TEX15 is an essential executor of MIWI2-directed transposon DNA methylation and silencing

Theresa Schöpp(MRC Centre for Regenerative Medicine), Ansgar Zoch(MRC Centre for Regenerative Medicine), Rebecca V. Berrens(University of Cambridge), Tania Auchynnikava(Wellcome Centre for Cell Biology), Yuka Kabayama(MRC Centre for Regenerative Medicine), Lina Vasiliauskaitė(MRC Centre for Regenerative Medicine), Juri Rappsilber(Wellcome Centre for Cell Biology), Robin C. Allshire(Wellcome Centre for Cell Biology), Dónal O’Carroll(MRC Centre for Regenerative Medicine)
Nature Communications
July 27, 2020
Cited by 65Open Access
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Abstract

The PIWI protein MIWI2 and its associated PIWI-interacting RNAs (piRNAs) instruct DNA methylation of young active transposable elements (TEs) in the male germline. piRNAs are proposed to recruit MIWI2 to the transcriptionally active TE loci by base pairing to nascent transcripts, however the downstream mechanisms and effector proteins utilized by MIWI2 in directing de novo TE methylation remain incompletely understood. Here, we show that MIWI2 associates with TEX15 in foetal gonocytes. TEX15 is predominantly a nuclear protein that is not required for piRNA biogenesis but is essential for piRNA-directed TE de novo methylation and silencing. In summary, TEX15 is an essential executor of mammalian piRNA-directed DNA methylation.


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