拟南芥热诱导转录转座子的自然多样性

IF 3.2 2区 生物学 Q2 EVOLUTIONARY BIOLOGY
Wenbo Xu, Michael Thieme, Anne C Roulin
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引用次数: 0

摘要

可转座元件(Transposable elements,TEs)是植物基因组的主要组成部分,对宿主的适应性有深远影响。然而,技术瓶颈长期以来一直阻碍着我们对可转座元件的机理认识。我们利用牛津纳米孔技术公司(ONT)的直接 cDNA 测序技术进行了 RNA-Seq 和长序列测序,分析了拟南芥三个天然品种(Cvi-0、Col-0 和 Ler-1)中热诱导的 TEs 转录。除了研究较多的ONSEN逆转录质子家族外,我们还证实了Copia-35是第二个热响应逆转录质子家族,在孑遗种Cvi-0中具有特别高的活性。我们的分析揭示了单个TE拷贝的不同表达模式,并表明在ONSEN和Copia-35家族中存在不同的GAG蛋白生产调控机制。此外,与 ONSEN 类似,Copia-35 的激活也导致了侧翼基因(如 AMUP9)的上调,并可能导致花期的定量调节。通过 ONT 数据,我们可以检验通读形成在多大程度上对相邻基因的调控起着重要作用。意想不到的是,我们的结果表明,对于这两个家族来说,侧翼基因的上调并不主要是由其 3' LTR 的转录直接启动的。这些发现凸显了在胁迫下与逆转录质子激活相关的种内表达多样性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Natural Diversity of Heat-Induced Transcription of Retrotransposons in Arabidopsis thaliana.

Transposable elements (TEs) are major components of plant genomes, profoundly impacting the fitness of their hosts. However, technical bottlenecks have long hindered our mechanistic understanding of TEs. Using RNA-Seq and long-read sequencing with Oxford Nanopore Technologies' (ONT) direct cDNA sequencing, we analyzed the heat-induced transcription of TEs in three natural accessions of Arabidopsis thaliana (Cvi-0, Col-0, and Ler-1). In addition to the well-studied ONSEN retrotransposon family, we confirmed Copia-35 as a second heat-responsive retrotransposon family with particularly high activity in the relict accession Cvi-0. Our analysis revealed distinct expression patterns of individual TE copies and suggest different mechanisms regulating the GAG protein production in the ONSEN versus Copia-35 families. In addition, analogously to ONSEN, Copia-35 activation led to the upregulation of flanking genes such as APUM9 and potentially to the quantitative modulation of flowering time. ONT data allowed us to test the extent to which read-through formation is important in the regulation of adjacent genes. Unexpectedly, our results indicate that for both families, the upregulation of flanking genes is not predominantly directly initiated by transcription from their 3' long terminal repeats. These findings highlight the intraspecific expressional diversity linked to retrotransposon activation under stress.

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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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