可进行 RNAi 内共生的模式系统鹦鹉螺 186b 的全新基因组序列组装揭示了影响内含子谱系的因素

Guy Leonard, Benjamin H Jenkins, Fiona R Savory, Estelle S Kilias, Finlay Maguire, Varun Varma, David S Milner, Thomas A Richards
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引用次数: 0

摘要

两个物种如何进行稳定的内共生是一个生物学难题。对兼性内共生相互作用的研究已成为了解内共生功能如何产生的一种有用方法。纤毛虫类原生动物法氏囊河马寄主于绿藻纲的绿藻,进行兼性光内共生。我们最近报告了 RNAi 作为一种了解法氏副纤毛虫 186b(CCAP 1660/18 株)基因功能的工具 [1]。为了补充这项工作,我们在此报告了一个高度完整的宿主基因组和转录组序列数据集,使用 Illumina 和 PacBio 两种测序方法帮助进行基因组分析,并设计 RNAi 实验。我们的分析表明,法氏囊伞菌与其他纤毛虫(如各种伞菌)一样,拥有大量微小的内含子。这些数据与纤毛虫常见的另类遗传密码相结合,使得基因鉴定和注释工作充满挑战。为了进一步探索内含子的进化动态,我们发现在数量较少的长内含子中,导致内含子保留的替代剪接发生频率较高,从而确定了针对长内含子的选择源。这些数据将有助于研究鹦鹉螺的基因组进化,并为探索内共生功能提供更多的源数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
De novo genome sequence assembly of the RNAi-tractable endosymbiosis model system Paramecium bursaria 186b reveals factors shaping intron repertoire
How two species engage in stable endosymbiosis is a biological quandary. The study of facultative endosymbiotic interactions has emerged as a useful approach to understand how endosymbiotic functions can arise. The ciliate protist Paramecium bursaria hosts green algae of the order Chlorellales in a facultative photo-endosymbiosis. We have recently reported RNAi as a tool for understanding gene function in Paramecium bursaria 186b, CCAP strain 1660/18 [1]. To complement this work, here we report a highly complete host genome and transcriptome sequence dataset, using both Illumina and PacBio sequencing methods to aid genome analysis and to enable the design of RNAi experiments. Our analyses demonstrate Paramecium bursaria, like other ciliates such as diverse species of Paramecia, possess numerous tiny introns. These data, combined with the alternative genetic code common to ciliates, makes gene identification and annotation challenging. To explore intron evolutionary dynamics further we show that alternative splicing leading to intron retention occurs at a higher frequency among the smaller number of longer introns, identifying a source of selection against longer introns. These data will aid the investigation of genome evolution in the Paramecia and provide additional source data for the exploration of endosymbiotic functions.
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