Drosophila Piwi distinguishes transposons from mRNAs by piRNA complementarity and abundance

Piwi-interacting RNAs (piRNAs) are the main repressors of transposable elements (TEs) in animal germlines. In Drosophila, Piwi-piRNA complexes associate with nascent TE transcripts to drive heterochromatin formation and TE repression. However, previous studies have shown that Piwi also associates with large numbers of mRNAs, raising the question of how Piwi discriminates between mRNAs and TEs. To answer this question, we performed a comprehensive analysis of Piwi-associated RNAs, compositionally and functionally, to decipher the targeting rules of Piwi-piRNA complexes. While Piwi initially identifies its targets through the seed sequence, it requires pairing well beyond the seed, nearly a perfect match, to elicit a repressive response. In addition to the complementarity of piRNAs to their targets, their abundance must reach a certain threshold to be functional. Together, these findings explain large differences in the target repression of Piwi-associated RNAs and reveal how Piwi efficiently distinguishes TEs from mRNAs despite associating with both.

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Publication Details

Journal
Cell Reports
Published
2024-12-01
DOI
https://doi.org/10.1016/j.celrep.2024.115020
Citations
6
Primary Topic
Chromosomal and Genetic Variations
Type
article
Field-Weighted Citation Impact
3.60

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article

Drosophila Piwi distinguishes transposons from mRNAs by piRNA complementarity and abundance

Haruhiko Siomi, Hazuki Takahashi, Yuka W. Iwasaki, Piero Carninci et al.
6 citations
Cell Reports
Chromosomal and Genetic Variations
3.60
article

Drosophila Piwi distinguishes transposons from mRNAs by piRNA complementarity and abundance

Haruhiko Siomi, Hazuki Takahashi, Yuka W. Iwasaki, Piero Carninci, Therese Solberg, Masaru Ariura, Hirotsugu Ishizu
article en
6 citations

Abstract

Piwi-interacting RNAs (piRNAs) are the main repressors of transposable elements (TEs) in animal germlines. In Drosophila, Piwi-piRNA complexes associate with nascent TE transcripts to drive heterochromatin formation and TE repression. However, previous studies have shown that Piwi also associates with large numbers of mRNAs, raising the question of how Piwi discriminates between mRNAs and TEs. To answer this question, we performed a comprehensive analysis of Piwi-associated RNAs, compositionally and functionally, to decipher the targeting rules of Piwi-piRNA complexes. While Piwi initially identifies its targets through the seed sequence, it requires pairing well beyond the seed, nearly a perfect match, to elicit a repressive response. In addition to the complementarity of piRNAs to their targets, their abundance must reach a certain threshold to be functional. Together, these findings explain large differences in the target repression of Piwi-associated RNAs and reveal how Piwi efficiently distinguishes TEs from mRNAs despite associating with both.

Cell ReportsVol. 43(12)
Keio University (JP), Human Technopole (IT), RIKEN Center for Integrative Medical Sciences (JP)
Japan Agency for Medical Research and Development, Ministry of Education, Culture, Sports, Science and Technology, Japan Society for the Promotion of Science, Japan Science and Technology Agency
Zero hunger
Openalex Percentile: Top 7%
Chromosomal and Genetic Variations
3.60
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Drosophila Piwi distinguishes transposons from mRNAs by piRNA complementarity and abundance — Haruhiko Siomi, Hazuki Takahashi, et al. · Cell Reports (2024) | TGRS Research Map | TGRS