Jilin Provincial Key Laboratory of Plant Resource Science and Green Production, Jilin Normal University, Siping, Jilin Province, China.
PLoS One. 2021 Mar 4;16(3):e0248155. doi: 10.1371/journal.pone.0248155. eCollection 2021.
Nitrogen assimilation is strictly regulated in cyanobacteria. In an inorganic nitrogen-deficient environment, some vegetative cells of the cyanobacterium Anabaena differentiate into heterocysts. We assessed the photosynthesis and nitrogen-fixing capacities of heterocysts and vegetative cells, respectively, at the transcriptome level. RNA extracted from nitrogen-replete vegetative cells (NVs), nitrogen-deprived vegetative cells (NDVs), and nitrogen-deprived heterocysts (NDHs) in Anabaena sp. strain PCC 7120 was evaluated by transcriptome sequencing. Paired comparisons of NVs vs. NDHs, NVs vs. NDVs, and NDVs vs. NDHs revealed 2,044 differentially expressed genes (DEGs). Kyoto Encyclopedia of Genes and Genomes enrichment analysis of the DEGs showed that carbon fixation in photosynthetic organisms and several nitrogen metabolism-related pathways were significantly enriched. Synthesis of Gvp (Gas vesicle synthesis protein gene) in NVs was blocked by nitrogen deprivation, which may cause Anabaena cells to sink and promote nitrogen fixation under anaerobic conditions; in contrast, heterocysts may perform photosynthesis under nitrogen deprivation conditions, whereas the nitrogen fixation capability of vegetative cells was promoted by nitrogen deprivation. Immunofluorescence analysis of nitrogenase iron protein suggested that the nitrogen fixation capability of vegetative cells was promoted by nitrogen deprivation. Our findings provide insight into the molecular mechanisms underlying nitrogen fixation and photosynthesis in vegetative cells and heterocysts at the transcriptome level. This study provides a foundation for further functional verification of heterocyst growth, differentiation, and water bloom control.
氮同化在蓝细菌中受到严格调控。在无机氮缺乏的环境中,某些蓝细菌鱼腥藻的营养细胞分化为异形胞。我们分别在转录组水平上评估了异形胞和营养细胞的光合作用和固氮能力。从鱼腥藻 PCC 7120 的氮充足营养细胞 (NVs)、氮饥饿营养细胞 (NDVs) 和氮饥饿异形胞 (NDHs) 中提取的 RNA 通过转录组测序进行评估。NVs 与 NDHs、NVs 与 NDVs 和 NDVs 与 NDHs 的成对比较揭示了 2044 个差异表达基因 (DEGs)。DEGs 的京都基因与基因组百科全书富集分析表明,光合生物的碳固定和几种氮代谢相关途径显著富集。氮饥饿阻断了 NVs 中 Gvp(气胞合成蛋白基因)的合成,这可能导致鱼腥藻细胞下沉,并在厌氧条件下促进固氮;相比之下,异形胞可能在氮饥饿条件下进行光合作用,而营养细胞的固氮能力则受到氮饥饿的促进。氮酶铁蛋白的免疫荧光分析表明,氮饥饿促进了营养细胞的固氮能力。我们的研究结果为在转录组水平上了解营养细胞和异形胞固氮和光合作用的分子机制提供了线索。这项研究为进一步验证异形胞生长、分化和水华控制的功能提供了基础。