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首页> 外文期刊>Genes >Deep Transcriptome Sequencing of Two Green Algae, Chara vulgaris and Chlamydomonas reinhardtii , Provides No Evidence of Organellar RNA Editing
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Deep Transcriptome Sequencing of Two Green Algae, Chara vulgaris and Chlamydomonas reinhardtii , Provides No Evidence of Organellar RNA Editing

机译:两个绿藻,寻常型Chara和莱茵衣藻的深转录组测序,没有证据显示细胞器RNA的编辑

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Nearly all land plants post‐transcriptionally modify specific nucleotides within RNAs, a process known as RNA editing. This adaptation allows the correction of deleterious mutations within the asexually reproducing and presumably non‐recombinant chloroplast and mitochondrial genomes. There are no reports of RNA editing in any of the green algae so this phenomenon is presumed to have originated in embryophytes either after the invasion of land or in the now extinct algal ancestor of all land plants. This was challenged when a recent in silico screen for RNA edit sites based on genomic sequence homology predicted edit sites in the green alga Chara vulgaris, a multicellular alga found within the Streptophyta clade and one of the closest extant algal relatives of land plants. In this study, the organelle transcriptomes of C. vulgaris and Chlamydomonas reinhardtii were deep sequenced for a comprehensive assessment of RNA editing. Initial analyses based solely on sequence comparisons suggested potential edit sites in both species, but subsequent high‐resolution melt analysis, RNase H‐dependent PCR (rhPCR), and Sanger sequencing of DNA and complementary DNAs (cDNAs) from each of the putative edit sites revealed them to be either single‐nucleotide polymorphisms (SNPs) or spurious deep sequencing results. The lack of RNA editing in these two lineages is consistent with the current hypothesis that RNA editing evolved after embryophytes split from its ancestral algal lineage.
机译:几乎所有陆地植物在转录后都会修饰RNA中的特定核苷酸,这一过程称为RNA编辑。这种适应性可以校正无性繁殖且可能非重组的叶绿体和线粒体基因组中的有害突变。没有关于任何绿藻中RNA编辑的报道,因此推测该现象起源于入侵土地后或所有土地植物现已灭绝的藻类祖先的胚芽。当最近基于基因组序列同源性的计算机模拟筛选RNA编辑位点时,这挑战了绿藻Chara vulgaris(链霉菌属进化枝中发现的一种多细胞藻类,也是陆地植物现存最接近的藻类近亲之一)中的编辑位点。在这项研究中,对C. vulgaris和莱茵衣藻的细胞器转录组进行了深度测序,以对RNA编辑进行全面评估。仅基于序列比较的初步分析表明,这两个物种都有潜在的编辑位点,但随后的高分辨率熔解分析,RNase H依赖PCR(rhPCR)以及每个推定编辑位点的DNA和互补DNA(cDNA)的Sanger测序发现它们是单核苷酸多态性(SNP)或伪深测序结果。这两个谱系中缺少RNA编辑,这与当前的假设一致,即RNA编辑在胚胎植物从其祖先藻类谱系分裂后进化而来。

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