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Salinity-Induced Palmella Formation Mechanism in Halotolerant Algae Dunaliella salina Revealed by Quantitative Proteomics and Phosphoproteomics

Overview of attention for article published in Frontiers in Plant Science, May 2017
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Title
Salinity-Induced Palmella Formation Mechanism in Halotolerant Algae Dunaliella salina Revealed by Quantitative Proteomics and Phosphoproteomics
Published in
Frontiers in Plant Science, May 2017
DOI 10.3389/fpls.2017.00810
Pubmed ID
Authors

Sijia Wei, Yangyang Bian, Qi Zhao, Sixue Chen, Jiawei Mao, Chunxia Song, Kai Cheng, Zhen Xiao, Chuanfang Zhang, Weimin Ma, Hanfa Zou, Mingliang Ye, Shaojun Dai

Abstract

Palmella stage is critical for some unicellular algae to survive in extreme environments. The halotolerant algae Dunaliella salina is a good single-cell model for studying plant adaptation to high salinity. To investigate the molecular adaptation mechanism in salinity shock-induced palmella formation, we performed a comprehensive physiological, proteomics and phosphoproteomics study upon palmella formation of D. salina using dimethyl labeling and Ti(4+)-immobilized metal ion affinity chromatography (IMAC) proteomic approaches. We found that 151 salinity-responsive proteins and 35 salinity-responsive phosphoproteins were involved in multiple signaling and metabolic pathways upon palmella formation. Taken together with photosynthetic parameters and enzyme activity analyses, the patterns of protein accumulation and phosphorylation level exhibited the mechanisms upon palmella formation, including dynamics of cytoskeleton and cell membrane curvature, accumulation and transport of exopolysaccharides, photosynthesis and energy supplying (i.e., photosystem II stability and activity, cyclic electron transport, and C4 pathway), nuclear/chloroplastic gene expression regulation and protein processing, reactive oxygen species homeostasis, and salt signaling transduction. The salinity-responsive protein-protein interaction (PPI) networks implied that signaling and protein synthesis and fate are crucial for modulation of these processes. Importantly, the 3D structure of phosphoprotein clearly indicated that the phosphorylation sites of eight proteins were localized in the region of function domain.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 65 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 65 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 9 14%
Student > Bachelor 8 12%
Researcher 7 11%
Professor > Associate Professor 7 11%
Student > Master 7 11%
Other 17 26%
Unknown 10 15%
Readers by discipline Count As %
Agricultural and Biological Sciences 18 28%
Biochemistry, Genetics and Molecular Biology 17 26%
Engineering 3 5%
Environmental Science 2 3%
Chemistry 2 3%
Other 6 9%
Unknown 17 26%
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 08 June 2017.
All research outputs
#18,554,389
of 22,979,862 outputs
Outputs from Frontiers in Plant Science
#13,915
of 20,425 outputs
Outputs of similar age
#238,988
of 313,707 outputs
Outputs of similar age from Frontiers in Plant Science
#465
of 593 outputs
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So far Altmetric has tracked 20,425 research outputs from this source. They receive a mean Attention Score of 4.0. This one is in the 20th percentile – i.e., 20% of its peers scored the same or lower than it.
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We're also able to compare this research output to 593 others from the same source and published within six weeks on either side of this one. This one is in the 13th percentile – i.e., 13% of its contemporaries scored the same or lower than it.