bioRxivEvolutionary BiologyPreprint
Insect metamorphosis is regulated differently between sexes by members of a microRNA cluster
Chade Li, Ki Kei ChaniD, Wenyan NongiD, ShanShan CheniD, Wai Lok SoiD, Zhe QuiD, Heidi Y.C. Wu, Ho Yin YipiD, Chi Bun ChaniD, Stephen S. TobeiD, William G. BendenaiD, Zhen‐peng KaiiD, Jerome H. L. HuiiD
Abstract
Insects comprise the majority of all described animal species and dominate the terrestrial habitats. The evolution of insect metamorphosis played a profound role in their successful adaptation and radiation. Insect metamorphosis is dependent on hormones ecdysteroids and sesquiterpenoids such as juvenile hormone. Despite the fact there are genuine differences between sexes during insect metamorphosis which facilitate their successful mating, how such sexual dimorphism in metamorphosis is being controlled is poorly known. We first generated transcriptomic profiles of male and female flies in late larvae and early pupae stages. Using a combination of genome-wide prediction and in vitro dual-luciferase validations, members of a microRNA cluster miR-277/34 were found to potentially regulate the neuropeptide receptor (AstC-R1) that when activated inhibits the sesquiterpenoid pathway and a juvenile hormone-dependent transcription factor (Kr-h1) in fly Drosophila melanogaster. Loss-of-function mutants were created deleting either miR-277 or miR-34, and expression levels of both AstC-R1 and Kr-h1 as well as ecdysteroid and sesquiterpenoid hormone titres were altered. Further comparison of transcriptomes of the late larvae and early pupae of both sexes revealed differential gene pathways being regulated by members of miR-277/34 between sexes during metamorphosis. This study highlights how members of a microRNA cluster control hormonal and developmental gene pathways in different sexes of insects during metamorphosis.
- organism: Drosophila
- assay: bulk RNA-seq
- research focus: cell type annotation
- research focus: differential expression
- approach: genetic perturbation / CRISPR
- Citations
- 1
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