Group-specific functional patterns of mitochondrion-related organelles shed light on their multiple transitions from mitochondria in ciliated protists.

IF 5.8 2区 生物学 Q1 MARINE & FRESHWATER BIOLOGY Marine Life Science & Technology Pub Date : 2022-11-21 eCollection Date: 2022-11-01 DOI:10.1007/s42995-022-00147-w
Zhicheng Chen, Jia Li, Dayana E Salas-Leiva, Miaoying Chen, Shilong Chen, Senru Li, Yanyan Wu, Zhenzhen Yi
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引用次数: 0

Abstract

Adaptations of ciliates to hypoxic environments have arisen independently several times. Studies on mitochondrion-related organelle (MRO) metabolisms from distinct anaerobic ciliate groups provide evidence for understanding the transitions from mitochondria to MROs within eukaryotes. To deepen our knowledge about the evolutionary patterns of ciliate anaerobiosis, mass-culture and single-cell transcriptomes of two anaerobic species, Metopus laminarius (class Armophorea) and Plagiopyla cf. narasimhamurtii (class Plagiopylea), were sequenced and their MRO metabolic maps were compared. In addition, we carried out comparisons using publicly available predicted MRO proteomes from other ciliate classes (i.e., Armophorea, Litostomatea, Muranotrichea, Oligohymenophorea, Parablepharismea and Plagiopylea). We found that single-cell transcriptomes were similarly comparable to their mass-culture counterparts in predicting MRO metabolic pathways of ciliates. The patterns of the components of the MRO metabolic pathways might be divergent among anaerobic ciliates, even among closely related species. Notably, our findings indicate the existence of group-specific functional relics of electron transport chains (ETCs). Detailed group-specific ETC functional patterns are as follows: full oxidative phosphorylation in Oligohymenophorea and Muranotrichea; only electron-transfer machinery in Armophorea; either of these functional types in Parablepharismea; and ETC functional absence in Litostomatea and Plagiopylea. These findings suggest that adaptation of ciliates to anaerobic conditions is group-specific and has occurred multiple times. Our results also show the potential and the limitations of detecting ciliate MRO proteins using single-cell transcriptomes and improve the understanding of the multiple transitions from mitochondria to MROs within ciliates.

Supplementary information: The online version contains supplementary material available at 10.1007/s42995-022-00147-w.

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线粒体相关细胞器的群体特异性功能模式揭示了纤毛原生生物线粒体的多重转变。
纤毛虫对低氧环境的适应已经独立出现了好几次。对不同厌氧纤毛虫群线粒体相关细胞器(MRO)代谢的研究为理解真核生物从线粒体到MRO的转变提供了证据。为了加深对纤毛虫厌氧进化模式的认识,我们对两种厌氧物种Metopus laminarius (Armophorea纲)和Plagiopyla cf. narasimhamurtii (Plagiopylea纲)进行了大规模培养和单细胞转录组测序,并比较了它们的MRO代谢图谱。此外,我们还利用其他纤毛虫类(即Armophorea, Litostomatea, Muranotrichea, oligohymenopause, parable法利亚法利亚和Plagiopylea)的公开预测MRO蛋白质组进行了比较。我们发现单细胞转录组在预测纤毛虫的MRO代谢途径方面与大众培养的转录组相似。在厌氧纤毛虫之间,甚至在密切相关的物种之间,MRO代谢途径的组分模式可能是不同的。值得注意的是,我们的发现表明电子传递链(ETCs)存在基团特异性功能遗迹。详细的组特异性ETC功能模式如下:寡膜蜂和Muranotrichea的完全氧化磷酸化;Armophorea中只有电子转移机械;比喻法利赛mea中的这两种功能类型;垂口目和斜翼目ETC功能缺失。这些发现表明,纤毛虫对厌氧条件的适应是群体特异性的,并且已经发生过多次。我们的研究结果还显示了利用单细胞转录组检测纤毛虫MRO蛋白的潜力和局限性,并提高了对纤毛虫从线粒体到MRO的多重转变的理解。补充信息:在线版本包含补充资料,下载地址:10.1007/s42995-022-00147-w。
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来源期刊
Marine Life Science & Technology
Marine Life Science & Technology MARINE & FRESHWATER BIOLOGY-
CiteScore
9.60
自引率
10.50%
发文量
58
期刊介绍: Marine Life Science & Technology (MLST), established in 2019, is dedicated to publishing original research papers that unveil new discoveries and theories spanning a wide spectrum of life sciences and technologies. This includes fundamental biology, fisheries science and technology, medicinal bioresources, food science, biotechnology, ecology, and environmental biology, with a particular focus on marine habitats. The journal is committed to nurturing synergistic interactions among these diverse disciplines, striving to advance multidisciplinary approaches within the scientific field. It caters to a readership comprising biological scientists, aquaculture researchers, marine technologists, biological oceanographers, and ecologists.
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