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Planarians recruit piRNAs for mRNA turnover in adult stem cells

PIWI proteins utilize small RNAs called piRNAs to silence transposable elements, thereby protecting germline integrity. In planarian flatworms, PIWI proteins are essential for regeneration, which requires adult stem cells termed neoblasts. Here, we characterize planarian piRNAs and examine the roles...

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Autores principales: Kim, Iana V., Duncan, Elizabeth M., Ross, Eric J., Gorbovytska, Vladyslava, Nowotarski, Stephanie H., Elliott, Sarah A., Sánchez Alvarado, Alejandro, Kuhn, Claus-D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824462/
https://www.ncbi.nlm.nih.gov/pubmed/31537626
http://dx.doi.org/10.1101/gad.322776.118
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author Kim, Iana V.
Duncan, Elizabeth M.
Ross, Eric J.
Gorbovytska, Vladyslava
Nowotarski, Stephanie H.
Elliott, Sarah A.
Sánchez Alvarado, Alejandro
Kuhn, Claus-D.
author_facet Kim, Iana V.
Duncan, Elizabeth M.
Ross, Eric J.
Gorbovytska, Vladyslava
Nowotarski, Stephanie H.
Elliott, Sarah A.
Sánchez Alvarado, Alejandro
Kuhn, Claus-D.
author_sort Kim, Iana V.
collection PubMed
description PIWI proteins utilize small RNAs called piRNAs to silence transposable elements, thereby protecting germline integrity. In planarian flatworms, PIWI proteins are essential for regeneration, which requires adult stem cells termed neoblasts. Here, we characterize planarian piRNAs and examine the roles of PIWI proteins in neoblast biology. We find that the planarian PIWI proteins SMEDWI-2 and SMEDWI-3 cooperate to degrade active transposons via the ping-pong cycle. Unexpectedly, we discover that SMEDWI-3 plays an additional role in planarian mRNA surveillance. While SMEDWI-3 degrades numerous neoblast mRNAs in a homotypic ping-pong cycle, it is also guided to another subset of neoblast mRNAs by antisense piRNAs and binds these without degrading them. Mechanistically, the distinct activities of SMEDWI-3 are primarily dictated by the degree of complementarity between target mRNAs and antisense piRNAs. Thus, PIWI proteins enable planarians to repurpose piRNAs for potentially critical roles in neoblast mRNA turnover.
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spelling pubmed-68244622020-05-01 Planarians recruit piRNAs for mRNA turnover in adult stem cells Kim, Iana V. Duncan, Elizabeth M. Ross, Eric J. Gorbovytska, Vladyslava Nowotarski, Stephanie H. Elliott, Sarah A. Sánchez Alvarado, Alejandro Kuhn, Claus-D. Genes Dev Research Paper PIWI proteins utilize small RNAs called piRNAs to silence transposable elements, thereby protecting germline integrity. In planarian flatworms, PIWI proteins are essential for regeneration, which requires adult stem cells termed neoblasts. Here, we characterize planarian piRNAs and examine the roles of PIWI proteins in neoblast biology. We find that the planarian PIWI proteins SMEDWI-2 and SMEDWI-3 cooperate to degrade active transposons via the ping-pong cycle. Unexpectedly, we discover that SMEDWI-3 plays an additional role in planarian mRNA surveillance. While SMEDWI-3 degrades numerous neoblast mRNAs in a homotypic ping-pong cycle, it is also guided to another subset of neoblast mRNAs by antisense piRNAs and binds these without degrading them. Mechanistically, the distinct activities of SMEDWI-3 are primarily dictated by the degree of complementarity between target mRNAs and antisense piRNAs. Thus, PIWI proteins enable planarians to repurpose piRNAs for potentially critical roles in neoblast mRNA turnover. Cold Spring Harbor Laboratory Press 2019-11-01 /pmc/articles/PMC6824462/ /pubmed/31537626 http://dx.doi.org/10.1101/gad.322776.118 Text en © 2019 Kim et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six 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/.
spellingShingle Research Paper
Kim, Iana V.
Duncan, Elizabeth M.
Ross, Eric J.
Gorbovytska, Vladyslava
Nowotarski, Stephanie H.
Elliott, Sarah A.
Sánchez Alvarado, Alejandro
Kuhn, Claus-D.
Planarians recruit piRNAs for mRNA turnover in adult stem cells
title Planarians recruit piRNAs for mRNA turnover in adult stem cells
title_full Planarians recruit piRNAs for mRNA turnover in adult stem cells
title_fullStr Planarians recruit piRNAs for mRNA turnover in adult stem cells
title_full_unstemmed Planarians recruit piRNAs for mRNA turnover in adult stem cells
title_short Planarians recruit piRNAs for mRNA turnover in adult stem cells
title_sort planarians recruit pirnas for mrna turnover in adult stem cells
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824462/
https://www.ncbi.nlm.nih.gov/pubmed/31537626
http://dx.doi.org/10.1101/gad.322776.118
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