| Literature DB >> 31368590 |
Kensaku Murano1, Yuka W Iwasaki1, Hirotsugu Ishizu1, Akane Mashiko1,2, Aoi Shibuya1, Shu Kondo3, Shungo Adachi4, Saori Suzuki5, Kuniaki Saito3, Tohru Natsume4, Mikiko C Siomi5, Haruhiko Siomi1.
Abstract
The PIWI-interacting RNA (piRNA) pathway preserves genomic integrity by repressing transposable elements (TEs) in animal germ cells. Among PIWI-clade proteins in Drosophila, Piwi transcriptionally silences its targets through interactions with cofactors, including Panoramix (Panx) and forms heterochromatin characterized by H3K9me3 and H1. Here, we identified Nxf2, a nuclear RNA export factor (NXF) variant, as a protein that forms complexes with Piwi, Panx, and p15. Panx-Nxf2-P15 complex formation is necessary in the silencing by stabilizing protein levels of Nxf2 and Panx. Notably, ectopic targeting of Nxf2 initiates co-transcriptional repression of the target reporter in a manner independent of H3K9me3 marks or H1. However, continuous silencing requires HP1a and H1. In addition, Nxf2 directly interacts with target TE transcripts in a Piwi-dependent manner. These findings suggest a model in which the Panx-Nxf2-P15 complex enforces the association of Piwi with target transcripts to trigger co-transcriptional repression, prior to heterochromatin formation in the nuclear piRNA pathway. Our results provide an unexpected connection between an NXF variant and small RNA-mediated co-transcriptional silencing.Entities:
Keywords: RNA silencing; heterochromatin formation; nuclear RNA export factor; transcriptional regulation; transposable element
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Year: 2019 PMID: 31368590 PMCID: PMC6717896 DOI: 10.15252/embj.2019102870
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598