State Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering, Southeast University, Nanjing 210096, China.
R&D Department, Singleron Biotechnology co., LTD, Nanjing 211800, China.
Genomics. 2020 Nov;112(6):5305-5312. doi: 10.1016/j.ygeno.2020.10.019. Epub 2020 Oct 20.
Zooxanthellae and coral can form an intracellular symbiotic system. Yet, little is known about the molecular mechanism underlying this symbiosis. In this study, we characterized the symbiosis based on analyses of gene expression at the single-cell level. Among 9110 single coral cells, we identified 4871 symbiotic cells based on the detection of both coral and zooxanthellae gene transcripts within a single cell. Using the bioinformatics tool Seurat, symbiotic cells were further clustered into five groups, 52 genes exhibited differential expression between groups. We proposed an index called the "symbiosis index", to indicate the degree of gene expression of both species in a single symbiotic cell. Interestingly, the index differed distinctly among the five groups. The symbiosis index was highly correlated with the expression of the coral gene gfas1.m1.6761 (ANKRD40), which encodes ankyrin repeat domain-containing protein 40 and is involved in DNA replication (r = 0.76). Two metabolism-related genes, DAGLA and betaGlu, were highly expressed in cells with a high symbiosis index. Four zooxanthellae genes, PRPF19, ATRN, aAA-ATPases and AK812-SmicGene44833, exhibited substantial changes in expression levels when zooxanthellae lived within coral. A trajectory analysis suggested that cells with a higher symbiosis index may be derived from those with a lower index during coral colony development. Taken together, our results provide evidence for zooxanthellae residing within coral, forming a symbiotic system. The symbiosis index is an effective indicator of different cell groups, with lineage relationships among groups. Additionally, we identified specific genes that exhibit expression changes in the symbiotic system.
共生藻和珊瑚可以形成细胞内共生系统。然而,对于这种共生关系的分子机制知之甚少。在这项研究中,我们基于单细胞水平的基因表达分析来描述共生关系。在 9110 个珊瑚单细胞中,我们根据单个细胞中珊瑚和共生藻基因转录本的检测,鉴定了 4871 个共生细胞。使用生物信息学工具 Seurat,将共生细胞进一步聚类为五个组,其中 52 个基因在组间表现出差异表达。我们提出了一个称为“共生指数”的指标,用于表示单个共生细胞中两种物种的基因表达程度。有趣的是,该指数在五个组之间明显不同。共生指数与珊瑚基因 gfas1.m1.6761(ANKRD40)的表达高度相关,该基因编码锚蛋白重复域蛋白 40,参与 DNA 复制(r=0.76)。两个代谢相关基因 DAGLA 和 betaGlu 在具有高共生指数的细胞中高度表达。四个共生藻基因 PRPF19、ATR、aAA-ATPases 和 AK812-SmicGene44833 的表达水平在共生藻存在于珊瑚内时发生了显著变化。轨迹分析表明,具有更高共生指数的细胞可能在珊瑚虫群体发育过程中来源于具有较低指数的细胞。综上所述,我们的结果为共生藻在珊瑚内定居并形成共生系统提供了证据。共生指数是不同细胞群的有效指标,具有群间的谱系关系。此外,我们还鉴定了在共生系统中表现出表达变化的特定基因。