Cargando…

A piRNA-lncRNA regulatory network initiates responder and trailer piRNA formation during mosquito embryonic development

PIWI-interacting (pi)RNAs are small silencing RNAs that are crucial for the defense against transposable elements in germline tissues of animals. In Aedes aegypti mosquitoes, the piRNA pathway also contributes to gene regulation in somatic tissues, illustrating additional roles for piRNAs and PIWI p...

Descripción completa

Detalles Bibliográficos
Autores principales: Betting, Valerie, Joosten, Joep, Halbach, Rebecca, Thaler, Melissa, Miesen, Pascal, Van Rij, Ronald P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8456997/
https://www.ncbi.nlm.nih.gov/pubmed/34210890
http://dx.doi.org/10.1261/rna.078876.121
_version_ 1784570986462445568
author Betting, Valerie
Joosten, Joep
Halbach, Rebecca
Thaler, Melissa
Miesen, Pascal
Van Rij, Ronald P.
author_facet Betting, Valerie
Joosten, Joep
Halbach, Rebecca
Thaler, Melissa
Miesen, Pascal
Van Rij, Ronald P.
author_sort Betting, Valerie
collection PubMed
description PIWI-interacting (pi)RNAs are small silencing RNAs that are crucial for the defense against transposable elements in germline tissues of animals. In Aedes aegypti mosquitoes, the piRNA pathway also contributes to gene regulation in somatic tissues, illustrating additional roles for piRNAs and PIWI proteins besides transposon repression. Here, we identify a highly abundant endogenous piRNA (propiR1) that associates with both Piwi4 and Piwi5. PropiR1-mediated target silencing requires base-pairing in the seed region with supplemental base-pairing at the piRNA 3′ end. Yet, propiR1 represses a limited set of targets, among which is the lncRNA AAEL027353 (lnc027353). Slicing of lnc027353 initiates production of responder and trailer piRNAs from the cleavage fragment. Expression of propiR1 commences early during embryonic development and mediates degradation of maternally provided lnc027353. Both propiR1 and its lncRNA target are conserved in the closely related Aedes albopictus mosquito, underscoring the importance of this regulatory network for mosquito development.
format Online
Article
Text
id pubmed-8456997
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Cold Spring Harbor Laboratory Press
record_format MEDLINE/PubMed
spelling pubmed-84569972022-10-01 A piRNA-lncRNA regulatory network initiates responder and trailer piRNA formation during mosquito embryonic development Betting, Valerie Joosten, Joep Halbach, Rebecca Thaler, Melissa Miesen, Pascal Van Rij, Ronald P. RNA Article PIWI-interacting (pi)RNAs are small silencing RNAs that are crucial for the defense against transposable elements in germline tissues of animals. In Aedes aegypti mosquitoes, the piRNA pathway also contributes to gene regulation in somatic tissues, illustrating additional roles for piRNAs and PIWI proteins besides transposon repression. Here, we identify a highly abundant endogenous piRNA (propiR1) that associates with both Piwi4 and Piwi5. PropiR1-mediated target silencing requires base-pairing in the seed region with supplemental base-pairing at the piRNA 3′ end. Yet, propiR1 represses a limited set of targets, among which is the lncRNA AAEL027353 (lnc027353). Slicing of lnc027353 initiates production of responder and trailer piRNAs from the cleavage fragment. Expression of propiR1 commences early during embryonic development and mediates degradation of maternally provided lnc027353. Both propiR1 and its lncRNA target are conserved in the closely related Aedes albopictus mosquito, underscoring the importance of this regulatory network for mosquito development. Cold Spring Harbor Laboratory Press 2021-10 /pmc/articles/PMC8456997/ /pubmed/34210890 http://dx.doi.org/10.1261/rna.078876.121 Text en © 2021 Betting 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
Betting, Valerie
Joosten, Joep
Halbach, Rebecca
Thaler, Melissa
Miesen, Pascal
Van Rij, Ronald P.
A piRNA-lncRNA regulatory network initiates responder and trailer piRNA formation during mosquito embryonic development
title A piRNA-lncRNA regulatory network initiates responder and trailer piRNA formation during mosquito embryonic development
title_full A piRNA-lncRNA regulatory network initiates responder and trailer piRNA formation during mosquito embryonic development
title_fullStr A piRNA-lncRNA regulatory network initiates responder and trailer piRNA formation during mosquito embryonic development
title_full_unstemmed A piRNA-lncRNA regulatory network initiates responder and trailer piRNA formation during mosquito embryonic development
title_short A piRNA-lncRNA regulatory network initiates responder and trailer piRNA formation during mosquito embryonic development
title_sort pirna-lncrna regulatory network initiates responder and trailer pirna formation during mosquito embryonic development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8456997/
https://www.ncbi.nlm.nih.gov/pubmed/34210890
http://dx.doi.org/10.1261/rna.078876.121
work_keys_str_mv AT bettingvalerie apirnalncrnaregulatorynetworkinitiatesresponderandtrailerpirnaformationduringmosquitoembryonicdevelopment
AT joostenjoep apirnalncrnaregulatorynetworkinitiatesresponderandtrailerpirnaformationduringmosquitoembryonicdevelopment
AT halbachrebecca apirnalncrnaregulatorynetworkinitiatesresponderandtrailerpirnaformationduringmosquitoembryonicdevelopment
AT thalermelissa apirnalncrnaregulatorynetworkinitiatesresponderandtrailerpirnaformationduringmosquitoembryonicdevelopment
AT miesenpascal apirnalncrnaregulatorynetworkinitiatesresponderandtrailerpirnaformationduringmosquitoembryonicdevelopment
AT vanrijronaldp apirnalncrnaregulatorynetworkinitiatesresponderandtrailerpirnaformationduringmosquitoembryonicdevelopment
AT bettingvalerie pirnalncrnaregulatorynetworkinitiatesresponderandtrailerpirnaformationduringmosquitoembryonicdevelopment
AT joostenjoep pirnalncrnaregulatorynetworkinitiatesresponderandtrailerpirnaformationduringmosquitoembryonicdevelopment
AT halbachrebecca pirnalncrnaregulatorynetworkinitiatesresponderandtrailerpirnaformationduringmosquitoembryonicdevelopment
AT thalermelissa pirnalncrnaregulatorynetworkinitiatesresponderandtrailerpirnaformationduringmosquitoembryonicdevelopment
AT miesenpascal pirnalncrnaregulatorynetworkinitiatesresponderandtrailerpirnaformationduringmosquitoembryonicdevelopment
AT vanrijronaldp pirnalncrnaregulatorynetworkinitiatesresponderandtrailerpirnaformationduringmosquitoembryonicdevelopment