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Silencing cuticular pigmentation genes enables RNA FISH in intact insect appendages.

Stefan PentzoldVeit GrabeAndrei OgonkovLydia SchmidtWillhelm BolandAntje Burse
Published in: The Journal of experimental biology (2018)
Optical imaging of gene expression by fluorescence in situ hybridisation (FISH) in insects is often impeded by their pigmented cuticle. As most chemical bleaching agents are incompatible with FISH, we developed an RNA interference (RNAi)-based method for clearing cuticular pigmentation which enables the use of whole-mount body appendages for RNA FISH (termed RNA-i-FISH). Silencing laccase2 or tyrosine hydroxylase in two leaf beetles species (Chrysomela populi and Phaedon cochleariae) cleared their pigmented cuticle and decreased light absorbance. Subsequently, intact appendages (palps, antennae, legs) from RNAi-cleared individuals were used to image the expression and spatial distribution of antisense mRNA of two chemosensory genes encoding gustatory receptor and odorant-binding protein. Imaging did not work for RNAi controls because the pigmentation was retained, or for FISH controls (sense mRNA). Several bleaching agents were incompatible with FISH, because of degradation of RNA, lack of clearing efficacy or long incubation times. Overall, silencing pigmentation genes is a significant improvement over bleaching agents, enabling FISH in intact insect appendages.
Keyphrases
  • binding protein
  • gene expression
  • high resolution
  • hydrogen peroxide
  • nucleic acid
  • deep learning
  • mass spectrometry
  • energy transfer
  • basal cell carcinoma