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Select item 111075441.

Silencing transposable elements in the Drosophila germline

Fu Yang, Rongwen Xi

Cell Mol Life Sci. 2017 Feb; 74(3): 435–448. Published online 2016 Sep 6. doi: 10.1007/s00018-016-2353-4

PMCID:: PMC11107544

Abstract Article PDF–1.3M

Select item 87334202.

A genetic toolkit for studying transposon control in the Drosophila melanogaster ovary

Mostafa F ElMaghraby, Laszlo Tirian, Kirsten-André Senti, Katharina Meixner, Julius Brennecke

Genetics. 2022 Jan; 220(1): iyab179. Published online 2021 Oct 30. doi: 10.1093/genetics/iyab179

PMCID:: PMC8733420

Abstract Article PDF–3.3M

Select item 77852503.

Telomeric TART elements target the piRNA machinery in Drosophila

Christopher E. Ellison, Meenakshi S. Kagda, Weihuan Cao

PLoS Biol. 2020 Dec; 18(12): e3000689. Published online 2020 Dec 21. doi: 10.1371/journal.pbio.3000689

PMCID:: PMC7785250

Abstract Article PDF–2.4M

Select item 76011714.

Diverse Defenses: A Perspective Comparing Dipteran Piwi-piRNA Pathways

Stephanie Gamez, Satyam Srivastav, Omar S. Akbari, Nelson C. Lau

Cells. 2020 Oct; 9(10): 2180. Published online 2020 Sep 27. doi: 10.3390/cells9102180

PMCID:: PMC7601171

Abstract Article PDF–2.4M

Select item 73371855.

piRNA and Transposon Dynamics in Drosophila: A Female Story

Bastien Saint-Leandre, Pierre Capy, Aurelie Hua-Van, Jonathan Filée

Genome Biol Evol. 2020 Jun; 12(6): 931–947. Published online 2020 May 12. doi: 10.1093/gbe/evaa094

PMCID:: PMC7337185

Abstract Article PDF–1.6M

Select item 70015046.

Armitage determines Piwi−piRISC processing from precursor formation and quality control to inter‐organelle translocation

Haruna Yamashiro, Mayu Negishi, Tatsuki Kinoshita, Hirotsugu Ishizu, Hitoshi Ohtani, Mikiko C Siomi

EMBO Rep. 2020 Feb 5; 21(2): e48769. Published online 2019 Dec 12. doi: 10.15252/embr.201948769

PMCID:: PMC7001504

Abstract Article PDF–1.0M

Select item 69744057.

The piRNA pathway in Drosophila ovarian germ and somatic cells

Kaoru SATO, Mikiko C. SIOMI

Proc Jpn Acad Ser B Phys Biol Sci. 2020 Jan 10; 96(1): 32–42. doi: 10.2183/pjab.96.003

PMCID:: PMC6974405

Abstract Article PDF–2.3M

Select item 69584398.

Assembly and Function of Gonad-Specific Non-Membranous Organelles in Drosophila piRNA Biogenesis

Shigeki Hirakata, Mikiko C. Siomi

Noncoding RNA. 2019 Dec; 5(4): 52. Published online 2019 Nov 6. doi: 10.3390/ncrna5040052

PMCID:: PMC6958439

Abstract Article PDF–1.6M

Select item 66363569.

The RNA-binding ATPase, Armitage, Couples piRNA Amplification in Nuage to Phased piRNA Production on Mitochondria

Daniel Tianfang Ge, Wei Wang, Cindy Tipping, Ildar Gainetdinov, Zhiping Weng, Phillip D. Zamore

Mol Cell. Author manuscript; available in PMC 2020 Jun 6.

Published in final edited form as: Mol Cell. 2019 Jun 6; 74(5): 982–995.e6. Published online 2019 May 7. doi: 10.1016/j.molcel.2019.04.006

PMCID:: PMC6636356

Abstract Article PDF–1.4M

Select item 660150710.

Daedalus and Gasz recruit Armitage to mitochondria, bringing piRNA precursors to the biogenesis machinery

Marzia Munafò, Vera Manelli, Federica A. Falconio, Ashley Sawle, Emma Kneuss, Evelyn L. Eastwood, Jun Wen Eugene Seah, Benjamin Czech, Gregory J. Hannon

Genes Dev. 2019 Jul 1; 33(13-14): 844–856. doi: 10.1101/gad.325662.119

PMCID:: PMC6601507

Abstract Article PDF–6.6M

Select item 570780511.

Landscape and evolution of tissue-specific alternative polyadenylation across Drosophila species

Piero Sanfilippo, Jiayu Wen, Eric C. Lai

Genome Biol. 2017; 18: 229. Published online 2017 Nov 30. doi: 10.1186/s13059-017-1358-0

PMCID:: PMC5707805

Abstract Article PDF–3.2M

Select item 568900212.

Transcription elongation rate has a tissue-specific impact on alternative cleavage and polyadenylation in Drosophila melanogaster

Xiaochuan Liu, Jaime Freitas, Dinghai Zheng, Marta S. Oliveira, Mainul Hoque, Torcato Martins, Telmo Henriques, Bin Tian, Alexandra Moreira

RNA. 2017 Dec; 23(12): 1807–1816. doi: 10.1261/rna.062661.117

PMCID:: PMC5689002

Abstract Article PDF–4.0M

Select item 548753313.

Silencing of Transposable Elements by piRNAs in Drosophila: An Evolutionary Perspective

Shiqi Luo, Jian Lu

Genomics Proteomics Bioinformatics. 2017 Jun; 15(3): 164–176. Published online 2017 Jun 8. doi: 10.1016/j.gpb.2017.01.006

PMCID:: PMC5487533

Abstract Article PDF–1.2M

Select item 515964314.

Kc167, a widely used Drosophila cell line, contains an active primary piRNA pathway

Nicholas Vrettos, Manolis Maragkakis, Panagiotis Alexiou, Zissimos Mourelatos

RNA. 2017 Jan; 23(1): 108–118. doi: 10.1261/rna.059139.116

PMCID:: PMC5159643

Abstract Article PDF–566K

Select item 488965815.

mRNA-Associated Processes and Their Influence on Exon-Intron Structure in Drosophila melanogaster

Gildas Lepennetier, Francesco Catania

G3 (Bethesda) 2016 Jun; 6(6): 1617–1626. Published online 2016 Mar 28. doi: 10.1534/g3.116.029231

PMCID:: PMC4889658

Abstract Article PDF–1.5M

Select item 456802516.

Genes conserved in bilaterians but jointly lost with Myc during nematode evolution are enriched in cell proliferation and cell migration functions

Albert J. Erives

Dev Genes Evol. 2015; 225(5): 259–273. Published online 2015 Jul 15. doi: 10.1007/s00427-015-0508-1

PMCID:: PMC4568025

Abstract Article PDF–2.8M

Select item 456084217.

Slicing and Binding by Ago3 or Aub Trigger Piwi-bound piRNA Production by Distinct Mechanisms

Wei Wang, Bo W. Han, Cindy Tipping, Daniel Tianfang Ge, Zhao Zhang, Zhiping Weng, Phillip D. Zamore

Mol Cell. Author manuscript; available in PMC 2016 Sep 3.

Published in final edited form as: Mol Cell. 2015 Sep 3; 59(5): 819–830. doi: 10.1016/j.molcel.2015.08.007

PMCID:: PMC4560842

Abstract Article PDF–2.8M

Select item 454529118.

piRNA-Guided Transposon Cleavage Initiljates Zucchini-Dependent, Phased piRNA Production

Bo W Han, Wei Wang, Chengjian Li, Zhiping Weng, Phillip D. Zamore

Science. Author manuscript; available in PMC 2015 Nov 15.

Published in final edited form as: Science. 2015 May 15; 348(6236): 817–821. doi: 10.1126/science.aaa1264

PMCID:: PMC4545291

Abstract Article PDF–635K

Select item 452833019.

Gene Model Annotations for Drosophila melanogaster: The Rule-Benders

Madeline A. Crosby, L. Sian Gramates, Gilberto dos Santos, Beverley B. Matthews, Susan E. St. Pierre, Pinglei Zhou, Andrew J. Schroeder, Kathleen Falls, David B. Emmert, Susan M. Russo, William M. Gelbart, the FlyBase Consortium

G3 (Bethesda) 2015 Aug; 5(8): 1737–1749. Published online 2015 Jun 24. doi: 10.1534/g3.115.018937

PMCID:: PMC4528330

Abstract Article PDF–2.2M

Select item 452832920.

Gene Model Annotations for Drosophila melanogaster: Impact of High-Throughput Data

Beverley B. Matthews, Gilberto dos Santos, Madeline A. Crosby, David B. Emmert, Susan E. St. Pierre, L. Sian Gramates, Pinglei Zhou, Andrew J. Schroeder, Kathleen Falls, Victor Strelets, Susan M. Russo, William M. Gelbart, the FlyBase Consortium

G3 (Bethesda) 2015 Aug; 5(8): 1721–1736. Published online 2015 Jun 24. doi: 10.1534/g3.115.018929