De novo RNA sequencing analysis of Aeluropus littoralis halophyte plant under salinity stress

The study of salt tolerance mechanisms in halophyte plants can provide valuable information for crop breeding and plant engineering programs. The aim of the present study was to investigate whole transcriptome analysis of Aeluropus littoralis in response to salinity stress (200 and 400mM NaCl) by de novo RNA-sequencing. To assemble the transcriptome, Trinity v2.4.0 and Bridger tools, were comparatively used with two k-mer sizes (25 and 32bp). The de novo assembled transcriptome by Bridger (k-mer 32) was chosen as final assembly for subsequent analysis. In general, 103290 transcripts were obtained. The differential expression analysis (log(2)(FC)>1 and FDR<0.01) showed that 1861 transcripts expressed differentially, including169 up and 316 down-regulated transcripts in 200mM NaCl treatment and 1035 up and 430 down-regulated transcripts in 400mM NaCl treatment compared to control. In addition, 89 transcripts were common in both treatments. The most important over-represented terms in the GO analysis of differentially expressed genes (FDR<0.05) were chitin response, response to abscisic acid, and regulation of jasmonic acid mediated signaling pathway under 400mM NaCl treatment and cell cycle, cell division, and mitotic cell cycle process under 200mM treatment. In addition, the phosphatidylcholine biosynthetic process term was common in both salt treatments. Interestingly, under 400mM salt treatment, the PRC1 complex that contributes to chromatin remodeling was also enriched along with vacuole as a general salinity stress responsive cell component. Among enriched pathways, the MAPK signaling pathway (ko04016) and phytohormone signal transduction (ko04075) were significantly enriched in 400mM NaCl treatment, whereas DNA replication (ko03032) was the only pathway that significantly enriched in 200mM NaCl treatment. Finally, our findings indicate the salt-concentration depended responses of A. littoralis, which well-known salinity stress-related pathways are induced in 400mM NaCl, while less considered pathways, e.g. cell cycle and DNA replication, are highlighted under 200mM NaCl treatment.