Mitogen-activated protein kinase action in plant response to high-temperature stress: a mini review.

In recent years, extreme weather events such as high temperature (HT) are becoming more frequent. HT has become one of the main environmental factors affecting crop growth and development. In nature, plant cells initiate corresponding tolerant mechanisms by sensing and transducing HT signals. The mitogen-activated protein kinase (MAPK) cascade is widely involved in the signal transduction of plants to various environmental stresses. MAPK-mediated HT responses have attracted more and more attention. We herein focus on the current state of knowledge of MAPK in the plant under HT stress and summarize the mechanisms of MAPK in HT response from Ca2+ signal, reactive oxygen species (ROS) signal, heat shock transcription factor and heat shock protein, antioxidant system, and the direct downstream targets of MAPK. This review encapsulates the known plant MAPK cascade and provides prospects for ongoing research on HT response.

In-depth proteome analysis reveals multiple pathways involved in tomato SlMPK1-mediated high-temperature responses.

High temperature (HT) is one of the major environmental factors which limits plant growth and yield. The mitogen-activated protein kinase (MAPK) plays vital roles in environmental stress responses. However, the mechanisms triggered by MAPKs in plants in response to HT are still extremely limited. In this study, the proteomic data of differences between SlMPK1 RNA-interference mutant (SlMPK1i) and wild type and of tomato (Solanum lycopersicum) plants under HT stress using isobaric tags for relative and absolute quantitation (iTRAQ) was re-analyzed in depth. In total, 168 differently expressed proteins (DEPs) were identified in response to HT stress, including 38 DEPs only found in wild type, and 84 DEPs specifically observed in SlMPK1i after HT treatment. The majority of higher expression of 84 DEPs were annotated into photosynthesis, oxidation-reduction process, protein folding, translation, proteolysis, stress response, and amino acid biosynthetic process. More importantly, SlMPK1-mediated photosynthesis was confirmed by the physiological characterization of SlMPK1i with a higher level of photosynthetic capacity under HT stress. Overall, the results reveal a set of potential candidate proteins helping to further understand the intricate regulatory network regulated by SlMPK1 in response to HT.

Transcriptome -wide modulation combined with morpho-physiological analyses of Typha orientalis roots in response to lead challenge.

Lead (Pb) is a common pollutant in many environments, including in the soil, water, and/or air. Typha orientalis Presl, a large emergent aquatic plant, has been reported to function as a Pb-tolerant and Pb-accumulating plant; however, very little molecular information regarding the tolerance of T. orientalis towards Pb is known. In this study, Pb accumulation and key factors involved in the Pb stress response at different Pb concentrations were investigated. Pb was primarily accumulated in the roots and was mainly located in the cell wall and membrane systems. Differentially expressed genes (DEGs) were identified in T. orientalis roots after Pb exposure via RNA-seq analyses. In the 0.10 mM and 0.25 mM Pb2+-treated groups, a total of 3275 DEGs were detected relative to the control. Many of these genes were associated with oxidation-reduction processes, metal transport, protein kinase/phosphorylation, and DNA binding transcription factors, which were shown to be Pb-responsive DEGs. Mapping Kyoto Encyclopedia of Genes and Genomes (KEGG) database, "phenylpropanoid biosynthesis" was analyzed as the major pathway of the important modules of overlapping DEGs of 0.10 mM and 0.25 mM Pb2+ treatments. Furthermore, a lead response gene named ToLR1 with unknown function was of particular interest. The full-length of ToLR1 sequence was cloned using rapid amplification of cDNA ends (RACE) and overexpressed in Arabidopsis thaliana, which resulted in enhanced resistance to Pb stress. This is the first report providing genomic information detailing Pb responsive genes in T. orientalis. Moreover, this study provides novel insights into the molecular mechanisms underlying the response of T. orientalis and other accumulators towards Pb stress. The key genes identified in this study may serve as potential targets for genetic engineering targeting phytoremediation.

Genome-wide analysis of the plant-specific VQ motif-containing proteins in tomato (Solanum lycopersicum) and characterization of SlVQ6 in thermotolerance.

The VQ motif-containing (VQ) proteins are plant-specific proteins with a conserved "FxxhVQxhTG" amino acid sequence, which regulate plant growth and development. Little is known, however, about the function of VQ proteins in tomato (Solanum lycopersicum). Here, a total of 26 SlVQ proteins were confirmed and characterized using a comprehensive genome-wide analysis. The SlVQ proteins all contain the conserved motif with seven variations, which are classified into eight groups (I, II, IV-VI, VIII-X). Most of them were predicted to be localized in the nucleus. Besides, a network including SlVQ proteins interaction with WRKY transcription factors (SlWRKYs) and mitogen-activated protein kinases (SlMPKs) is proposed. In addition, among the SlVQ genes, SlVQ6 was expressed in the range of organs and tissues with the highest levels and could response to different stresses. Ectopically overexpression of SlVQ6 in Arabidopsis plants decreased high temperature tolerance. RNA sequencing analysis revealed that several stress-related genes, such as HSP70-4, RD20, GolS1 and AT4g36010 were down-regulated in SlVQ6 overexpressing plants compared to these in wild-type under normal growth conditions. This study provides critical information about SlVQ genes and their encoded proteins, as well as further research on SlVQ functions in tomato growth and development.

Proteomic analysis by iTRAQ-PRM provides integrated insight into mechanisms of resistance in pepper to Bemisia tabaci (Gennadius).

BACKGROUND: The Bemisia tabaci is a major leaf feeding insect pest to pepper (Capsicum annuum), causing serious damage to pepper growth and yield. It is particularly important to study the mechanism of pepper resistance to B. tabaci, and to breed and promote the varieties of pepper resistant to B. tabaci. However, very limited molecular mechanism is available about how plants perceive and defend themselves from the destructive pest. Proteome technologies have provided an idea method for studying plant physiological processes in response to B. tabaci. RESULTS: Here, a highly resistant genotype and a highly susceptible genotype were exposed to B. tabaci feeding for 48 h to explore the defense mechanisms of pepper resistance to B. tabaci. The proteomic differences between both genotypes were compared using isobaric tag for relative and absolute quantification (iTRAQ). The quantitative data were validated by parallel reaction monitoring (PRM). The results showed that 37 differential abundance proteins (DAPs) were identified in the RG (resistant genotype), while 17 DAPs were identified in the SG (susceptible genotype) at 48 h after B. tabaci feeding. 77 DAPs were identified when comparing RG with SG without feeding. The DAP functions were determined for the classification of the pathways, mainly involved in redox regulation, stress response, protein metabolism, lipid metabolism and carbon metabolism. Some candidate DAPs are closely related to B. tabaci resistance such as annexin D4-like (ANN4), calreticulin-3 (CRT3), heme-binding protein 2-like (HBP1), acidic endochitinase pcht28-like (PR3) and lipoxygenase 2 (LOX2). CONCLUSIONS: Taken together, this study indicates complex resistance-related events in B. tabaci interaction, provides novel insights into the molecular mechanism underlying the response of plant to B. tabaci, and identifies some candidate proteins against B. tabaci attack.