| Literature DB >> 30527661 |
Timothy H Chang1, Eugenio Mattei2, Ildar Gainetdinov1, Cansu Colpan1, Zhiping Weng3, Phillip D Zamore4.
Abstract
In Drosophila, 23-30 nt long PIWI-interacting RNAs (piRNAs) direct the protein Piwi to silence germline transposon transcription. Most germline piRNAs derive from dual-strand piRNA clusters, heterochromatic transposon graveyards that are transcribed from both genomic strands. These piRNA sources are marked by the heterochromatin protein 1 homolog Rhino (Rhi), which facilitates their promoter-independent transcription, suppresses splicing, and inhibits transcriptional termination. Here, we report that the protein Maelstrom (Mael) represses canonical, promoter-dependent transcription in dual-strand clusters, allowing Rhi to initiate piRNA precursor transcription. Mael also represses promoter-dependent transcription at sites outside clusters. At some loci, Mael repression requires the piRNA pathway, while at others, piRNAs play no role. We propose that by repressing canonical transcription of individual transposon mRNAs, Mael helps Rhi drive non-canonical transcription of piRNA precursors without generating mRNAs encoding transposon proteins.Entities:
Keywords: Argonaute; Armitage; Maelstrom; PIWI-interacting RNA; Piwi; Rhino; piRNA; small silencing RNA; transcription; transposon
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Year: 2018 PMID: 30527661 PMCID: PMC6551610 DOI: 10.1016/j.molcel.2018.10.038
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970