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Levels of P-element-induced hybrid dysgenesis in Drosophila simulans are uncorrelated with levels of P-element piRNAs

Transposable elements (TEs) are genomic parasites that proliferate within host genomes, and which can also invade new species. The P-element, a DNA-based TE, recently invaded two Drosophila species: Drosophila melanogaster in the 20th century, and D. simulans in the 21st. In both species, lines coll...

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Autores principales: Paulouskaya, Olga, Romero-Soriano, Valèria, Ramirez-Lanzas, Claudia, Price, Tom A R, Betancourt, Andrea J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9911080/
https://www.ncbi.nlm.nih.gov/pubmed/36478025
http://dx.doi.org/10.1093/g3journal/jkac324
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author Paulouskaya, Olga
Romero-Soriano, Valèria
Ramirez-Lanzas, Claudia
Price, Tom A R
Betancourt, Andrea J
author_facet Paulouskaya, Olga
Romero-Soriano, Valèria
Ramirez-Lanzas, Claudia
Price, Tom A R
Betancourt, Andrea J
author_sort Paulouskaya, Olga
collection PubMed
description Transposable elements (TEs) are genomic parasites that proliferate within host genomes, and which can also invade new species. The P-element, a DNA-based TE, recently invaded two Drosophila species: Drosophila melanogaster in the 20th century, and D. simulans in the 21st. In both species, lines collected before the invasion are susceptible to “hybrid dysgenesis”, a syndrome of abnormal phenotypes apparently due to P-element-inflicted DNA damage. In D. melanogaster, lines collected after the invasion have evolved a maternally acting mechanism that suppresses hybrid dysgenesis, with extensive work showing that PIWI-interacting small RNAs (piRNAs) are a key factor in this suppression. Most of these studies use lines collected many generations after the initial P-element invasion. Here, we study D. simulans collected early, as well as late in the P-element invasion of this species. Like D. melanogaster, D. simulans from late in the invasion show strong resistance to hybrid dysgenesis and abundant P-element-derived piRNAs. Lines collected early in the invasion, however, show substantial variation in how much they suffer from hybrid dysgenesis, with some lines highly resistant. Surprisingly, although, these resistant lines do not show high levels of cognate maternal P-element piRNAs; in these lines, it may be that other mechanisms suppress hybrid dysgenesis.
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spelling pubmed-99110802023-02-13 Levels of P-element-induced hybrid dysgenesis in Drosophila simulans are uncorrelated with levels of P-element piRNAs Paulouskaya, Olga Romero-Soriano, Valèria Ramirez-Lanzas, Claudia Price, Tom A R Betancourt, Andrea J G3 (Bethesda) Investigation Transposable elements (TEs) are genomic parasites that proliferate within host genomes, and which can also invade new species. The P-element, a DNA-based TE, recently invaded two Drosophila species: Drosophila melanogaster in the 20th century, and D. simulans in the 21st. In both species, lines collected before the invasion are susceptible to “hybrid dysgenesis”, a syndrome of abnormal phenotypes apparently due to P-element-inflicted DNA damage. In D. melanogaster, lines collected after the invasion have evolved a maternally acting mechanism that suppresses hybrid dysgenesis, with extensive work showing that PIWI-interacting small RNAs (piRNAs) are a key factor in this suppression. Most of these studies use lines collected many generations after the initial P-element invasion. Here, we study D. simulans collected early, as well as late in the P-element invasion of this species. Like D. melanogaster, D. simulans from late in the invasion show strong resistance to hybrid dysgenesis and abundant P-element-derived piRNAs. Lines collected early in the invasion, however, show substantial variation in how much they suffer from hybrid dysgenesis, with some lines highly resistant. Surprisingly, although, these resistant lines do not show high levels of cognate maternal P-element piRNAs; in these lines, it may be that other mechanisms suppress hybrid dysgenesis. Oxford University Press 2022-12-08 /pmc/articles/PMC9911080/ /pubmed/36478025 http://dx.doi.org/10.1093/g3journal/jkac324 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Genetics Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigation
Paulouskaya, Olga
Romero-Soriano, Valèria
Ramirez-Lanzas, Claudia
Price, Tom A R
Betancourt, Andrea J
Levels of P-element-induced hybrid dysgenesis in Drosophila simulans are uncorrelated with levels of P-element piRNAs
title Levels of P-element-induced hybrid dysgenesis in Drosophila simulans are uncorrelated with levels of P-element piRNAs
title_full Levels of P-element-induced hybrid dysgenesis in Drosophila simulans are uncorrelated with levels of P-element piRNAs
title_fullStr Levels of P-element-induced hybrid dysgenesis in Drosophila simulans are uncorrelated with levels of P-element piRNAs
title_full_unstemmed Levels of P-element-induced hybrid dysgenesis in Drosophila simulans are uncorrelated with levels of P-element piRNAs
title_short Levels of P-element-induced hybrid dysgenesis in Drosophila simulans are uncorrelated with levels of P-element piRNAs
title_sort levels of p-element-induced hybrid dysgenesis in drosophila simulans are uncorrelated with levels of p-element pirnas
topic Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9911080/
https://www.ncbi.nlm.nih.gov/pubmed/36478025
http://dx.doi.org/10.1093/g3journal/jkac324
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