单核海绵B支(Porifera, Demospongiae)线粒体tRNA基因普遍缺失。

IF 3.2 2区 生物学 Q2 EVOLUTIONARY BIOLOGY
Dennis V Lavrov, Thomas L Turner, Jan Vicente
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引用次数: 0

摘要

线粒体tRNA基因丢失和胞质tRNA输入是线粒体生物学中的两种常见现象,但它们在动物中的重要性往往被低估。这是因为大多数双侧对称动物(Bilateria)的线粒体DNA (mtDNA)编码线粒体翻译所需的一整套trna。相比之下,非双边动物(刺胞门、栉虫门、Porifera门和Placozoa门)的mtDNA通常含有一组减少的tRNA基因,需要从细胞质中输入tRNA。有趣的是,在许多非双边谱系中,tRNA基因含量似乎在进化早期就已确定,此后一直保持保守。在这里,我们报告了单轴海绵(CBHS)的B支是这种模式的一个例外,即使在相对密切相关的物种中,tRNA基因含量也表现出相当大的差异。我们确定了8个CBHS物种的mt-基因组序列,并将它们与6个先前可用的序列相结合进行了分析。此外,我们对CBHS外的两种单体型海绵进行了mt-基因组测序,并使用了8个先前可用的序列作为外群。我们发现,在CBHS中,tRNA基因含量差异很大,从一个未描述的Haliclona物种(Haliclona sp. TLT785)的3个到Xestospongia muta和X. testudinaria的25个。此外,我们发现除Xestospongia属外的所有CBHS物种都缺乏atp9基因,其中一些也缺乏atp8基因。对洋地黄Niphates核序列的分析显示,atp8和atp9都转移到了核基因组中,而mt-tRNA基因的缺失表明它们真正丢失了。我们认为CBHS可以作为一个有价值的系统来研究mt-tRNA基因丢失、细胞质trna的线粒体输入以及这些过程对线粒体进化的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pervasive Mitochondrial tRNA Gene Loss in Clade B of Haplosclerid Sponges (Porifera, Demospongiae).

Mitochondrial tRNA gene loss and cytosolic tRNA import are two common phenomena in mitochondrial biology, but their importance is often under-appreciated in animals. This is because the mitochondrial DNA (mtDNA) of most bilaterally symmetrical animals (Bilateria) encodes a complete set of tRNAs required for mitochondrial translation. By contrast, the mtDNA of nonbilaterian animals (phyla Cnidaria, Ctenophora, Porifera, and Placozoa) often contains a reduced set of tRNA genes, necessitating tRNA import from the cytosol. Interestingly, in many nonbilaterian lineages, tRNA gene content appears to be set early in evolution and remains conserved thereafter. Here, we report that Clade B of haplosclerid sponges (CBHS) represents an exception to this pattern, displaying considerable variation in tRNA gene content even among relatively closely related species. We determined mt-genome sequences for eight CBHS species and analyzed them in conjunction with six previously available sequences. Additionally, we sequenced mt-genomes for two species of haplosclerid sponges outside the CBHS and used them with eight previously available sequences as outgroups. We found that tRNA gene content varied widely within CBHS, ranging from three in an undescribed Haliclona species (Haliclona sp. TLT785) to 25 in Xestospongia muta and X. testudinaria. Furthermore, we found that all CBHS species outside the genus Xestospongia lacked the atp9 gene, with some also lacking atp8. Analysis of nuclear sequences from Niphates digitalis revealed that both atp8 and atp9 had transferred to the nuclear genome, while the absence of mt-tRNA genes indicated their genuine loss. We argue that CBHS can serve as a valuable system for studying mt-tRNA gene loss, mitochondrial import of cytosolic tRNAs, and the impact of these processes on mitochondrial evolution.

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来源期刊
Genome Biology and Evolution
Genome Biology and Evolution EVOLUTIONARY BIOLOGY-GENETICS & HEREDITY
CiteScore
5.80
自引率
6.10%
发文量
169
审稿时长
1 months
期刊介绍: About the journal Genome Biology and Evolution (GBE) publishes leading original research at the interface between evolutionary biology and genomics. Papers considered for publication report novel evolutionary findings that concern natural genome diversity, population genomics, the structure, function, organisation and expression of genomes, comparative genomics, proteomics, and environmental genomic interactions. Major evolutionary insights from the fields of computational biology, structural biology, developmental biology, and cell biology are also considered, as are theoretical advances in the field of genome evolution. GBE’s scope embraces genome-wide evolutionary investigations at all taxonomic levels and for all forms of life — within populations or across domains. Its aims are to further the understanding of genomes in their evolutionary context and further the understanding of evolution from a genome-wide perspective.
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