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全基因组鉴定转座元件小干扰 RNA 反式调控的基因。

Genome-wide identification of genes regulated in trans by transposable element small interfering RNAs.

机构信息

Department of Molecular Genetics & Center for RNA Biology; The Ohio State University; Columbus, OH, USA.

出版信息

RNA Biol. 2013 Aug;10(8):1379-95. doi: 10.4161/rna.25555. Epub 2013 Jul 2.

Abstract

Transposable elements (TEs) are known to influence the regulation of neighboring genes through a variety of mechanisms. Additionally, it was recently discovered that TEs can regulate non-neighboring genes through the trans-acting nature of small interfering RNAs (siRNAs). When the epigenetic repression of TEs is lost, TEs become transcriptionally active, and the host cell acts to repress mutagenic transposition by degrading TE mRNAs into siRNAs. In this study, we have performed a genome-wide analysis in the model plant Arabidopsis thaliana and found that TE siRNA-based regulation of genic mRNAs is more pervasive than the two formerly characterized proof-of-principle examples. We identified 27 candidate genic mRNAs that do not contain a TE fragment but are regulated through partial complementarity by the accumulation of TE siRNAs and are therefore influenced by TE epigenetic activation. We have experimentally confirmed several gene targets and demonstrated that they respond to the accumulation of specific 21 nucleotide TE siRNAs that are incorporated into the Arabidopsis Argonaute1 protein. Additionally, we found that one TE siRNA specifically targets and inhibits the formation of a host protein that acts to repress TE activity, suggesting that TEs harbor and potentially evolutionarily select short sequences to act as suppressors of host TE repression.

摘要

转座元件 (TEs) 已知通过多种机制影响邻近基因的调控。此外,最近发现 TEs 可以通过小干扰 RNA (siRNA) 的反式作用来调节非邻近基因。当 TEs 的表观遗传抑制丢失时,TEs 变得转录活跃,宿主细胞通过将 TE mRNA 降解为 siRNA 来抑制致突变转座。在这项研究中,我们在模式植物拟南芥中进行了全基因组分析,发现基于 TE siRNA 的基因 mRNA 调控比以前描述的两个原理验证例子更为普遍。我们鉴定了 27 个候选基因 mRNA,它们不包含 TE 片段,但通过 TE siRNA 的积累部分互补性进行调控,因此受 TE 表观遗传激活的影响。我们通过实验验证了几个基因靶标,并证明它们对特定 21 个核苷酸的 TE siRNA 的积累有反应,这些 siRNA 被整合到拟南芥 Argonaute1 蛋白中。此外,我们发现一个 TE siRNA 特异性靶向并抑制形成一种宿主蛋白的形成,该蛋白可抑制 TE 活性,表明 TEs 拥有并可能进化选择短序列作为宿主 TE 抑制的抑制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fae6/3817159/7fd2b9251eca/rna-10-1379-g1A_D.jpg

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