Drosophila Piwi functions downstream of piRNA production mediating a chromatin-based transposon silencing mechanism in female germ line
Open accessAbstract
Transposon control is a critical process during reproduction. The PIWI family proteins can play a key role, using a piRNA-mediated slicing mechanism to suppress transposon activity posttranscriptionally. In Drosophila melanogaster , Piwi is predominantly localized in the nucleus and has been implicated in heterochromatin formation. Here, we use female germ-line–specific depletion to study Piwi function. This depletion of Piwi leads to infertility and to axis specification defects in the developing egg chambers; correspondingly, widespread loss of transposon silencing is observed. Germ-line Piwi does not appear to be required for piRNA production. Instead, Piwi requires Aubergine (and presumably secondary piRNA) for proper localization. A subset of transposons that show significant overexpression in germ-line Piwi-depleted ovaries exhibit a corresponding loss of HP1a and H3K9me2. Germ-line HP1a depletion also leads to a loss of transposon silencing, demonstrating the functional requirement for HP1a enrichment at these loci. Considering our results and those of others, we infer that germ-line Piwi functions downstream of piRNA production to promote silencing of some transposons via recruitment of HP1a. Thus, in addition to its better-known function in posttranscriptional silencing, piRNA also appears to function in a targeting mechanism for heterochromatin formation mediated by Piwi.
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Piwi and piRNAs are most abundant in the germline, where they play a key role in retrotransposon silencing at the RNA and chromatin levels.
“Piwi and piRNAs are most abundant in the germline, where they play a key role in retrotransposon silencing at the RNA and chromatin levels”
From The Role of Retrotransposons and Endogenous Retroviruses in Age-Dependent Neurodegenerative Disorders (2024) · cites this paper as Wang & Elgin 2011
The Abstract describes piRNA-mediated posttranscriptional transposon silencing, and the Discussion reports evidence for a chromatin-based mechanism involving germ-line Piwi. However, the paper does not establish that Piwi and piRNAs are most abundant in the germ line; the Abstract also describes Piwi and piRNA pathways in the ovarian soma. Its findings concern transposons, without establishing that both mechanisms apply specifically to retrotransposons. (LLM, conf=0.86)
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<i>Drosophila</i> PIWI associates with chromatin and interacts directly with HP1a
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Silencio/CG9754 connects the Piwi-piRNA complex to the cellular heterochromatin machinery
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- Authors
- Wang, S. H., & Elgin, S. C. R.
- Affiliations
- Washington University in St. Louis (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2011-12-12
- Volume
- 108
- Issue
- 52
- Pages
- 21164-21169
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC3248523
- OpenAlex
- W2034161629
- Cited by
- 232
- References
- 2
- Citations by year
- 2026: 5 · 2025: 11 · 2024: 6 · 2023: 14 · 2022: 7 · 2021: 28 · 2020: 11 · 2019: 11 · 2018: 18 · 2017: 13 · 2016: 15 · 2015: 22 · 2014: 26 · 2013: 31 · 2012: 13
- FWCI
- 27.00
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Open Scholarship Institutional Repository (Washington University in St. Louis) (submittedVersion)
- Funders
- National Institute of General Medical Sciences (R01GM073190, R01GM068388, GM068388, GM073190)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Chromosomal and Genetic Variations
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Keywords
- Piwi, piRNA, transposon silencing, female germline, heterochromatin formation, HP1α, H3K9me2, eggplant, infertility, Drosophila melanogaster
- MeSH terms
- Chromobox Protein Homolog 5, Animals, Chromosomal Proteins, Non-Histone, DNA Transposable Elements, Drosophila melanogaster, Female, Germ Cells, Heterochromatin, Blotting, Northern, Blotting, Western, DNA Primers, Microscopy, Confocal, Drosophila Proteins, RNA Interference, RNA, Small Interfering, Chromatin Immunoprecipitation, Argonaute Proteins, Real-Time Polymerase Chain Reaction
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