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The m6A pathway protects the transcriptome integrity by restricting RNA chimera formation in plants

机译:m6A途径通过限制植物中RNA嵌合体的形成来保护转录组的完整性

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摘要

Global, segmental, and gene duplication–related processes are driving genome size and complexity in plants. Despite their evolutionary potentials, those processes can also have adverse effects on genome regulation, thus implying the existence of specialized corrective mechanisms. Here, we report that an N6-methyladenosine (m6A)–assisted polyadenylation (m-ASP) pathway ensures transcriptome integrity in Arabidopsis thaliana. Efficient m-ASP pathway activity requires the m6A methyltransferase-associated factor FIP37 and CPSF30L, an m6A reader corresponding to an YT512-B Homology Domain-containing protein (YTHDC)-type domain containing isoform of the 30-kD subunit of cleavage and polyadenylation specificity factor. Targets of the m-ASP pathway are enriched in recently rearranged gene pairs, displayed an atypical chromatin signature, and showed transcriptional readthrough and mRNA chimera formation in FIP37- and CPSF30L-deficient plants. Furthermore, we showed that the m-ASP pathway can also restrict the formation of chimeric gene/transposable-element transcript, suggesting a possible implication of this pathway in the control of transposable elements at specific locus. Taken together, our results point to selective recognition of 3′-UTR m6A as a safeguard mechanism ensuring transcriptome integrity at rearranged genomic loci in plants.
机译:全局,分段和基因复制相关的过程正在驱动植物的基因组大小和复杂性。尽管具有进化潜力,但这些过程也可能对基因组调控产生不利影响,因此暗示存在专门的校正机制。在这里,我们报道了N6-甲基腺苷(m 6 A)辅助的聚腺苷酸化(m-ASP)途径可确保拟南芥中转录组的完整性。有效的m-ASP途径活性需要m 6 A甲基转移酶相关因子FIP37和CPSF30L,即与YT512-B同源结构域蛋白相对应的m 6 A阅读器( YTHDC)型结构域,包含30-kD裂解亚基和聚腺苷酸特异性因子的亚型。 m-ASP途径的靶标富含最近重新排列的基因对,在FIP37和CPSF30L缺陷型植物中表现出非典型的染色质特征,并显示转录通读和mRNA嵌合体形成。此外,我们表明,m-ASP途径还可以限制嵌合基因/转座因子转录物的形成,表明该途径可能在特定位点控制转座因子。综上所述,我们的结果表明选择性识别3'-UTR m 6 A是一种保护机制,可确保植物基因组重排时转录组的完整性。

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