Cargando…
Abundant expression of somatic transposon-derived piRNAs throughout Tribolium castaneum embryogenesis
BACKGROUND: Piwi-interacting RNAs (piRNAs) are a class of short (~26–31-nucleotide) non-protein-coding RNAs expressed in the metazoan germline. The piRNA pathway in arthropods is best understood in the ovary of Drosophila melanogaster, where it acts to silence active transposable elements (TEs). Mat...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613491/ https://www.ncbi.nlm.nih.gov/pubmed/28950880 http://dx.doi.org/10.1186/s13059-017-1304-1 |
_version_ | 1783266268560752640 |
---|---|
author | Ninova, Maria Griffiths-Jones, Sam Ronshaugen, Matthew |
author_facet | Ninova, Maria Griffiths-Jones, Sam Ronshaugen, Matthew |
author_sort | Ninova, Maria |
collection | PubMed |
description | BACKGROUND: Piwi-interacting RNAs (piRNAs) are a class of short (~26–31-nucleotide) non-protein-coding RNAs expressed in the metazoan germline. The piRNA pathway in arthropods is best understood in the ovary of Drosophila melanogaster, where it acts to silence active transposable elements (TEs). Maternal loading of piRNAs in oocytes is further required for the inheritance of piRNA-mediated transposon defence. However, our understanding of the diversity, evolution and function of the piRNA complement beyond drosophilids is limited. The red flour beetle, Tribolium castaneum, is an emerging model organism separated from Drosophila by ~ 350 million years of evolution that displays a number of features ancestral to arthropods, including short germ embryogenesis. Here, we characterize the maternally deposited and zygotically expressed small RNA and mRNA complements throughout T. castaneum embryogenesis. RESULTS: We find that beetle oocytes and embryos of all stages are abundant in heterogeneous ~ 28-nucleotide RNAs. These small RNAs originate from discrete genomic loci enriched in TE sequences and display the molecular signatures of transposon-derived piRNAs. In addition to the maternally loaded primary piRNAs, Tribolium embryos produce secondary piRNAs by the cleavage of zygotically activated TE transcripts via the ping-pong mechanism. The two Tribolium piRNA pathway effector proteins, Tc-Piwi/Aub and Tc-Ago3, are also expressed throughout the soma of early embryos. CONCLUSIONS: Our results show that the piRNA pathway in Tribolium is not restricted to the germline, but also operates in the embryo and may act to antagonize zygotically activated transposons. Taken together, these data highlight a functional divergence of the piRNA pathway between insects. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-017-1304-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5613491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56134912017-10-11 Abundant expression of somatic transposon-derived piRNAs throughout Tribolium castaneum embryogenesis Ninova, Maria Griffiths-Jones, Sam Ronshaugen, Matthew Genome Biol Research BACKGROUND: Piwi-interacting RNAs (piRNAs) are a class of short (~26–31-nucleotide) non-protein-coding RNAs expressed in the metazoan germline. The piRNA pathway in arthropods is best understood in the ovary of Drosophila melanogaster, where it acts to silence active transposable elements (TEs). Maternal loading of piRNAs in oocytes is further required for the inheritance of piRNA-mediated transposon defence. However, our understanding of the diversity, evolution and function of the piRNA complement beyond drosophilids is limited. The red flour beetle, Tribolium castaneum, is an emerging model organism separated from Drosophila by ~ 350 million years of evolution that displays a number of features ancestral to arthropods, including short germ embryogenesis. Here, we characterize the maternally deposited and zygotically expressed small RNA and mRNA complements throughout T. castaneum embryogenesis. RESULTS: We find that beetle oocytes and embryos of all stages are abundant in heterogeneous ~ 28-nucleotide RNAs. These small RNAs originate from discrete genomic loci enriched in TE sequences and display the molecular signatures of transposon-derived piRNAs. In addition to the maternally loaded primary piRNAs, Tribolium embryos produce secondary piRNAs by the cleavage of zygotically activated TE transcripts via the ping-pong mechanism. The two Tribolium piRNA pathway effector proteins, Tc-Piwi/Aub and Tc-Ago3, are also expressed throughout the soma of early embryos. CONCLUSIONS: Our results show that the piRNA pathway in Tribolium is not restricted to the germline, but also operates in the embryo and may act to antagonize zygotically activated transposons. Taken together, these data highlight a functional divergence of the piRNA pathway between insects. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-017-1304-1) contains supplementary material, which is available to authorized users. BioMed Central 2017-09-26 /pmc/articles/PMC5613491/ /pubmed/28950880 http://dx.doi.org/10.1186/s13059-017-1304-1 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Ninova, Maria Griffiths-Jones, Sam Ronshaugen, Matthew Abundant expression of somatic transposon-derived piRNAs throughout Tribolium castaneum embryogenesis |
title | Abundant expression of somatic transposon-derived piRNAs throughout Tribolium castaneum embryogenesis |
title_full | Abundant expression of somatic transposon-derived piRNAs throughout Tribolium castaneum embryogenesis |
title_fullStr | Abundant expression of somatic transposon-derived piRNAs throughout Tribolium castaneum embryogenesis |
title_full_unstemmed | Abundant expression of somatic transposon-derived piRNAs throughout Tribolium castaneum embryogenesis |
title_short | Abundant expression of somatic transposon-derived piRNAs throughout Tribolium castaneum embryogenesis |
title_sort | abundant expression of somatic transposon-derived pirnas throughout tribolium castaneum embryogenesis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613491/ https://www.ncbi.nlm.nih.gov/pubmed/28950880 http://dx.doi.org/10.1186/s13059-017-1304-1 |
work_keys_str_mv | AT ninovamaria abundantexpressionofsomatictransposonderivedpirnasthroughouttriboliumcastaneumembryogenesis AT griffithsjonessam abundantexpressionofsomatictransposonderivedpirnasthroughouttriboliumcastaneumembryogenesis AT ronshaugenmatthew abundantexpressionofsomatictransposonderivedpirnasthroughouttriboliumcastaneumembryogenesis |