Abstract

BackgroundPIWI-interacting RNAs (piRNAs) are the effectors of transposable element silencing in the reproductive apparatus. In Drosophila ovarian somatic cells, piRNAs arise from long RNA precursors presumably processed within cytoplasmic Yb-bodies.ResultsHere we show that the nucleo-cytoplasmic traffic of piRNA precursors encoded by the flamenco locus is subjected to a spatio-temporal regulation. Precursor RNAs first gather in a single nuclear focus, Dot COM, close to the nuclear periphery, and transit through the membrane before being delivered to the cytoplasmic Yb-bodies. Early in oogenesis, flamenco transcripts are rapidly transferred to the cytoplasm making their initial nuclear gathering in Dot COM too transient to be visualized. As oogenesis proceeds, the cytoplasmic delivery steadily decreases concomitantly with the decrease in the protein levels of Armi and Yb, two components of the Yb-bodies. Both events lead to a reduction of Yb-body assembly in late stages of oogenesis, which likely results in a drop in piRNA production.ConclusionOur findings show a spatio-temporal regulation of the piRNA biogenesis in the follicle cells of Drosophila ovaries, that involves coordinated control of both piRNA precursors and components of the piRNA processing machinery. This newly unveiled regulation establishes another level of complexity in the production of piRNAs and suggests a stage-dependent involvement of the piRNA biogenesis in the mechanism of transposable elements silencing along oogenesis.

Highlights

  • PIWI-interacting RNAs are the effectors of transposable element silencing in the reproductive apparatus

  • Mature PIWI-interacting RNAs (piRNAs) associated with Piwi protein form a piRNA-induced silencing complex that is delivered to the nucleus to target nascent transposable elements (TEs) mRNAs and initiate transcriptional gene silencing [11, 12]

  • Depending on the follicle cell observed, the focus where flam precursors gathered was visualized either completely within the nucleus close to the nuclear periphery, or stretching across the nuclear membrane, or within the cytoplasm close to the nuclear membrane. To investigate whether this differential localization is somehow related to the stage of the developing egg chambers, we examined flam RNA precursors in follicle cells within egg chambers in stages 3 to 10 of oogenesis

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Summary

Introduction

PIWI-interacting RNAs (piRNAs) are the effectors of transposable element silencing in the reproductive apparatus. In the gonads, where it is essential to ensure the maintenance of genome integrity for the generation, the piRNA pathway is responsible for TE silencing in both somatic and germinal tissues [1,2,3,4] This process involves small guide piRNAs of 23–29. 142 piRNA clusters have been identified in Drosophila melanogaster [2], mostly located in pericentromeric and telomeric regions These clusters vary considerably in size from a few kilobases (kb) to several hundred kb. Flam transcripts undergo alternative splicing to generate diverse piRNA precursors that all share the first exon at their 5′ end [8] These transcripts are processed into 23–29 nt piRNAs, presumably in cytoplasmic Yb-bodies [9, 10]. Mature piRNAs associated with Piwi protein form a piRNA-induced silencing complex (piRISC) that is delivered to the nucleus to target nascent TE mRNAs and initiate transcriptional gene silencing [11, 12]

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