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A heterochromatin-dependent transcription machinery drives piRNA expression
Open accessAbstract
Nuclear small RNA pathways safeguard genome integrity by establishing transcription-repressing heterochromatin at transposable elements. This inevitably also targets the transposon-rich source loci of the small RNAs themselves. How small RNA source loci are efficiently transcribed while transposon promoters are potently silenced is not understood. Here we show that, in Drosophila, transcription of PIWI-interacting RNA (piRNA) clusters-small RNA source loci in animal gonads-is enforced through RNA polymerase II pre-initiation complex formation within repressive heterochromatin. This is accomplished through Moonshiner, a paralogue of a basal transcription factor IIA (TFIIA) subunit, which is recruited to piRNA clusters via the heterochromatin protein-1 variant Rhino. Moonshiner triggers transcription initiation within piRNA clusters by recruiting the TATA-box binding protein (TBP)-related factor TRF2, an animal TFIID core variant. Thus, transcription of heterochromatic small RNA source loci relies on direct recruitment of the core transcriptional machinery to DNA via histone marks rather than sequence motifs, a concept that we argue is a recurring theme in evolution.
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“Based on current understanding, cells have two layers of defense against potentially deleterious transposable element activation: 1) Transposable element transcription is limited by heterochromatin-mediated silencing, and 2) Transposable element transcripts are cleared from the cell by piRNA-mediated degradation”
From Pathogenic tau-induced piRNA depletion promotes neuronal death through transposable element dysregulation in neurodegenerative tauopathies (2018) · cites this paper as [39]
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Cites
Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
Altschul, S. (1997) · Nucleic Acids Research · doi:10.1093/nar/25.17.3389 · Cited by 73,302
Fiji: an open-source platform for biological-image analysis
Schindelin, J., Arganda-Carreras, I., Frise, E., Kaynig, V., Longair, M., Pietzsch, T., Preibisch, S., Rueden, C., Saalfeld, S., Schmid, B., et al. (2012) · Nature Methods · doi:10.1038/nmeth.2019 · Cited by 66,890
STAR: ultrafast universal RNA-seq aligner
Dobin, A., Davis, C. A., Schlesinger, F., Drenkow, J., Zaleski, C., Jha, S., Batut, P., Chaisson, M., & Gingeras, T. R. (2013) · Bioinformatics · doi:10.1093/bioinformatics/bts635 · Cited by 51,709
limma powers differential expression analyses for RNA-sequencing and microarray studies
Ritchie, M. E., Phipson, B., Wu, D., Hu, Y., Law, C. W., Shi, W., & Smyth, G. K. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv007 · Cited by 40,458
Wickham, H. (2016) · Use R! · doi:10.1007/978-3-319-24277-4 · Cited by 34,873
A Programmable Dual-RNA–Guided DNA Endonuclease in Adaptive Bacterial Immunity
Jinek, M., Chylinski, K., Fonfara, I., Hauer, M., Doudna, J. A., & Charpentier, E. (2012) · Science · doi:10.1126/science.1225829 · Cited by 17,116
Salmon provides fast and bias-aware quantification of transcript expression
Patro, R., Duggal, G., Love, M. I., Irizarry, R. A., & Kingsford, C. (2017) · Nature Methods · doi:10.1038/nmeth.4197 · Cited by 12,700
The Human Genome Browser at UCSC
Kent, W. J., Sugnet, C. W., Furey, T. S., Roskin, K. M., Pringle, T. H., Zahler, A. M., & Haussler, A. D. (2002) · Genome Research · doi:10.1101/gr.229102 · Cited by 10,400
Jalview Version 2—a multiple sequence alignment editor and analysis workbench
Waterhouse, A. M., Procter, J. B., Martin, D. M. A., Clamp, M. E., & Barton, G. J. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp033 · Cited by 10,349
Accelerated Profile HMM Searches
Eddy, S. R. (2011) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002195 · Cited by 6,975
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Haberle, V., & Stark, A. (2018) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-018-0028-8 · Cited by 774
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Cramer, P. (2019) · Nature · doi:10.1038/s41586-019-1517-4 · Cited by 793
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Czech, B., Munafò, M., Ciabrelli, F., Eastwood, E. L., Fabry, M., Kneuss, E., & Hannon, G. J. (2018) · Annual Review of Genetics · doi:10.1146/annurev-genet-120417-031441 · Cited by 569
Sun, W., Samimi, H., Gamez, M., Zare, H., & Frost, B. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0194-1 · Cited by 300
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Wang, X., Ramat, A., Simonelig, M., & Liu, M. (2022) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-022-00528-0 · Cited by 300
Gainetdinov, I. V., Colpan, C., Arif, A., Cecchini, K. R., & Zamore, P. D. (2018) · Molecular Cell · doi:10.1016/j.molcel.2018.08.007 · Cited by 225
Wierzbicki, A. T., Blevins, T., & Świeżewski, S. (2021) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-093020-035446 · Cited by 191
piRNA Biogenesis in Drosophila melanogaster
Huang, X., Tóth, K. F., & Aravin, A. A. (2017) · Trends in Genetics · doi:10.1016/j.tig.2017.09.002 · Cited by 185
The control of gene expression and cell identity by H3K9 trimethylation
Ninova, M., Tóth, K. F., & Aravin, A. A. (2019) · Development · doi:10.1242/dev.181180 · Cited by 170
Locus-specific control of the de novo DNA methylation pathway in Arabidopsis by the CLASSY family
Zhou, M., Palanca, A. M. S., & Law, J. A. (2018) · Nature Genetics · doi:10.1038/s41588-018-0115-y · Cited by 157
Tassetto, M., Kunitomi, M., Whitfield, Z. J., Dolan, P., Sánchez-Vargas, I., Garcia-Knight, M., Ribiero, I., Chen, T., Olson, K. E., & Andino, R. (2019) · eLife · doi:10.7554/elife.41244 · Cited by 150
piRNAs: biogenesis and their potential roles in cancer
Guo, B., Li, D., Du, L., & Zhu, X. M. (2020) · Cancer and Metastasis Reviews · doi:10.1007/s10555-020-09863-0 · Cited by 140
Weng, W., Li, H., & Goel, A. (2018) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2018.12.005 · Cited by 137
Transcriptional cofactors display specificity for distinct types of core promoters
Haberle, V., Arnold, C. D., Pagani, M., Rath, M., Schernhuber, K., & Stark, A. (2019) · Nature · doi:10.1038/s41586-019-1210-7 · Cited by 123
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Wu, X., Pan, Y., Fang, Y., Zhang, J., Xie, M., Yang, F., Yu, T., Ma, P., Li, W., & Shu, Y. (2020) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2020.05.023 · Cited by 126
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Yamashiro, H., & Siomi, M. C. (2017) · Chemical Reviews · doi:10.1021/acs.chemrev.7b00393 · Cited by 125
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Parhad, S. S., & Theurkauf, W. E. (2019) · Open Biology · doi:10.1098/rsob.180181 · Cited by 103
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Batki, J., Schnabl, J., Wang, J., Handler, D., Andreev, V. I., Stieger, C. E., Novatchkova, M., Lampersberger, L., Kauneckaitė, K., Xie, W., et al. (2019) · Nature Structural & Molecular Biology · doi:10.1038/s41594-019-0270-6 · Cited by 105
Self-citationThe piRNA pathway in Drosophila ovarian germ and somatic cells
Sato, K., & Siomi, M. C. (2020) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.96.003 · Cited by 97
Small RNAs in the Transgenerational Inheritance of Epigenetic Information
Duempelmann, L., Skribbe, M., & Bühler, M. (2020) · Trends in Genetics · doi:10.1016/j.tig.2019.12.001 · Cited by 94
Garland, W., Müller, I. I., Wu, M., Schmid, M., Imamura, K., Rib, L., Sandelin, A., Helin, K., & Jensen, T. H. (2022) · Molecular Cell · doi:10.1016/j.molcel.2022.03.004 · Cited by 97
Gebert, D., Neubert, L. K., Lloyd, C. T., Gui, J., Lehmann, R., & Teixeira, F. K. (2021) · Molecular Cell · doi:10.1016/j.molcel.2021.07.011 · Cited by 89
Heterochromatin as an Important Driver of Genome Organization
Penagos‐Puig, A., & Furlan-Magaril, M. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.579137 · Cited by 92
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Clark, S. L., Hattab, M. W., Chan, R. F., Shabalin, A. A., Han, L. K. M., Zhao, M., Smit, J. H., Jansen, R., Milaneschi, Y., Xie, L. Y., et al. (2019) · Molecular Psychiatry · doi:10.1038/s41380-019-0516-z · Cited by 82
Specialization of the Drosophila nuclear export family protein Nxf3 for piRNA precursor exportPreprint
Kneuss, E., Munafò, M., Eastwood, E. L., Deumer, U.-S., Preall, J. B., Hannon, G. J., & Czech, B. (2019) · Genes & Development · doi:10.1101/gad.328690.119 · Cited by 74
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Luo, S., Zhang, H., Duan, Y., Yao, X., Clark, A. G., & Lü, J. (2020) · BMC Evolutionary Biology · doi:10.1186/s12862-020-1580-3 · Cited by 74
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Zhang, Z., Zhang, J., Diao, L., & Han, L. (2021) · Oncogene · doi:10.1038/s41388-020-01630-3 · Cited by 72
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Parisot, N., Vargas-Chávez, C., Goubert, C., Bâa-Puyoulet, P., Balmand, S., Beranger, L., Blanc, C., Bonnamour, A., Boulesteix, M., Burlet, N., et al. (2021) · BMC Biology · doi:10.1186/s12915-021-01158-2 · Cited by 71
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Olina, A. V., Kulbachinskiy, A. V., Aravin, A. A., & Esyunina, D. (2018) · Biochemistry (Moscow) · doi:10.1134/s0006297918050024 · Cited by 73
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Baumgartner, L., Handler, D., Platzer, S. W., Yu, C., Duchek, P., & Brennecke, J. (2022) · eLife · doi:10.7554/elife.80067 · Cited by 70
Self-citationA guide to the biogenesis and functions of endogenous small non-coding RNAs in animals
Jouravleva, K., & Zamore, P. D. (2025) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-024-00818-9 · Cited by 71
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Liu, J., Ali, M., & Zhou, Q. (2020) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14303 · Cited by 74
Onishi, R., Yamanaka, S., & Siomi, M. C. (2021) · EMBO Reports · doi:10.15252/embr.202153062 · Cited by 64
Hisanaga, T., Romani, F., Wu, S., Kowar, T., Wu, Y., Lintermann, R., Fridrich, A., Cho, C. H., Chaumier, T., Jamge, B., et al. (2023) · Current Biology · doi:10.1016/j.cub.2023.08.073 · Cited by 60
Role of non‑coding RNA in pancreatic cancer (Review)
Lv, Y., & Huang, S. (2019) · Oncology Letters · doi:10.3892/ol.2019.10758 · Cited by 57
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Grentzinger, T., Oberlin, S., Schott, G., Handler, D., Svozil, J., Barragán‐Borrero, V., Humbert, A., Duharcourt, S., Brennecke, J., & Voinnet, O. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa472 · Cited by 54
Self-citationA cascade of bHLH-regulated pathways programs maize anther development
Nan, G.-L., Teng, C., Fernandes, J., O'Connor, L., Meyers, B. C., & Walbot, V. (2022) · The Plant Cell · doi:10.1093/plcell/koac007 · Cited by 51
The burgeoning importance of PIWI-interacting RNAs in cancer progression
Deng, X., Liao, T., Xie, J., Kang, D., He, Y., Sun, Y., Wang, Z., Jiang, Y., Miao, X., Yan, Y., et al. (2023) · Science China Life Sciences · doi:10.1007/s11427-023-2491-7 · Cited by 52
Radion, E., Morgunova, V., Ryazansky, S. S., Akulenko, N. V., Lavrov, S. A., Abramov, Y. A., Komarov, P. A., Glukhov, S. I., Olovnikov, I. A., & Kalmykova, A. I. (2018) · Epigenetics & Chromatin · doi:10.1186/s13072-018-0210-4 · Cited by 50
The birth of piRNAs: how mammalian piRNAs are produced, originated, and evolved
Sun, Y. H., Lee, B., & Li, X. Z. (2021) · Mammalian Genome · doi:10.1007/s00335-021-09927-8 · Cited by 51
RNAi-dependent Polycomb repression controls transposable elements in TetrahymenaPreprint
Zhao, X., Xiong, J., Mao, F., Sheng, Y., Chen, X., Feng, L., Dui, W., Yang, W., Kapusta, A., Feschotte, C., et al. (2019) · Genes & Development · doi:10.1101/gad.320796.118 · Cited by 52
Ravarani, C. N. J., Flock, T., Chavali, S., Anandapadamanaban, M., Babu, M. M., & Santhanam, B. (2020) · Nature Communications · doi:10.1038/s41467-020-16182-z · Cited by 48
Ortolá, B., & Daròs, J. (2024) · Biology · doi:10.3390/biology13030137 · Cited by 51
Chang, T. H., Mattei, E., Gainetdinov, I. V., Colpan, C., Weng, Z., & Zamore, P. D. (2018) · Molecular Cell · doi:10.1016/j.molcel.2018.10.038 · Cited by 48
Osman, K., Yang, J., Roitinger, E., Lambing, C., Heckmann, S., Howell, E. C., Cuacos, M., Imre, R., Dürnberger, G., Mechtler, K., et al. (2017) · The Plant Journal · doi:10.1111/tpj.13752 · Cited by 45
Wei, X., Eickbush, D. G., Speece, I., & Larracuente, A. M. (2021) · eLife · doi:10.7554/elife.62375 · Cited by 44
Beltran, T., Barroso, C., Birkle, T. J. Y., Stevens, L., Schwartz, H. T., Sternberg, P. W., Fradin, H., Gunsalus, K. C., Piano, F., Sharma, G., et al. (2019) · Developmental Cell · doi:10.1016/j.devcel.2018.12.026 · Cited by 46
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Santos, D., Feng, M., Κολλιοπούλου, Ά., Taning, C. N. T., Sun, J., & Swevers, L. (2023) · Insects · doi:10.3390/insects14020187 · Cited by 46
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Sun, Y. H., Zhu, J., Xie, L. H., Li, Z., Meduri, R., Zhu, X., Song, C. W., Chen, C., Ricci, E. P., Weng, Z., et al. (2020) · Nature Cell Biology · doi:10.1038/s41556-019-0457-4 · Cited by 42
Silence at the End: How Drosophila Regulates Expression and Transposition of Telomeric Retroelements
Cacchione, S., Cenci, G., & Raffa, G. D. (2020) · Journal of Molecular Biology · doi:10.1016/j.jmb.2020.06.004 · Cited by 44
Chen, P., Luo, Y., & Aravin, A. A. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009591 · Cited by 42
Functions of HP1 proteins in transcriptional regulation
Schoelz, J. M., & Riddle, N. C. (2022) · Epigenetics & Chromatin · doi:10.1186/s13072-022-00453-8 · Cited by 41
Arabidopsis DXO1 links RNA turnover and chloroplast function independently of its enzymatic activity
Kwaśnik, A., Wang, V. Y., Krzysztoń, M., Gozdek, A., Zakrzewska‐Placzek, M., Stępniak, K., Poznański, J. T., Tong, L., & Kufel, J. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz100 · Cited by 42
The USTC co-opts an ancient machinery to drive piRNA transcription in C. elegansPreprint
Weng, C., Kosalka, J., Berkyurek, A. C., Stempor, P., Feng, X., Mao, H., Zeng, C., Li, W.-J., Yan, Y.-H., Dong, M.-Q., et al. (2018) · Genes & Development · doi:10.1101/gad.319293.118 · Cited by 44
Critical appraisal of the piRNA-PIWI axis in cancer and cancer stem cells
Garcia‐Borja, E., Siegl, F., Mateu, R., Slabý, O., Šedo, A., Bušek, P., & Šáňa, J. (2024) · Biomarker Research · doi:10.1186/s40364-024-00563-3 · Cited by 41
Learning deep features and topological structure of cells for clustering of scRNA-sequencing data
Wang, H., & Ma, X. (2022) · Briefings in Bioinformatics · doi:10.1093/bib/bbac068 · Cited by 40
Weiser, N. E., & Kim, J. K. (2019) · Annual Review of Genetics · doi:10.1146/annurev-genet-112618-043505 · Cited by 42
Yu, T., Fan, K., Özata, D. M., Zhang, G., Fu, Y., Theurkauf, W. E., Zamore, P. D., & Weng, Z. (2021) · Nature Communications · doi:10.1038/s41467-020-20345-3 · Cited by 42
Maternally inherited siRNAs initiate piRNA cluster formation
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Casier, K., Boivin, A., Carré, C., & Teysset, L. (2019) · Cells · doi:10.3390/cells8091108 · Cited by 37
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Anti-silencing factor Epe1 associates with SAGA to regulate transcription within heterochromatinPreprint
Bao, K., Shan, C., Moresco, J. J., Yates, J. R., & Jia, S. (2018) · Genes & Development · doi:10.1101/gad.318030.118 · Cited by 36
Environmentally-induced epigenetic conversion of a piRNA cluster
Casier, K., Delmarre, V., Gueguen, N., Hermant, C., Viodé, E., Vaury, C., Ronsseray, S., Brasset, É., Teysset, L., & Boivin, A. (2019) · eLife · doi:10.7554/elife.39842 · Cited by 35
Transcriptional and chromatin changes accompanying de novo formation of transgenic piRNA clusters
Akulenko, N. V., Ryazansky, S. S., Morgunova, V., Komarov, P. A., Olovnikov, I. A., Vaury, C., Jensen, S., & Kalmykova, A. I. (2018) · RNA · doi:10.1261/rna.062851.117 · Cited by 34
The emerging role of non-coding RNAs in the epigenetic regulation of pediatric cancers
Pathania, A. S., Prathipati, P., Pandey, M. K., Byrareddy, S. N., Coulter, D. W., Gupta, S. C., & Challagundla, K. B. (2021) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2021.04.015 · Cited by 35
van Lopik, J., Alizada, A., Trapotsi, M., Hannon, G. J., Bornelöv, S., & Czech, B. (2023) · Nature Communications · doi:10.1038/s41467-023-42787-1 · Cited by 33
Co-dependent Assembly of Drosophila piRNA Precursor Complexes and piRNA Cluster Heterochromatin
Zhang, G., Tu, S., Yu, T., Zhang, X.-O., Parhad, S. S., Weng, Z., & Theurkauf, W. E. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.08.081 · Cited by 34
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Kordyukova, M., Sokolova, O. A., Morgunova, V., Ryazansky, S. S., Akulenko, N. V., Glukhov, S. I., & Kalmykova, A. I. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz1072 · Cited by 31
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Wierzbicki, F., Kofler, R., & Signor, S. A. (2021) · Molecular Ecology · doi:10.1111/mec.16311 · Cited by 31
Théron, E., Maupetit‐Mehouas, S., Pouchin, P., Baudet, L., Brasset, É., & Vaury, C. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky695 · Cited by 32
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Riquelme, I., Pérez, P. E., Letelier, P. J., Brebi, P., & Roa, J. C. (2021) · Cancers · doi:10.3390/cancers14010202 · Cited by 31
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de Brito, T. F., Julio, A. H. F., Berni, M. A., Poncio, L. D. C., Bernardes, E. S., Araujo, H. M., Sammeth, M., & Pane, A. (2018) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0006760 · Cited by 27
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Munafò, M., Lawless, V. R., Passera, A., MacMillan, S., Bornelöv, S., Haussmann, I. U., Soller, M., Hannon, G. J., & Czech, B. (2021) · eLife · doi:10.7554/elife.66321 · Cited by 27
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Metadata
- Authors
- Andersen, P. R., Tirian, L., Vunjak, M., & Brennecke, J.
- Affiliations
- Institute of Molecular Biotechnology (AT)
- Corresponding author
- Andersen, Peter Refsing
- Brennecke, Julius
- Venue
- Nature
- Published
- 2017-08-23
- Volume
- 549
- Issue
- 7670
- Pages
- 54-59
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC5590728
- OpenAlex
- W2748864067
- Cited by
- 280
- References
- 78
- Citations by year
- 2026: 20 · 2025: 32 · 2024: 39 · 2023: 37 · 2022: 21 · 2021: 35 · 2020: 25 · 2019: 37 · 2018: 27 · 2017: 6
- FWCI
- 10.62
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Novo Nordisk Fonden (NNF14OC0009189)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Chromosomal and Genetic Variations
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Keywords
- piRNA, heterochromatin, rhinoceros, HP1, TRF2, TFIID, transposon silencing, germline, Drosophila, histone modifications, genome stability
- MeSH terms
- Animals, Chromosomal Proteins, Non-Histone, DNA Transposable Elements, Drosophila melanogaster, Female, Multigene Family, Heterochromatin, Promoter Regions, Genetic, RNA Polymerase II, Transcription, Genetic, Gene Silencing, Drosophila Proteins, RNA, Small Interfering, Telomeric Repeat Binding Protein 2, Transcription Factor TFIIA, Transcription Initiation, Genetic
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