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The nascent RNA binding complex SFiNX licenses piRNA-guided heterochromatin formation

The PIWI-interacting RNA (piRNA) pathway protects genome integrity in part through establishing repressive heterochromatin at transposon loci. Silencing requires piRNA-guided targeting of nuclear PIWI proteins to nascent transposon transcripts, yet the subsequent molecular events are not understood....

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Autores principales: Batki, Julia, Schnabl, Jakob, Wang, Juncheng, Handler, Dominik, Andreev, Veselin I., Stieger, Christian E., Novatchkova, Maria, Lampersberger, Lisa, Kauneckaite, Kotryna, Xie, Wei, Mechtler, Karl, Patel, Dinshaw J., Brennecke, Julius
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6828549/
https://www.ncbi.nlm.nih.gov/pubmed/31384064
http://dx.doi.org/10.1038/s41594-019-0270-6
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author Batki, Julia
Schnabl, Jakob
Wang, Juncheng
Handler, Dominik
Andreev, Veselin I.
Stieger, Christian E.
Novatchkova, Maria
Lampersberger, Lisa
Kauneckaite, Kotryna
Xie, Wei
Mechtler, Karl
Patel, Dinshaw J.
Brennecke, Julius
author_facet Batki, Julia
Schnabl, Jakob
Wang, Juncheng
Handler, Dominik
Andreev, Veselin I.
Stieger, Christian E.
Novatchkova, Maria
Lampersberger, Lisa
Kauneckaite, Kotryna
Xie, Wei
Mechtler, Karl
Patel, Dinshaw J.
Brennecke, Julius
author_sort Batki, Julia
collection PubMed
description The PIWI-interacting RNA (piRNA) pathway protects genome integrity in part through establishing repressive heterochromatin at transposon loci. Silencing requires piRNA-guided targeting of nuclear PIWI proteins to nascent transposon transcripts, yet the subsequent molecular events are not understood. Here, we identify SFiNX (Silencing Factor interacting Nuclear eXport variant), an interdependent protein complex required for Piwi-mediated co-transcriptional silencing in Drosophila. SFiNX consists of Nxf2–Nxt1, a gonad-specific variant of the heterodimeric mRNA export receptor Nxf1–Nxt1, and the Piwi-associated protein Panoramix. SFiNX mutant flies are sterile and exhibit transposon de-repression because piRNA-loaded Piwi is unable to establish heterochromatin. Within SFiNX, Panoramix recruits heterochromatin effectors, while the RNA binding protein Nxf2 licenses co-transcriptional silencing. Our data reveal how Nxf2 might have evolved from an RNA transport receptor into a co-transcriptional silencing factor. Thus, NXF variants, which are abundant in metazoans, can have diverse molecular functions and might have been co-opted for host genome defense more broadly.
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spelling pubmed-68285492020-02-05 The nascent RNA binding complex SFiNX licenses piRNA-guided heterochromatin formation Batki, Julia Schnabl, Jakob Wang, Juncheng Handler, Dominik Andreev, Veselin I. Stieger, Christian E. Novatchkova, Maria Lampersberger, Lisa Kauneckaite, Kotryna Xie, Wei Mechtler, Karl Patel, Dinshaw J. Brennecke, Julius Nat Struct Mol Biol Article The PIWI-interacting RNA (piRNA) pathway protects genome integrity in part through establishing repressive heterochromatin at transposon loci. Silencing requires piRNA-guided targeting of nuclear PIWI proteins to nascent transposon transcripts, yet the subsequent molecular events are not understood. Here, we identify SFiNX (Silencing Factor interacting Nuclear eXport variant), an interdependent protein complex required for Piwi-mediated co-transcriptional silencing in Drosophila. SFiNX consists of Nxf2–Nxt1, a gonad-specific variant of the heterodimeric mRNA export receptor Nxf1–Nxt1, and the Piwi-associated protein Panoramix. SFiNX mutant flies are sterile and exhibit transposon de-repression because piRNA-loaded Piwi is unable to establish heterochromatin. Within SFiNX, Panoramix recruits heterochromatin effectors, while the RNA binding protein Nxf2 licenses co-transcriptional silencing. Our data reveal how Nxf2 might have evolved from an RNA transport receptor into a co-transcriptional silencing factor. Thus, NXF variants, which are abundant in metazoans, can have diverse molecular functions and might have been co-opted for host genome defense more broadly. 2019-08-05 2019-08 /pmc/articles/PMC6828549/ /pubmed/31384064 http://dx.doi.org/10.1038/s41594-019-0270-6 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Batki, Julia
Schnabl, Jakob
Wang, Juncheng
Handler, Dominik
Andreev, Veselin I.
Stieger, Christian E.
Novatchkova, Maria
Lampersberger, Lisa
Kauneckaite, Kotryna
Xie, Wei
Mechtler, Karl
Patel, Dinshaw J.
Brennecke, Julius
The nascent RNA binding complex SFiNX licenses piRNA-guided heterochromatin formation
title The nascent RNA binding complex SFiNX licenses piRNA-guided heterochromatin formation
title_full The nascent RNA binding complex SFiNX licenses piRNA-guided heterochromatin formation
title_fullStr The nascent RNA binding complex SFiNX licenses piRNA-guided heterochromatin formation
title_full_unstemmed The nascent RNA binding complex SFiNX licenses piRNA-guided heterochromatin formation
title_short The nascent RNA binding complex SFiNX licenses piRNA-guided heterochromatin formation
title_sort nascent rna binding complex sfinx licenses pirna-guided heterochromatin formation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6828549/
https://www.ncbi.nlm.nih.gov/pubmed/31384064
http://dx.doi.org/10.1038/s41594-019-0270-6
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