Maelstrom Represses Canonical Polymerase II Transcription within Bi-directional piRNA Clusters in Drosophila melanogaster
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UMass Chan Affiliations
Graduate School of Biomedical SciencesDepartment of Biochemistry and Molecular Pharmacology
Program in Bioinformatics and Integrative Biology
RNA Therapeutics Institute
Document Type
Journal ArticlePublication Date
2018-11-12Keywords
ArgonauteArmitage
Maelstrom
PIWI-interacting RNA
Piwi
Rhino
piRNA
small silencing RNA
transcription
transposon
Amino Acids, Peptides, and Proteins
Biochemistry
Bioinformatics
Computational Biology
Genetics and Genomics
Molecular Biology
Nucleic Acids, Nucleotides, and Nucleosides
Metadata
Show full item recordAbstract
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.Source
Mol Cell. 2018 Nov 12. pii: S1097-2765(18)30932-8. doi: 10.1016/j.molcel.2018.10.038. [Epub ahead of print]. Link to article on publisher's site
DOI
10.1016/j.molcel.2018.10.038Permanent Link to this Item
http://hdl.handle.net/20.500.14038/25850PubMed ID
30527661Related Resources
ae974a485f413a2113503eed53cd6c53
10.1016/j.molcel.2018.10.038