单细胞转录组分析揭示了掠食性纤毛虫的基因组进化过程

IF 1.9 2区 生物学 Q4 MICROBIOLOGY European journal of protistology Pub Date : 2024-02-05 DOI:10.1016/j.ejop.2024.126062
Zhaorui Zhou , Chao Li , Qingxiang Yuan , Yong Chi , Yuqing Li , Ying Yan , Saleh A. Al-Farraj , Naomi A. Stover , Zigui Chen , Xiao Chen
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引用次数: 0

摘要

许多纤毛原生动物捕食其他大型微生物,包括其他原生动物和微小的元古宙。纤毛虫类 Litostomatea 既有捕食性物种,也有内共生物种。由于缺乏基因组数据,人们对纤毛虫捕食能力的进化仍然知之甚少。为了填补这一空白,我们利用单细胞测序技术获得了六种捕食性纤毛虫的转录组图谱,并研究了它们的转录组特征。结果表明(1)与非捕食性纤毛虫相比,捕食性纤毛虫扩大了与跨膜活动和反应性氧化应激反应途径相关的基因家族,这可能是快速收缩和伸展等细胞行为的结果;(2) 钙激活 BK 钾通道基因家族的扩大(该基因家族假定调节细胞收缩性)是 Litostomatea 类的一个古老的进化事件,这表明与捕食性纤毛虫的狩猎行为有关的新陈代谢重新布线;以及 (3) 在 litostomateans 中发现了三次全基因组复制(WGD)事件,与生物合成过程、跨膜活性和钙激活钾通道活性有关的基因在 WGD 事件中得以保留。此外,我们还探讨了 17 种纤毛虫(包括 8 种 litostomateans)之间的进化关系,为今后深入研究 Litostomatea 的系统发生组学提供了丰富的基础数据集。我们的综合分析表明,通过扩大基因家族和WGD事件重新连接细胞代谢可能是猛禽纤毛虫捕食能力的潜在遗传基础。
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Single-cell transcriptomic analysis reveals genome evolution in predatory litostomatean ciliates

Many ciliated protists prey on other large microbial organisms, including other protists and microscopic metazoans. The ciliate class Litostomatea unites both predatory and endosymbiotic species. The evolution of predation ability in ciliates remains poorly understood, in part, due to a lack of genomic data. To fill this gap, we acquired the transcriptome profiles of six predatory litostomateans using single-cell sequencing technology and investigated their transcriptomic features. Our results show that: (1) in contrast to non-predatory ciliates, the predatory litostomateans have expanded gene families associated with transmembrane activity and reactive oxidative stress response pathways, potentially as a result of cellular behaviors such as fast contraction and extension; (2) the expansion of the calcium-activated BK potassium channel gene family, which hypothetically regulates cell contractility, is an ancient evolutionary event for the class Litostomatea, suggesting a rewired metabolism associated with the hunting behavior of predatory ciliates; and (3) three whole genome duplication (WGD) events have been detected in litostomateans, with genes associated with biosynthetic processes, transmembrane activity, and calcium-activated potassium channel activity being retained during the WGD events. In addition, we explored the evolutionary relationships among 17 ciliate species, including eight litostomateans, and provided a rich foundational dataset for future in-depth phylogenomic studies of Litostomatea. Our comprehensive analyses suggest that the rewired cellular metabolism via expanded gene families and WGD events might be the potential genetic basis for the predation ability of raptorial ciliates.

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来源期刊
European journal of protistology
European journal of protistology 生物-微生物学
CiteScore
4.60
自引率
20.70%
发文量
55
审稿时长
14.6 weeks
期刊介绍: Articles deal with protists, unicellular organisms encountered free-living in various habitats or as parasites or used in basic research or applications. The European Journal of Protistology covers topics such as the structure and systematics of protists, their development, ecology, molecular biology and physiology. Beside publishing original articles the journal offers a forum for announcing scientific meetings. Reviews of recently published books are included as well. With its diversity of topics, the European Journal of Protistology is an essential source of information for every active protistologist and for biologists of various fields.
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