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从 Oikopleura dioica 的线粒体基因组看进化:测序挑战、RNA 编辑、基因向核转移和 tRNA 丢失。

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

机构信息

George S. Wise Faculty of Life Sciences, School of Zoology, Tel Aviv University, Tel Aviv 6997801, Israel.

Faculty of Health and Medical Sciences, GeoGenetics Centre, GLOBE Institute, University of Copenhagen, Copenhagen, Denmark.

出版信息

Genome Biol Evol. 2024 Sep 3;16(9). doi: 10.1093/gbe/evae181.

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.

摘要

由于长的聚 A/T 同源多聚物序列的存在,使得测序和组装变得具有挑战性,因此对被囊动物 Oikopleura dioica 的线粒体基因组进行测序是一项具有挑战性的任务。在这里,我们通过结合 Illumina 和 MinIon Oxford Nanopore 技术获得的多个 DNA 和扩增子读数以及公共 RNA 序列,报告了 O. dioica 的线粒体基因组的大部分测序和注释。我们记录了广泛的 RNA 编辑,因为线粒体 DNA 中存在的所有同源多聚物序列都对应于线粒体 RNA 中的 6U 区域。在 13 个典型的蛋白质编码基因中,我们能够检测到 8 个,加上一个没有与典型线粒体蛋白质编码基因序列相似性的未分配的开放阅读框。我们表明 nad3 基因已转移到细胞核并获得了线粒体靶向信号。除了两个非常短的 rRNA 外,我们只能识别出单个 tRNA(tRNA-Met),这表明多个 tRNA 基因丢失,这得到了核基因组中相应的线粒体氨酰-tRNA 合成酶丢失的支持。基于鉴定出的 8 个典型蛋白质编码基因,我们重建了最大似然和贝叶斯系统发育树,并推断出这个线粒体基因组的极端进化率。然而,被囊动物中环节动物的系统发育位置仍无法准确确定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b1f/11384887/292df2921492/evae181f1.jpg

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