Evolutionary Insights from the Mitochondrial Genome of Oikopleura dioica: Sequencing Challenges, RNA Editing, Gene Transfers to the Nucleus, and tRNA Loss.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Yael Klirs, Maria Novosolov, Carmela Gissi, Rade Garić, Tal Pupko, Thomas Stach, Dorothée Huchon
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Abstract

Sequencing the mitochondrial genome of the tunicate Oikopleura dioica is a challenging task due to the presence of long poly-A/T homopolymer stretches, which impair sequencing and assembly. Here, we report on the sequencing and annotation of the majority of the mitochondrial genome of O. dioica by means of combining several DNA and amplicon reads obtained by Illumina and MinIon Oxford Nanopore Technologies with public RNA sequences. We document extensive RNA editing, since all homopolymer stretches present in the mitochondrial DNA correspond to 6U-regions in the mitochondrial RNA. Out of the 13 canonical protein-coding genes, we were able to detect eight, plus an unassigned open reading frame that lacked sequence similarity to canonical mitochondrial protein-coding genes. We show that the nad3 gene has been transferred to the nucleus and acquired a mitochondria-targeting signal. In addition to two very short rRNAs, we could only identify a single tRNA (tRNA-Met), suggesting multiple losses of tRNA genes, supported by a corresponding loss of mitochondrial aminoacyl-tRNA synthetases in the nuclear genome. Based on the eight canonical protein-coding genes identified, we reconstructed maximum likelihood and Bayesian phylogenetic trees and inferred an extreme evolutionary rate of this mitochondrial genome. The phylogenetic position of appendicularians among tunicates, however, could not be accurately determined.

Oikopleura dioica 线粒体基因组的进化启示:测序挑战、RNA 编辑、基因转移到细胞核以及 tRNA 丢失。
对鳞栉水母线粒体基因组进行测序是一项极具挑战性的任务,因为其中存在长的多聚-A/T均聚物链段,影响测序和组装。在此,我们报告了通过将 Illumina 和 MinIon 牛津纳米孔技术公司(ONT)获得的 DNA 和扩增子读数与公开的 RNA 序列相结合,对 O. dioica 的大部分线粒体基因组进行测序和注释的情况。我们记录了广泛的 RNA 编辑,因为线粒体 DNA 中的所有同源多聚物链段都与线粒体 RNA 中的 6U 区域相对应。在 13 个标准蛋白编码基因中,我们能够检测到 8 个,另外还有一个未指定的 ORF,它与标准线粒体蛋白编码基因缺乏序列相似性。我们发现 nad3 基因已转移到细胞核中,并获得了线粒体靶向信号。除了两个非常短的 rRNA 外,我们只能鉴定出一个 tRNA(tRNA-Met),这表明有多个 tRNA 基因丢失,核基因组中的线粒体氨基酰-tRNA 合成酶也相应丢失。根据所发现的八个典型蛋白编码基因,我们重建了最大似然法和贝叶斯系统发生树,并推断出了该线粒体基因组的极端进化速度。然而,我们无法准确确定附肢动物在石龙子类中的系统发育位置。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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