Single-cell transcriptomic analysis reveals genome evolution in predatory litostomatean ciliates

生物 纤毛的 转录组 捕食 进化生物学 基因组 草履虫 生态学 遗传学 基因 细胞生物学 基因表达
作者
Zhaorui Zhou,Chao Li,Qingxiang Yuan,Yong Chi,Yuqing Li,Ying Yan,Saleh Alfarraj,Naomi A. Stover,Zigui Chen,Xiao Chen
出处
期刊:European Journal of Protistology [Elsevier BV]
卷期号:93: 126062-126062
标识
DOI:10.1016/j.ejop.2024.126062
摘要

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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