Abstract
Piwi proteins and their bound Piwi-interacting RNAs (piRNAs) are predominantly expressed in the germline and play crucial roles in germline development by silencing transposons and other targets. Bombyx mori BmN4 cells are culturable germ cells that equip the piRNA pathway. Because of the scarcity of piRNA-expressing culturable cells, BmN4 cells are being utilized for the analyses of piRNA biogenesis. We here report that the piRNA biogenesis in BmN4 cells is regulated by cell density. As cell density increased, the abundance of Piwi proteins and piRNA biogenesis factors was commonly upregulated, resulting in an increased number of perinuclear nuage-like granules where Piwi proteins localize. Along with these phenomena, the abundance of mature piRNAs also globally increased, whereas levels of long piRNA precursor and transposons decreased, suggesting that increasing cell density promotes piRNA biogenesis pathway and that the resultant accumulation of mature piRNAs is functionally significant for transposon silencing. Our study reveals a previously uncharacterized link between cell density and piRNA biogenesis, designates cell density as a critical variable in piRNA studies using BmN4 cell system, and suggests the alteration of cell density as a useful tool to monitor piRNA biogenesis and function.
Highlights
Piwi proteins and their bound Piwi-interacting RNAs are abundantly expressed in animal germlines to regulate transposable elements and other targets such as germline mRNAs1–3
The abundance of Piwi proteins and Piwi-interacting RNAs (piRNAs) biogenesis factors is linked to cell density
During the course of investigating the piRNA pathway using BmN4 cells, we noticed that the levels of Piwi proteins and piRNAs differed in cells with varying densities
Summary
Piwi proteins and their bound Piwi-interacting RNAs (piRNAs) are abundantly expressed in animal germlines to regulate transposable elements and other targets such as germline mRNAs1–3. BmN4 cells are the only reported germ cells that express an endogenous piRNA pathway. We investigated the expression levels of Piwi proteins and other piRNA biogenesis protein factors, piRNA precursor, mature piRNAs, and transposons in the cells with different densities. The obtained results collectively suggest that increasing cell density promotes piRNA biogenesis and that the resultant accumulation of mature piRNAs is functionally significant for transposon silencing. These results reveal a previously uncharacterized link between cell density and piRNA biogenesis, uncovering a critical parameter that should be taken into consideration in piRNA studies. Our results suggest that the alteration of BmN4 cell density should provide a useful tool to monitor piRNA biogenesis and function
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