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dc.contributor.authorZhang, Gen
dc.contributor.authorYu, Tianxiong
dc.contributor.authorParhad, Swapnil
dc.contributor.authorHo, Samantha
dc.contributor.authorWeng, Zhiping
dc.contributor.authorTheurkauf, William E.
dc.date2022-08-11T08:08:28.000
dc.date.accessioned2022-08-23T15:56:12Z
dc.date.available2022-08-23T15:56:12Z
dc.date.issued2021-09-27
dc.date.submitted2021-12-20
dc.identifier.citation<p>Zhang G, Yu T, Parhad SS, Ho S, Weng Z, Theurkauf WE. piRNA-independent transposon silencing by the Drosophila THO complex. Dev Cell. 2021 Sep 27;56(18):2623-2635.e5. doi: 10.1016/j.devcel.2021.08.021. Epub 2021 Sep 20. PMID: 34547226; PMCID: PMC8567991. <a href="https://doi.org/10.1016/j.devcel.2021.08.021">Link to article on publisher's site</a></p>
dc.identifier.issn1534-5807 (Linking)
dc.identifier.doi10.1016/j.devcel.2021.08.021
dc.identifier.pmid34547226
dc.identifier.urihttp://hdl.handle.net/20.500.14038/29918
dc.description.abstractpiRNAs guide Piwi/Panoramix-dependent H3K9me3 chromatin modification and transposon silencing during Drosophila germline development. The THO RNA export complex is composed of Hpr1, Tho2, and Thoc5-7. Null thoc7 mutations, which displace Thoc5 and Thoc6 from a Tho2-Hpr1 subcomplex, reduce expression of a subset of germline piRNAs and increase transposon expression, suggesting that THO silences transposons by promoting piRNA biogenesis. Here, we show that the thoc7-null mutant combination increases transposon transcription but does not reduce anti-sense piRNAs targeting half of the transcriptionally activated transposon families. These mutations also fail to reduce piRNA-guided H3K9me3 chromatin modification or block Panoramix-dependent silencing of a reporter transgene, and unspliced transposon transcripts co-precipitate with THO through a Piwi- and Panoramix-independent mechanism. Mutations in piwi also dominantly enhance germline defects associated with thoc7-null alleles. THO thus functions in a piRNA-independent transposon-silencing pathway, which acts cooperatively with Piwi to support germline development.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=34547226&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1016/j.devcel.2021.08.021
dc.subjectH3K4me2
dc.subjectH3K9me3
dc.subjectPiwi
dc.subjectTHO
dc.subjectThoc7
dc.subjectgermline development
dc.subjectpiRNA
dc.subjecttranscriptional silencing
dc.subjecttransposon silencing
dc.subjectAmino Acids, Peptides, and Proteins
dc.subjectCell and Developmental Biology
dc.subjectNucleic Acids, Nucleotides, and Nucleosides
dc.titlepiRNA-independent transposon silencing by the Drosophila THO complex
dc.typeJournal Article
dc.source.journaltitleDevelopmental cell
dc.source.volume56
dc.source.issue18
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/faculty_pubs/2121
dc.identifier.contextkey26908860
html.description.abstract<p>piRNAs guide Piwi/Panoramix-dependent H3K9me3 chromatin modification and transposon silencing during Drosophila germline development. The THO RNA export complex is composed of Hpr1, Tho2, and Thoc5-7. Null thoc7 mutations, which displace Thoc5 and Thoc6 from a Tho2-Hpr1 subcomplex, reduce expression of a subset of germline piRNAs and increase transposon expression, suggesting that THO silences transposons by promoting piRNA biogenesis. Here, we show that the thoc7-null mutant combination increases transposon transcription but does not reduce anti-sense piRNAs targeting half of the transcriptionally activated transposon families. These mutations also fail to reduce piRNA-guided H3K9me3 chromatin modification or block Panoramix-dependent silencing of a reporter transgene, and unspliced transposon transcripts co-precipitate with THO through a Piwi- and Panoramix-independent mechanism. Mutations in piwi also dominantly enhance germline defects associated with thoc7-null alleles. THO thus functions in a piRNA-independent transposon-silencing pathway, which acts cooperatively with Piwi to support germline development.</p>
dc.identifier.submissionpathfaculty_pubs/2121
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.contributor.departmentProgram in Bioinformatics and Integrative Biology
dc.contributor.departmentProgram in Molecular Medicine
dc.source.pages2623-2635.e5


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