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The PIWI/piRNA response is relaxed in a rodent that lacks mobilizing transposable elements

Transposable elements (TEs) are genomic parasites that can propagate throughout host genomes. Mammalian genomes are typically dominated by LINE retrotransposons and their associated SINEs, and germline mobilization is a challenge to genome integrity. There are defenses against TE proliferation and t...

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Autores principales: Vandewege, Michael W., Patt, Roy N., Merriman, Dana K., Ray, David A., Hoffmann, Federico G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8925971/
https://www.ncbi.nlm.nih.gov/pubmed/35064043
http://dx.doi.org/10.1261/rna.078862.121
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author Vandewege, Michael W.
Patt, Roy N.
Merriman, Dana K.
Ray, David A.
Hoffmann, Federico G.
author_facet Vandewege, Michael W.
Patt, Roy N.
Merriman, Dana K.
Ray, David A.
Hoffmann, Federico G.
author_sort Vandewege, Michael W.
collection PubMed
description Transposable elements (TEs) are genomic parasites that can propagate throughout host genomes. Mammalian genomes are typically dominated by LINE retrotransposons and their associated SINEs, and germline mobilization is a challenge to genome integrity. There are defenses against TE proliferation and the PIWI/piRNA defense is among the most well understood. However, the PIWI/piRNA system has been investigated largely in animals with actively mobilizing TEs and it is unclear how the PIWI/piRNA system functions in the absence of mobilizing TEs. The 13-lined ground squirrel provides the opportunity to examine PIWI/piRNA and TE dynamics within the context of minimal, and possibly nonexistent, TE accumulation. To do so, we compared the PIWI/piRNA dynamics in squirrels to observations from the rabbit and mouse. Despite a lack of young insertions in squirrels, TEs were still actively transcribed at higher levels compared to mouse and rabbit. All three Piwi genes were not expressed, prior to P8 in squirrel testis, and there was little TE expression change with the onset of Piwi expression. We also demonstrated there was not a major expression change in the young squirrel LINE families in the transition from juvenile to adult testis in contrast to young mouse and rabbit LINE families. These observations lead us to conclude that PIWI suppression, was weaker for squirrel LINEs and SINEs and did not strongly reduce their transcription. We speculate that, although the PIWI/piRNA system is adaptable to novel TE threats, transcripts from TEs that are no longer threatening receive less attention from PIWI proteins.
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spelling pubmed-89259712023-04-01 The PIWI/piRNA response is relaxed in a rodent that lacks mobilizing transposable elements Vandewege, Michael W. Patt, Roy N. Merriman, Dana K. Ray, David A. Hoffmann, Federico G. RNA Article Transposable elements (TEs) are genomic parasites that can propagate throughout host genomes. Mammalian genomes are typically dominated by LINE retrotransposons and their associated SINEs, and germline mobilization is a challenge to genome integrity. There are defenses against TE proliferation and the PIWI/piRNA defense is among the most well understood. However, the PIWI/piRNA system has been investigated largely in animals with actively mobilizing TEs and it is unclear how the PIWI/piRNA system functions in the absence of mobilizing TEs. The 13-lined ground squirrel provides the opportunity to examine PIWI/piRNA and TE dynamics within the context of minimal, and possibly nonexistent, TE accumulation. To do so, we compared the PIWI/piRNA dynamics in squirrels to observations from the rabbit and mouse. Despite a lack of young insertions in squirrels, TEs were still actively transcribed at higher levels compared to mouse and rabbit. All three Piwi genes were not expressed, prior to P8 in squirrel testis, and there was little TE expression change with the onset of Piwi expression. We also demonstrated there was not a major expression change in the young squirrel LINE families in the transition from juvenile to adult testis in contrast to young mouse and rabbit LINE families. These observations lead us to conclude that PIWI suppression, was weaker for squirrel LINEs and SINEs and did not strongly reduce their transcription. We speculate that, although the PIWI/piRNA system is adaptable to novel TE threats, transcripts from TEs that are no longer threatening receive less attention from PIWI proteins. Cold Spring Harbor Laboratory Press 2022-04 /pmc/articles/PMC8925971/ /pubmed/35064043 http://dx.doi.org/10.1261/rna.078862.121 Text en © 2022 Vandewege et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society https://creativecommons.org/licenses/by-nc/4.0/This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Article
Vandewege, Michael W.
Patt, Roy N.
Merriman, Dana K.
Ray, David A.
Hoffmann, Federico G.
The PIWI/piRNA response is relaxed in a rodent that lacks mobilizing transposable elements
title The PIWI/piRNA response is relaxed in a rodent that lacks mobilizing transposable elements
title_full The PIWI/piRNA response is relaxed in a rodent that lacks mobilizing transposable elements
title_fullStr The PIWI/piRNA response is relaxed in a rodent that lacks mobilizing transposable elements
title_full_unstemmed The PIWI/piRNA response is relaxed in a rodent that lacks mobilizing transposable elements
title_short The PIWI/piRNA response is relaxed in a rodent that lacks mobilizing transposable elements
title_sort piwi/pirna response is relaxed in a rodent that lacks mobilizing transposable elements
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8925971/
https://www.ncbi.nlm.nih.gov/pubmed/35064043
http://dx.doi.org/10.1261/rna.078862.121
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