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Transcriptomic and Proteomic analyses provide insights into the adaptive responses to the combined impact of salinity and alkalinity in Gymnocypris przewalskii

ABSTRACT: In this study, the DIA/SWATH method was used to identify differentially expressed proteins (DEPs) under saline, alkaline, and saline-alkaline stresses. Combined analyses of the proteome and transcriptome, pairwise differential abundance analysis, and gene regulated networks were implemented to identify key responsive GO items and KEGG pathways. Furthermore, proteins and cellular pathways related to the alkaline-saline effect were characterized, and some were validated through Western blotting. Finally, the relationship of stresses with homeostasis processes, immune responses, and reproductive processes is discussed. These results established a proteomics database of Gymnocypris przewalskii and should be helpful for understanding the physiological regulation mechanisms under salinity, alkalinity, and salinity-alkalinity interactive stresses.

ORGANISM(S): Gymnocypris Przewalskii

SUBMITTER: Jian Liang

PROVIDER: PXD033567 | iProX | Sat Apr 30 00:00:00 BST 2022

REPOSITORIES: iProX

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Project description:In low rainfall regions soils are naturally conditioned with frequent co-occurrence of salinity and alkalinity. Plant salinity responses both at physiological and molecular level have been extensively researched. However, effects of the combined treatment of alkaline salinity that could greatly reduce plant growth and the mechanisms responsible for tolerance remain indeterminate. In Brassica juncea, large reductions in biomass and increased leaf Na+ concentration under alkaline salinity indicates that the combined treatment had greater negative effect than salinity on both growth and the physiological responses of the plant. To determine molecular mechanisms potentially controlling adaptive tolerance responses to salinity and alkaline salinity, the moderately tolerant genotype NDR 8501 was further investigated using microarray analysis. The transcripts of treated leaf tissues verses those of the untreated control sample were analysed after prolonged stress of four weeks. In total, 528 salinity responsive and 1245 alkaline salinity responsive genes were indentified and only 101 genes were expressed jointly in either of the two treatments. Transcription of 37% more genes involved in response to alkaline salinity than salinity alone, which suggests the increased impact and severity of the combined stress on the plant, indicating the transcription of a far greater number of genes likely involved in mitigation and damage control. Transcription of KUP2 and KUP7 genes involved in potassium homeostasis under salinity alone and NHX1 and ENH1 genes for ion (K+ and Na+) homeostasis under alkaline salinity, clearly demonstrated that different genes and genetic pathways are involved in response to each stress. They further provide supporting evidence for the physiological responses that occur in the plant, with massive reprogramming of the transcriptome leading to partial ion exclusion, shuttling and compartmentation. Salinity and alkaline salinity induced gene expression in Brassica juncea leaf was measured at 4 weeks of prolonged treatment of 50 mM NaCl alone and combined with 2.5 mM HCO3- versus non-stressed control. A single experiment was conducted using Brassica juncea genotype NDR 8501 at a single time point (fours weeks after treatment) with three replications per treatment.

Project description:Sinonovacula constricta is an economically important bivalve species in China, Korea and Japan. It widely resides in estuarine and coastal areas where salinity fluctuates rapidly. However, little is known about its adaptation mechanisms to acute salt stresses. To address this, we establish nine cDNA libraries (triplicate each treatment) from juvenile S. constricta, which were subjected to low salinity (5 psu), optimal salinity (15 psu, the control) and high salinity (25 psu) for 6 h, respectively. Illumina sequencing generated 478,587,310 clean reads totally, which were assembled into 427,057 transcripts of 246,672 unigenes. Compared with the control, 1259 and 2163 differentially expressed genes (DEGs) were identified under acute low and high salt stresses, respectively. GO and KEGG enrichment analyses of DEGs suggested that several key metabolic modulations were mainly responsible for the acute salt stresses. Based on the significantly highlighted KEGG pathways, some key DEGs were identified and discussed in details, including cysteine sulfinic acid decarboxylase, alanine transaminase, glutamine synthetase, glutamate dehydrogenase, nitric-oxide synthase, arginase, betaine-homocysteine S-methyltransferase, serine racemase, L-serine ammonia-lyase, phosphoserine phosphatase, glutamate 5-kinase, glutamate-5-semialdehyde dehydrogenase, ornithine-oxo-acid transaminase, ornithine decarboxylase, stearoyl-CoA desaturase, carnitine O-palmitoyltransferase 1, serine/threonine-protein kinase, NF-kappa-B, NF-kappa-B inhibitor alpha, phosphoenolpyruvate carboxykinase and carbohydrate response element binding protein. Furthermore, some potential osmolytes were speculated. In summary, this study would not only provide insights into the adaptation mechanisms to acute salt stresses in juvenile S. constricta, but also facilitate to better understand the physical and biochemical performances of this bivalve species involved in acute salt stresses. Moreover, the transcriptome data obtained here greatly enriched the genetic information of S. constricta, which would be valuable for promoting its molecular biology researches.

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Transcriptomic and Proteomic analyses provide insights into the adaptive responses to the combined impact of salinity and alkalinity in Gymnocypris przewalskii

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