Abstract

Transposable elements (TE) usually take up a substantial portion of eukaryotic genome. Activities of TEs can cause genome instability or gene mutations that are harmful or even disastrous to the host. TEs also contribute to gene and genome evolution at many aspects. Part of miRNA genes in mammals have been found to derive from transposons while convincing evidences are absent for plants. We found that a considerable number of previously annotated plant miRNAs are identical or homologous to transposons (TE-MIR), which include a small number of bona fide miRNA genes that conform to generally accepted plant miRNA annotation rules, and hairpin derived siRNAs likely to be pre-evolved miRNAs. Analysis of these TE-MIRs indicate that transitions from the medium to high copy TEs into miRNA genes may undergo steps such as inverted repeat formation, sequence speciation and adaptation to miRNA biogenesis. We also identified initial target genes of the TE-MIRs, which contain homologous sequences in their CDS as consequence of cognate TE insertions. About one-third of the initial target mRNAs are supported by publicly available degradome sequencing data for TE-MIR sRNA induced cleavages. Targets of the TE-MIRs are biased to non-TE related genes indicating their penchant to acquire cellular functions during evolution. Interestingly, most of these TE insertions span boundaries between coding and non-coding sequences indicating their incorporation into CDS through alteration of splicing or translation start or stop signals. Taken together, our findings suggest that TEs in gene rich regions can form foldbacks in non-coding part of transcripts that may eventually evolve into miRNA genes or be integrated into protein coding sequences to form potential targets in a “temperate” manner. Thus, transposons may supply as resources for the evolution of miRNA-target interactions in plants.

Highlights

  • Transposable elements (TEs) are able to mobilize and propagate in the host genomes

  • Accumulating evidences from studies in animals support the genesis of a substantial portion of miRNA genes from TEs and other genomic repeats [17,19,20,21]

  • From a considerable amount of TE related MIRs (TE-MIR), we identified a small number of bona fide miRNAs that suffice the current plant miRNA annotation rules [14]

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Summary

Introduction

Transposable elements (TEs) are able to mobilize and propagate in the host genomes. Small RNA dependent silencing mechanisms have evolved to harness the activity of the TEs in eukaryotes [3,4,5]. The ,24-nt rasiRNAs are processed from TE-derived transcripts by dicer-like enzymes and loaded into RISC (RNA Induced Silencing Complex), in which Argonaute proteins play key roles, to guide DNA methylation and/or repressive histone modification. Piwi Interacting RNAs (piRNA) play a role in TE silencing in the germline Piwi proteins, another clade of Argonaute proteins, bind piRNAs to induce silencing of TEs via cleavage of transcripts, DNA methylation or histone modification [3,5]. The TE silencing relies on the major RNAi components, such as Argonaute proteins, Dicer or Dicer-like enzymes and RNA dependent RNA polymerase (RDRP)

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