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BMC Evol Biol. 2018 Nov 1;18(1):160. doi: 10.1186/s12862-018-1274-2.

Diverse RNA interference strategies in early-branching metazoans.

Author information

1
School of Biological Sciences, University of Queensland, Brisbane, QLD, 4072, Australia.
2
Present address: Department of Integrative Zoology, University of Vienna, Althanstraße 1, 4A-1090, Vienna, Austria.
3
Present address: CONACYT, Laboratorio Nacional de Genómica para la Biodiversidad (Langebio). CINVESTAV, Irapuato, Guanajuato, Mexico.
4
Institute for Molecular Bioscience, University of Queensland, Brisbane, QLD, 4072, Australia.
5
Illumina Inc, San Diego, California, 92122, USA.
6
School of Biological Sciences, University of Queensland, Brisbane, QLD, 4072, Australia. b.degnan@uq.edu.au.

Abstract

BACKGROUND:

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.

RESULTS:

Here 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.

CONCLUSION:

Together, 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.

KEYWORDS:

Cnidarian; Ctenophore; Demosponge; Endo-siRNA; Non-bilaterian; RNAi; miRNA; piRNA

PMID:
30382896
PMCID:
PMC6211395
DOI:
10.1186/s12862-018-1274-2
[Indexed for MEDLINE]
Free PMC Article

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