Abstract
BackgroundMicro RNAs (miRNAs) and piwi interacting RNAs (piRNAs), along with the more ancient eukaryotic endogenous small interfering RNAs (endo-siRNAs) constitute the principal components of the RNA interference (RNAi) repertoire of most animals. RNAi in non-bilaterians – sponges, ctenophores, placozoans and cnidarians - appears to be more diverse than that of bilaterians, and includes structurally variable miRNAs in sponges, an enormous number of piRNAs in cnidarians and the absence of miRNAs in ctenophores and placozoans.ResultsHere we identify thousands of endo-siRNAs and piRNAs from the sponge Amphimedon queenslandica, the ctenophore Mnemiopsis leidyi and the cnidarian Nematostella vectensis using a computational approach that clusters mapped small RNA sequences and annotates each cluster based on the read length and relative abundance of the constituent reads. This approach was validated on 11 small RNA libraries in Drosophila melanogaster, demonstrating the successful annotation of RNAi-associated loci with properties consistent with previous reports. In the non-bilaterians we uncover seven new miRNAs from Amphimedon and four from Nematostella as well as sub-populations of candidate cis-natural antisense transcript (cis-NAT) endo-siRNAs. We confirmed the absence of miRNAs in Mnemiopsis but detected an abundance of endo-siRNAs in this ctenophore. Analysis of putative piRNA structure suggests that conserved localised secondary structures in primary transcripts may be important for the production of mature piRNAs in Amphimedon and Nematostella, as is also the case for endo-siRNAs.ConclusionTogether, these findings suggest that the last common ancestor of extant animals did not have the entrained RNAi system that typifies bilaterians. Instead it appears that bilaterians, cnidarians, ctenophores and sponges express unique repertoires and combinations of miRNAs, piRNAs and endo-siRNAs.
Highlights
Micro RNAs and piwi interacting RNAs, along with the more ancient eukaryotic endogenous small interfering RNAs constitute the principal components of the RNA interference (RNAi) repertoire of most animals
The uniformity index as a tool for discriminating RNAi classes To investigate the sRNA repertoires of Amphimedon, Mnemiopsis and Nematostella, we developed a method for the annotation of putative precursor transcripts of endosiRNAs, Piwi-interacting RNA (piRNA) and Micro RNA (miRNA) based on Illumina sequenced small RNA libraries
PiRNA biogenesis involves limited specificity over the 5′ and 3′ ends produced by the catalytic components of the pathway, resulting in a highly diverse population of piRNAs generally 26–30 nt in length arising from each loci [43,44,45,46,47]
Summary
Micro RNAs (miRNAs) and piwi interacting RNAs (piRNAs), along with the more ancient eukaryotic endogenous small interfering RNAs (endo-siRNAs) constitute the principal components of the RNA interference (RNAi) repertoire of most animals. RNAi in non-bilaterians – sponges, ctenophores, placozoans and cnidarians - appears to be more diverse than that of bilaterians, and includes structurally variable miRNAs in sponges, an enormous number of piRNAs in cnidarians and the absence of miRNAs in ctenophores and placozoans. Three independent RNAi systems comprise the bulk of the small RNA (sRNA) repertoire: micro RNAs (miRNAs); Piwi interacting RNAs (piRNAs); and endogenous small interfering RNAs (endo-siRNAs). Amongst nonbilaterian animals - sponges, cnidarians ctenophores and placozoans - miRNAs appear to be lost in placozoans and ctenophores with these lineages lacking key miRNA biogenic enzymes [2,3,4]. In Amphimedon, these differ from other metazoan miRNAs in having a peculiar plant-like pre-miRNA secondary structure, and have no discernible homology with any animal miRNAs, except those found in in other demosponges [2, 24,25,26,27]
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