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Calcium Efflux Systems in Stress Signaling and Adaptation in Plants

Overview of attention for article published in Frontiers in Plant Science, January 2011
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Title
Calcium Efflux Systems in Stress Signaling and Adaptation in Plants
Published in
Frontiers in Plant Science, January 2011
DOI 10.3389/fpls.2011.00085
Pubmed ID
Authors

Jayakumar Bose, Igor I. Pottosin, Stanislav S. Shabala, Michael G. Palmgren, Sergey Shabala

Abstract

Transient cytosolic calcium ([Ca(2+)](cyt)) elevation is an ubiquitous denominator of the signaling network when plants are exposed to literally every known abiotic and biotic stress. These stress-induced [Ca(2+)](cyt) elevations vary in magnitude, frequency, and shape, depending on the severity of the stress as well the type of stress experienced. This creates a unique stress-specific calcium "signature" that is then decoded by signal transduction networks. While most published papers have been focused predominantly on the role of Ca(2+) influx mechanisms to shaping [Ca(2+)](cyt) signatures, restoration of the basal [Ca(2+)](cyt) levels is impossible without both cytosolic Ca(2+) buffering and efficient Ca(2+) efflux mechanisms removing excess Ca(2+) from cytosol, to reload Ca(2+) stores and to terminate Ca(2+) signaling. This is the topic of the current review. The molecular identity of two major types of Ca(2+) efflux systems, Ca(2+)-ATPase pumps and Ca(2+)/H(+) exchangers, is described, and their regulatory modes are analyzed in detail. The spatial and temporal organization of calcium signaling networks is described, and the importance of existence of intracellular calcium microdomains is discussed. Experimental evidence for the role of Ca(2+) efflux systems in plant responses to a range of abiotic and biotic factors is summarized. Contribution of Ca(2+)-ATPase pumps and Ca(2+)/H(+) exchangers in shaping [Ca(2+)](cyt) signatures is then modeled by using a four-component model (plasma- and endo-membrane-based Ca(2+)-permeable channels and efflux systems) taking into account the cytosolic Ca(2+) buffering. It is concluded that physiologically relevant variations in the activity of Ca(2+)-ATPase pumps and Ca(2+)/H(+) exchangers are sufficient to fully describe all the reported experimental evidence and determine the shape of [Ca(2+)](cyt) signatures in response to environmental stimuli, emphasizing the crucial role these active efflux systems play in plant adaptive responses to environment.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 226 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Portugal 2 <1%
United States 1 <1%
Italy 1 <1%
Norway 1 <1%
Unknown 221 98%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 48 21%
Student > Master 36 16%
Researcher 32 14%
Student > Bachelor 16 7%
Student > Doctoral Student 15 7%
Other 39 17%
Unknown 40 18%
Readers by discipline Count As %
Agricultural and Biological Sciences 115 51%
Biochemistry, Genetics and Molecular Biology 41 18%
Environmental Science 5 2%
Computer Science 4 2%
Engineering 3 1%
Other 14 6%
Unknown 44 19%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 02 December 2011.
All research outputs
#20,165,369
of 22,675,759 outputs
Outputs from Frontiers in Plant Science
#15,745
of 19,843 outputs
Outputs of similar age
#169,848
of 180,328 outputs
Outputs of similar age from Frontiers in Plant Science
#39
of 50 outputs
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So far Altmetric has tracked 19,843 research outputs from this source. They receive a mean Attention Score of 4.0. This one is in the 1st percentile – i.e., 1% of its peers scored the same or lower than it.
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