Maelstrom Represses Canonical Polymerase II Transcription within Bi-directional piRNA Clusters in Drosophila melanogaster
| dc.contributor.author | Chang, Timothy | |
| dc.contributor.author | Mattei, Eugenio | |
| dc.contributor.author | Colpan, Cansu | |
| dc.contributor.author | Weng, Zhiping | |
| dc.contributor.author | Zamore, Phillip D. | |
| dc.date | 2022-08-11T08:07:59.000 | |
| dc.date.accessioned | 2022-08-23T15:38:02Z | |
| dc.date.available | 2022-08-23T15:38:02Z | |
| dc.date.issued | 2018-11-12 | |
| dc.date.submitted | 2019-01-09 | |
| dc.identifier.citation | <p>Mol Cell. 2018 Nov 12. pii: S1097-2765(18)30932-8. doi: 10.1016/j.molcel.2018.10.038. [Epub ahead of print]. <a href="https://doi.org/10.1016/j.molcel.2018.10.038">Link to article on publisher's site</a></p> | |
| dc.identifier.issn | 1097-2765 (Linking) | |
| dc.identifier.doi | 10.1016/j.molcel.2018.10.038 | |
| dc.identifier.pmid | 30527661 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.14038/25850 | |
| dc.description.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. | |
| dc.language.iso | en_US | |
| dc.relation | <p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=30527661&dopt=Abstract">Link to Article in PubMed</a></p> | |
| dc.relation.url | https://doi.org/10.1016/j.molcel.2018.10.038 | |
| dc.subject | Argonaute | |
| dc.subject | Armitage | |
| dc.subject | Maelstrom | |
| dc.subject | PIWI-interacting RNA | |
| dc.subject | Piwi | |
| dc.subject | Rhino | |
| dc.subject | piRNA | |
| dc.subject | small silencing RNA | |
| dc.subject | transcription | |
| dc.subject | transposon | |
| dc.subject | Amino Acids, Peptides, and Proteins | |
| dc.subject | Biochemistry | |
| dc.subject | Bioinformatics | |
| dc.subject | Computational Biology | |
| dc.subject | Genetics and Genomics | |
| dc.subject | Molecular Biology | |
| dc.subject | Nucleic Acids, Nucleotides, and Nucleosides | |
| dc.title | Maelstrom Represses Canonical Polymerase II Transcription within Bi-directional piRNA Clusters in Drosophila melanogaster | |
| dc.type | Journal Article | |
| dc.source.journaltitle | Molecular cell | |
| dc.identifier.legacycoverpage | https://escholarship.umassmed.edu/bioinformatics_pubs/142 | |
| dc.identifier.contextkey | 13591442 | |
| html.description.abstract | <p>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.</p> | |
| dc.identifier.submissionpath | bioinformatics_pubs/142 | |
| dc.contributor.department | Graduate School of Biomedical Sciences | |
| dc.contributor.department | Department of Biochemistry and Molecular Pharmacology | |
| dc.contributor.department | Program in Bioinformatics and Integrative Biology | |
| dc.contributor.department | RNA Therapeutics Institute |