TY - JOUR
T1 - Nuclear RNA export factor variant initiates piRNA-guided co-transcriptional silencing
AU - Murano, Kensaku
AU - Iwasaki, Yuka W.
AU - Ishizu, Hirotsugu
AU - Mashiko, Akane
AU - Shibuya, Aoi
AU - Kondo, Shu
AU - Adachi, Shungo
AU - Suzuki, Saori
AU - Saito, Kuniaki
AU - Natsume, Tohru
AU - Siomi, Mikiko C.
AU - Siomi, Haruhiko
N1 - Funding Information:
We thank Wataru Ito for experimental support and critical discussions. We also thank Julius Brennecke for sharing plasmids; Kazumichi Nishida, Ryo Ohnishi, and Tatsuki Kinoshita for sharing protocols; and Soichiro Yamanaka for critical reading of the paper. This work was supported by funding from JSPS KAKENHI Grant Number 17K08644 and Kato Memorial Bioscience Foundation to K.M.; from JSPS KAKENHI Grant Numbers 15H05583, 17H05603, 18H02421, and 19H05268, Senri Life Science Foundation, NOVARTIS Foundation (Japan), and the Naito Foundation to Y.W.I.; from JSPS KAKENHI Grant Number 17H05610 to S.A.; from Takeda Science Foundation to T.N.; and from JSPS KAKENHI Grant Number 25221003 to H.S.
Publisher Copyright:
© 2019 The Authors
PY - 2019/9/2
Y1 - 2019/9/2
N2 - 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.
AB - 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.
KW - RNA silencing
KW - heterochromatin formation
KW - nuclear RNA export factor
KW - transcriptional regulation
KW - transposable element
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U2 - 10.15252/embj.2019102870
DO - 10.15252/embj.2019102870
M3 - Article
C2 - 31368590
AN - SCOPUS:85070104365
SN - 0261-4189
VL - 38
JO - EMBO Journal
JF - EMBO Journal
IS - 17
M1 - e102870
ER -