School of Chemical Engineering and Technology, Tianjin University, Tianjin, 300072, People's Republic of China.
Appl Microbiol Biotechnol. 2013 Sep;97(18):8253-64. doi: 10.1007/s00253-013-5139-8. Epub 2013 Aug 8.
Salt stress is a common stress that limits growth and productivity of photosynthetic microbes in natural environments. Although cellular responses of a model cyanobacterium Synechocystis sp. PCC6803 to high and changing salt concentration have been studied, it remains undefined of the gene components and their regulation in the long-term salt acclimation networks. In this study, we performed an integrated study coupling a quantitative iTRAQ-LC-MS/MS proteomics and a next-generation sequencing-based RNA-seq transcriptomics on Synechocystis under salt stress for an extended period of time. Comparative quantification of protein abundances led to the identification of 68 and 108 proteins differentially regulated by salt treatment at 24 and 48 h, respectively. RNA-seq transcriptomic analysis showed that genes involved in energy metabolism and protein synthesis, and genes encoding hypothetical proteins responded to salt stress in a phase-dependent pattern. Notably, a gene encoding CO2-uptake-related protein (CupA) and three genes encoding hypothetical proteins were induced significantly at either transcript or protein level after long-term salt stress. Gene knockout and comparative growth analysis demonstrated that these four genes were involved in salt tolerance in Synechocystis. In addition, a complementary proteome and transcriptome analysis showed that concordance between protein abundances and their corresponding mRNAs varied significantly between various gene-protein pairs, indicating divergent regulation of transcriptional and post-transcriptional processes during salt stress adaptation in Synechocystis. The study provided new insights on genes and regulatory mechanism involved in salt stress response in Synechocystis.
盐胁迫是限制光合微生物在自然环境中生长和生产力的常见胁迫。尽管已经研究了模式蓝藻集胞藻 PCC6803 对高盐和变化盐浓度的细胞反应,但长期盐适应网络中的基因组成及其调控仍未确定。在这项研究中,我们对盐胁迫下的集胞藻进行了一项整合研究,结合了定量 iTRAQ-LC-MS/MS 蛋白质组学和基于下一代测序的 RNA-seq 转录组学。蛋白质丰度的比较定量导致分别在 24 和 48 小时的盐处理下鉴定出 68 和 108 个差异调节的蛋白质。RNA-seq 转录组分析表明,与能量代谢和蛋白质合成相关的基因以及编码假设蛋白的基因以相位依赖的模式对盐胁迫作出响应。值得注意的是,在长期盐胁迫后,一个编码 CO2 摄取相关蛋白 (CupA) 的基因和三个编码假设蛋白的基因在转录或蛋白质水平上均显著诱导。基因敲除和比较生长分析表明,这四个基因参与集胞藻的耐盐性。此外,互补的蛋白质组和转录组分析表明,蛋白质丰度与其相应 mRNA 之间的一致性在各种基因-蛋白对之间差异很大,表明在集胞藻适应盐胁迫过程中,转录和转录后过程的调控存在分歧。该研究为集胞藻中盐胁迫反应涉及的基因和调控机制提供了新的见解。