help to couple environmental or developmental cues to appropriate cellular responses. Understanding whether and how much Ca2+ signaling contributes to defining stimulus-response specificity has long been a challenge, but recent work has provided strong evidence that specific information can indeed be encoded in the spatiotemporal characteristics of Ca2+ signals. Identification of the Ca2+ binding proteins that transduce Ca2+ signals by regulating downstream effector proteins has revealed a complex network of Ca2+ sensor families, of which some members show distinct patterns of expression and subcellular localization. By utilizing genetically encoded fluorescent Ca2+ probes to monitor Ca2+ changes at high spatiotemporal resolution, it is now possible to explore whether such spatial heterogeneities in Ca2+ sensor distribution are coordinated with subcellular microdomains of Ca2+ signaling. Such visualization of Ca2+ signaling will also help to address which cellular compartments and transporters contribute to mobilizing and sequestering Ca2+ and thus define stimulus-specific Ca2+ signatures.
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U2 - 10.1016/j.pbi.2012.09.014
DO - 10.1016/j.pbi.2012.09.014
M3 - Review article
C2 - 23044039
AN - SCOPUS:84870517345
SN - 1369-5266
VL - 15
SP - 677
EP - 682
JO - Current Opinion in Plant Biology
JF - Current Opinion in Plant Biology
IS - 6
ER -