Laboratory of Marine Protozoan Biodiversity and Evolution, Marine College, Shandong University, Weihai, 264209, China.
Department of Biology, Bradley University, Peoria, 61625, USA.
BMC Biol. 2024 Oct 15;22(1):237. doi: 10.1186/s12915-024-02026-5.
As a potential model organism for studies of environmental and cell biology, Paramecium duboscqui is a special euryhaline species of Paramecium that can be found in fresh, brackish, or marine water in natural salinity ranges between 0‰ and 33‰. However, the genome information as well as molecular mechanisms that account for its remarkable halotolerant traits remain extremely unknown. To characterize its genome feature, we combined PacBio and Illumina sequencing to assemble the first high-quality and near-complete macronuclear genome of P. duboscqui. Meanwhile, comparative transcriptomic profiles under different salinities gave underlying insight into the molecular mechanism of its adaptations to environmental salinity.
The results showed that the MAC genome of P. duboscqui comprises 160 contigs, with 113 of them possessing telomere (~ 28.82 Mb haploid genome size). Through comparative genomic analyses with the other ciliate, we found that gene families encoding transmembrane transporter proteins have been expanded in P. duboscqui, showing enormous potential in salinity adaptation. Like other Paramecium, P. duboscqui utilizes TGA as its only termination codon and has reassigned TAA and TAG to encode glutamine. P. duboscqui showed different growth rates under different salinities, with an optimum growth rate in 5‰ salinity. A comparison of the transcriptomic profiles among P. duboscqui grown under different concentrations showed that genes involved in protein folding, oxygen respiration, and glutathione-dependent detoxification were upregulated in the high-salt group, whereas genes encoding DNA-binding proteins and transcription factors were upregulated in the low-salt group, suggesting distinct mechanisms for responding to low and high salinity. Weighted gene coexpression network analysis (WGCNA) linked the hub genes expressed at 30‰ salinity to cysteine-type peptidase activity, lipid transfer, sodium hydrogen exchange, and cell division, with the hub genes expressed at 0‰ salinity involved in transmembrane transport and protein localization.
This study characterizes a new euryhaline model Paramecium, provides novel insights into Paramecium evolution, and describes the molecular mechanisms that have allow P. duboscqui to adapt to different osmotic environments.
作为环境和细胞生物学研究的潜在模式生物,杜氏草履虫是一种特殊的广盐性草履虫,可在淡水、半咸水或海洋水中生存,其自然盐度范围为 0‰ 至 33‰。然而,其基因组信息以及解释其显著耐盐特性的分子机制仍知之甚少。为了描述其基因组特征,我们结合 PacBio 和 Illumina 测序,组装了第一个高质量且近乎完整的杜氏草履虫大核基因组。同时,不同盐度下的比较转录组图谱为其适应环境盐度的分子机制提供了深入的了解。
结果表明,杜氏草履虫的 MAC 基因组由 160 个 contigs 组成,其中 113 个带有端粒(约 28.82 Mb 单倍体基因组大小)。通过与其他纤毛虫的比较基因组分析,我们发现编码跨膜转运蛋白的基因家族在杜氏草履虫中得到了扩展,显示出在盐分适应方面的巨大潜力。与其他草履虫一样,杜氏草履虫仅使用 TGA 作为其终止密码子,并将 TAA 和 TAG 重新分配来编码谷氨酰胺。杜氏草履虫在不同盐度下的生长速度不同,在 5‰盐度下生长速度最快。比较不同盐度下杜氏草履虫的转录组图谱表明,参与蛋白质折叠、氧气呼吸和谷胱甘肽依赖解毒的基因在高盐组中上调,而编码 DNA 结合蛋白和转录因子的基因在低盐组中上调,表明其对低盐和高盐的响应存在不同的机制。加权基因共表达网络分析(WGCNA)将在 30‰盐度下表达的枢纽基因与半胱氨酸型肽酶活性、脂质转移、钠氢交换和细胞分裂联系起来,而在 0‰盐度下表达的枢纽基因则与跨膜转运和蛋白质定位有关。
本研究描述了一种新的广盐性模式生物草履虫,为草履虫进化提供了新的见解,并描述了允许杜氏草履虫适应不同渗透环境的分子机制。