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Channel nuclear pore complex subunits are required for transposon silencing in Drosophila

The nuclear pore complex (NPC) is the principal gateway between nucleus and cytoplasm that enables exchange of macromolecular cargo. Composed of multiple copies of ~30 different nucleoporins (Nups), the NPC acts as a selective portal, interacting with factors which individually license passage of sp...

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Autores principales: Munafò, Marzia, Lawless, Victoria R, Passera, Alessandro, MacMillan, Serena, Bornelöv, Susanne, Haussmann, Irmgard U, Soller, Matthias, Hannon, Gregory J, Czech, Benjamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8133776/
https://www.ncbi.nlm.nih.gov/pubmed/33856346
http://dx.doi.org/10.7554/eLife.66321
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author Munafò, Marzia
Lawless, Victoria R
Passera, Alessandro
MacMillan, Serena
Bornelöv, Susanne
Haussmann, Irmgard U
Soller, Matthias
Hannon, Gregory J
Czech, Benjamin
author_facet Munafò, Marzia
Lawless, Victoria R
Passera, Alessandro
MacMillan, Serena
Bornelöv, Susanne
Haussmann, Irmgard U
Soller, Matthias
Hannon, Gregory J
Czech, Benjamin
author_sort Munafò, Marzia
collection PubMed
description The nuclear pore complex (NPC) is the principal gateway between nucleus and cytoplasm that enables exchange of macromolecular cargo. Composed of multiple copies of ~30 different nucleoporins (Nups), the NPC acts as a selective portal, interacting with factors which individually license passage of specific cargo classes. Here we show that two Nups of the inner channel, Nup54 and Nup58, are essential for transposon silencing via the PIWI-interacting RNA (piRNA) pathway in the Drosophila ovary. In ovarian follicle cells, loss of Nup54 and Nup58 results in compromised piRNA biogenesis exclusively from the flamenco locus, whereas knockdowns of other NPC subunits have widespread consequences. This provides evidence that some Nups can acquire specialised roles in tissue-specific contexts. Our findings consolidate the idea that the NPC has functions beyond simply constituting a barrier to nuclear/cytoplasmic exchange as genomic loci subjected to strong selective pressure can exploit NPC subunits to facilitate their expression.
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spelling pubmed-81337762021-05-21 Channel nuclear pore complex subunits are required for transposon silencing in Drosophila Munafò, Marzia Lawless, Victoria R Passera, Alessandro MacMillan, Serena Bornelöv, Susanne Haussmann, Irmgard U Soller, Matthias Hannon, Gregory J Czech, Benjamin eLife Cell Biology The nuclear pore complex (NPC) is the principal gateway between nucleus and cytoplasm that enables exchange of macromolecular cargo. Composed of multiple copies of ~30 different nucleoporins (Nups), the NPC acts as a selective portal, interacting with factors which individually license passage of specific cargo classes. Here we show that two Nups of the inner channel, Nup54 and Nup58, are essential for transposon silencing via the PIWI-interacting RNA (piRNA) pathway in the Drosophila ovary. In ovarian follicle cells, loss of Nup54 and Nup58 results in compromised piRNA biogenesis exclusively from the flamenco locus, whereas knockdowns of other NPC subunits have widespread consequences. This provides evidence that some Nups can acquire specialised roles in tissue-specific contexts. Our findings consolidate the idea that the NPC has functions beyond simply constituting a barrier to nuclear/cytoplasmic exchange as genomic loci subjected to strong selective pressure can exploit NPC subunits to facilitate their expression. eLife Sciences Publications, Ltd 2021-04-15 /pmc/articles/PMC8133776/ /pubmed/33856346 http://dx.doi.org/10.7554/eLife.66321 Text en © 2021, Munafò et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Munafò, Marzia
Lawless, Victoria R
Passera, Alessandro
MacMillan, Serena
Bornelöv, Susanne
Haussmann, Irmgard U
Soller, Matthias
Hannon, Gregory J
Czech, Benjamin
Channel nuclear pore complex subunits are required for transposon silencing in Drosophila
title Channel nuclear pore complex subunits are required for transposon silencing in Drosophila
title_full Channel nuclear pore complex subunits are required for transposon silencing in Drosophila
title_fullStr Channel nuclear pore complex subunits are required for transposon silencing in Drosophila
title_full_unstemmed Channel nuclear pore complex subunits are required for transposon silencing in Drosophila
title_short Channel nuclear pore complex subunits are required for transposon silencing in Drosophila
title_sort channel nuclear pore complex subunits are required for transposon silencing in drosophila
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8133776/
https://www.ncbi.nlm.nih.gov/pubmed/33856346
http://dx.doi.org/10.7554/eLife.66321
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