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Insects exhibit diverse developmental strategies, yet the molecular basis of sexual dimorphism in metamorphosis remains largely elusive. The white wax scale insect Ericerus pela (hereafter, WWS) displays extreme sexual dimorphism: females undergo paurometamorphosis (four stages), while males undergo hyperpaurometamorphosis (five stages). Although miR-277 is highly expressed in both sexes, its functional role in this process was unknown. Here, we demonstrate that miR-277 drives sexually dimorphic development through differential regulation of two distinct targets. Combining gain- and loss-of-function assays, dual-luciferase reporter assays, and RNA interference, we show that miR-277 suppresses Discs large 1 (Dlg1) in females, disrupting cellular signaling and causing growth retardation and morphological abnormalities. In males, miR-277 inhibits tyrosine-protein phosphatase Lar (Lar), a receptor tyrosine phosphatase linked to nervous system development; knockdown of Lar severely impairs male metamorphosis but does not affect females. These findings reveal a previously unrecognized, sex-specific miRNA regulatory switch: miR-277 concurrently modulates a cell-growth pathway in females and a neurodevelopmental pathway in males, thereby generating divergent developmental outcomes. Our study provides the mechanistic insight into miRNA-mediated sexual dimorphism in insects and advances the understanding of how post-transcriptional regulators shape metamorphic diversity.
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Chen et al. (2026) studied this question.
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