Department of Molecular Genetics, The Ohio State University, Columbus, Ohio, USA.
PLoS Genet. 2012 Feb;8(2):e1002474. doi: 10.1371/journal.pgen.1002474. Epub 2012 Feb 9.
The epigenetic activity of transposable elements (TEs) can influence the regulation of genes; though, this regulation is confined to the genes, promoters, and enhancers that neighbor the TE. This local cis regulation of genes therefore limits the influence of the TE's epigenetic regulation on the genome. TE activity is suppressed by small RNAs, which also inhibit viruses and regulate the expression of genes. The production of TE heterochromatin-associated endogenous small interfering RNAs (siRNAs) in the reference plant Arabidopsis thaliana is mechanistically distinct from gene-regulating small RNAs, such as microRNAs or trans-acting siRNAs (tasiRNAs). Previous research identified a TE small RNA that potentially regulates the UBP1b mRNA, which encodes an RNA-binding protein involved in stress granule formation. We demonstrate that this siRNA, siRNA854, is under the same trans-generational epigenetic control as the Athila family LTR retrotransposons from which it is produced. The epigenetic activation of Athila elements results in a shift in small RNA processing pathways, and new 21-22 nucleotide versions of Athila siRNAs are produced by protein components normally not responsible for processing TE siRNAs. This processing results in siRNA854's incorporation into ARGONAUTE1 protein complexes in a similar fashion to gene-regulating tasiRNAs. We have used reporter transgenes to demonstrate that the UPB1b 3' untranslated region directly responds to the epigenetic status of Athila TEs and the accumulation of siRNA854. The regulation of the UPB1b 3' untranslated region occurs both on the post-transcriptional and translational levels when Athila TEs are epigenetically activated, and this regulation results in the phenocopy of the ubp1b mutant stress-sensitive phenotype. This demonstrates that a TE's epigenetic activity can modulate the host organism's stress response. In addition, the ability of this TE siRNA to regulate a gene's expression in trans blurs the lines between TE and gene-regulating small RNAs.
转座元件 (TEs) 的表观遗传活性可以影响基因的调控;然而,这种调控仅限于 TE 附近的基因、启动子和增强子。因此,基因的局部顺式调控限制了 TE 的表观遗传调控对基因组的影响。TE 的活性受到小 RNA 的抑制,小 RNA 还可以抑制病毒并调节基因的表达。在参考植物拟南芥中,TE 异染色质相关内源性小干扰 RNA (siRNA) 的产生在机制上不同于基因调节的小 RNA,如 microRNA 或反式作用 siRNA (tasiRNA)。先前的研究鉴定了一种可能调节 UBP1b mRNA 的 TE 小 RNA,该 mRNA 编码一种参与应激颗粒形成的 RNA 结合蛋白。我们证明,这种 siRNA,即 siRNA854,与它产生的 Athila 家族 LTR 反转录转座子一样,受到跨代表观遗传控制。Athila 元件的表观遗传激活导致小 RNA 加工途径发生转变,并且新的 21-22 个核苷酸版本的 Athila siRNA 由通常不负责处理 TE siRNA 的蛋白质成分产生。这种加工导致 siRNA854 以类似于基因调节 tasiRNA 的方式整合到 ARGONAUTE1 蛋白复合物中。我们使用报告基因转基因来证明 UPB1b 3' 非翻译区直接响应 Athila TE 的表观遗传状态和 siRNA854 的积累。当 Athila TEs 被表观遗传激活时,UPB1b 3' 非翻译区的调节发生在转录后和翻译水平上,这种调节导致 ubp1b 突变体应激敏感表型的表型模拟。这表明 TE 的表观遗传活性可以调节宿主生物体的应激反应。此外,这种 TE siRNA 跨基因调节基因表达的能力模糊了 TE 和基因调节小 RNA 之间的界限。