Abstract

Thellungiella halophila, a close relative of Arabidopsis, is a model halophyte used to study plant salt tolerance. The proteomic/physiological/transcriptomic analyses of Thellungiella plant leaves subjected to different salinity levels, reported herein, indicate an extraordinary ability of Thellungiella to adapt to large concentrations of exogenous saline by compartmentalizing Na(+) into cell vacuoles and accumulating proline and soluble sugars as organic osmolytes. Salinity stress stimulated the accumulation of starch in chloroplasts, which resulted in a greatly increased content of starch and total sugars in leaves. Comparative proteomics of Thellungiella leaves identified 209 salt-responsive proteins. Among these, the sequences of 108 proteins were strongly homologous to Arabidopsis protein sequences, and 30 had previously been identified as Thellungiella proteins. Functional classification of these proteins into 16 categories indicated that the majority are involved in carbohydrate metabolism, followed by those involved in energy production and conversion, and then those involved in the transport of inorganic ions. Pathway analysis revealed that most of the proteins are involved in starch and sucrose metabolism, carbon fixation, photosynthesis, and glycolysis. Of these processes, the most affected were starch and sucrose metabolism, which might be pivotal for salt tolerance. The gene expression patterns of the 209 salt-responsive proteins revealed through hierarchical clustering of microarray data and the expression patterns of 29 Thellungiella genes evaluated via quantitative RT-PCR were similar to those deduced via proteomic analysis, which underscored the possibility that starch and sucrose metabolism might play pivotal roles in determining the salt tolerance ability of Thellungiella. Our observations enabled us to propose a schematic representation of the systematic salt-tolerance phenotype in Thellungiella and suggested that the increased accumulation of starch, soluble sugars, and proline, as well as subcellular compartmentalization of sodium, might collectively denote important mechanisms for halophyte salt tolerance.

Highlights

  • From the ‡Key Laboratory of Biology and Genetic Resources for Tropical Crops, Institute of Tropical Biosciences and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, Hainan 571101, China; §Hainan University, Haikou, Hainan 570228, China; ʈKey Laboratory of Photobiology, Institute of Botany, Chinese Academy of Sciences, Beijing 100093, China

  • Our results demonstrate that salt treatment greatly reduced its growth, the plant was able to survive at 600 mM NaCl (Fig. 1A)

  • Many plants use changes in ion homeostasis, osmotic adjustment, injury avoidance, and growth adjustment to cope with salinity stress (2, 6)

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Summary

The abbreviations used are

2-DE, two-dimensional electrophoresis; COG, cluster of orthologous groups; CPS, counts per second; DW, dry weight; FW, fresh weight; GO, gene ontology; Mr, molecular weight; MS, mass spectrometry; P5CD, 1-pyrroline-5-carboxylate dehydrogenase; pI, isoelectric point; qRT-PCR, quantitative real-time transcription polymerase chain reaction; ROS, reactive oxygen species; S.D., standard deviation; SEM, scanning electron microscopy; SOS, salt overly sensitive; TCA, tricarboxylic acid; TEM, transmission electron microscopy; TWC, total water content. By removing interfering compounds and salt ions (19), the BPP method enabled a comparative proteomic analysis of S. europaea grown under different levels of salinity (20). We further compared the technical details in Coomassie Brilliant Blue staining and developed the more sensitive protocol GAP, which uses Coomassie Brilliant Blue G-250, ammonium sulfate, and phosphoric acid (21). These technical improvements allowed us to integrate comparative proteomic, transcriptomic, and physiological analyses for Thellungiella rosette leaves exposed to different saline levels. Leaf proteins were extracted using the BPP protocol (19) and separated by means of 2-DE, with the gels stained by GAP (21). We can propose a schematic of the mechanistic basis of salt tolerance in Thellungiella and suggest that the accumulation of large amounts of cellular starch and soluble sugars might be the key mechanism that confers salt tolerance on halophytes

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