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dc.contributor.authorChang, Timothy
dc.contributor.authorMattei, Eugenio
dc.contributor.authorColpan, Cansu
dc.contributor.authorWeng, Zhiping
dc.contributor.authorZamore, Phillip D.
dc.date2022-08-11T08:07:59.000
dc.date.accessioned2022-08-23T15:38:02Z
dc.date.available2022-08-23T15:38:02Z
dc.date.issued2018-11-12
dc.date.submitted2019-01-09
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.issn1097-2765 (Linking)
dc.identifier.doi10.1016/j.molcel.2018.10.038
dc.identifier.pmid30527661
dc.identifier.urihttp://hdl.handle.net/20.500.14038/25850
dc.description.abstractIn 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.isoen_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.urlhttps://doi.org/10.1016/j.molcel.2018.10.038
dc.subjectArgonaute
dc.subjectArmitage
dc.subjectMaelstrom
dc.subjectPIWI-interacting RNA
dc.subjectPiwi
dc.subjectRhino
dc.subjectpiRNA
dc.subjectsmall silencing RNA
dc.subjecttranscription
dc.subjecttransposon
dc.subjectAmino Acids, Peptides, and Proteins
dc.subjectBiochemistry
dc.subjectBioinformatics
dc.subjectComputational Biology
dc.subjectGenetics and Genomics
dc.subjectMolecular Biology
dc.subjectNucleic Acids, Nucleotides, and Nucleosides
dc.titleMaelstrom Represses Canonical Polymerase II Transcription within Bi-directional piRNA Clusters in Drosophila melanogaster
dc.typeJournal Article
dc.source.journaltitleMolecular cell
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/bioinformatics_pubs/142
dc.identifier.contextkey13591442
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.submissionpathbioinformatics_pubs/142
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.contributor.departmentProgram in Bioinformatics and Integrative Biology
dc.contributor.departmentRNA Therapeutics Institute


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